Anatomy and Physiology of the Integumentary System (PDF)

1. Functions of the Integumentary System 1. Physical Protection: ○ The skin acts as a mechanical barrier, preventing the entry of pathogens and protecting against physical injury, chemicals, and radiation. The stratum corneum, composed of dead keratinized cells, forms a tough, protective layer that resists abrasion and penetration by microbes. 2. Vitamin D Synthesis: ○ UVB rays convert 7-dehydrocholesterol in the epidermis into previtamin D3, which is then converted to cholecalciferol (Vitamin D3). This molecule undergoes hydroxylation in the liver to form calcidiol and then in the kidneys to form the active hormone calcitriol. Calcitriol is essential for calcium and phosphate homeostasis, promoting bone mineralization and modulating immune function. 3. Sensation: ○ The skin houses a variety of sensory receptors, including: Meissner’s Corpuscles for light touch. Pacinian Corpuscles for deep pressure and vibration. Ruffini Endings for skin stretch and sustained pressure. Merkel Cells for fine touch and texture discrimination. Nociceptors for pain, which respond to harmful stimuli such as extreme temperatures and mechanical damage. Thermoreceptors for detecting changes in temperature. 4. Excretion: ○ Through eccrine sweat glands, the skin excretes small amounts of metabolic waste products, including urea, uric acid, and ammonia, helping to maintain homeostasis. 5. Temperature Regulation: ○ The skin regulates body temperature through mechanisms such as: Vasodilation: Blood vessels in the dermis dilate to increase blood flow to the skin surface, facilitating heat loss. Vasoconstriction: Blood vessels constrict to reduce blood flow and retain heat. Sweating: Eccrine glands secrete sweat, which evaporates to cool the body. Apocrine glands, found in areas such as the armpits and groin, release a thicker sweat under stress or sexual stimulation. 6. Innate Immunity: ○ The skin serves as a primary defense against pathogens through: Physical Barrier: The tightly packed keratinized cells prevent pathogen entry. Chemical Barrier: Sebum and sweat create an acidic environment (pH 4.5-5.5) that inhibits bacterial growth. Cellular Immunity: Langerhans cells, located in the stratum spinosum, act as antigen-presenting cells, initiating immune responses. 2. Anatomy and Histological Characteristics of the Layers of the Skin 1. Epidermis: ○ Stratum Corneum: The outermost layer consisting of dead keratinized cells. It acts as a waterproof barrier and protects against microbial invasion and environmental damage. ○ Stratum Lucidum: Found only in thick skin, this thin, clear layer of dead cells provides an additional barrier. ○ Stratum Granulosum: Contains keratinocytes with keratohyalin granules that contribute to the formation of the keratin layer. Cells in this layer are undergoing apoptosis. ○ Stratum Spinosum: Several layers of keratinocytes connected by desmosomes, giving a spiny appearance. This layer provides structural strength and flexibility. ○ Stratum Basale (Germinativum): A single layer of mitotically active stem cells that produce new keratinocytes. It also contains melanocytes and Merkel cells. 2. Dermis: ○ Papillary Layer: Composed of loose areolar connective tissue, this layer contains dermal papillae that interlock with the epidermis, increasing surface area for nutrient exchange. It houses capillaries, pain receptors, and Meissner’s corpuscles. ○ Reticular Layer: Made of dense irregular connective tissue, providing structural strength. It contains collagen and elastin fibers, as well as hair follicles, sebaceous and sweat glands, blood vessels, and nerve endings. 3. Hypodermis (Subcutaneous Layer): ○ Composed of adipose tissue and loose connective tissue, the hypodermis anchors the skin to underlying tissues, provides insulation and cushioning, and serves as an energy reserve. It also contains large blood vessels and nerves. 3. Anatomy and Histological Characteristics of the Component Parts of the Skin 1. Hair: ○ Structure: Hair Shaft: The visible part of the hair above the skin surface. It consists of the medulla, cortex, and cuticle. Hair Follicle: A tubular invagination of the epidermis extending into the dermis and hypodermis. The follicle is surrounded by an outer and inner root sheath. Hair Bulb: The base of the follicle containing the matrix, where cell division occurs, and the dermal papilla, which supplies nutrients. ○ Growth Cycle: Anagen Phase: Active growth phase where cells in the hair matrix rapidly divide. Catagen Phase: Transitional phase where growth slows, and the follicle shrinks. Telogen Phase: Resting phase where the hair is shed, and the follicle remains dormant before a new cycle begins. 2. Nails: ○ Made of hard keratin. The nail matrix, located at the base of the nail, is responsible for producing new nail cells. ○ Nail Plate: The hard, visible part of the nail. ○ Nail Bed: Skin beneath the nail plate that provides nourishment. ○ Cuticle (Eponychium): A protective barrier at the base of the nail plate. 3. Integumentary Glands: ○ Eccrine Sweat Glands: Found all over the body, especially on palms and soles. They produce a watery sweat that helps in thermoregulation. ○ Apocrine Sweat Glands: Located in the axillae and groin. They produce a thicker, protein-rich sweat, which bacteria break down to produce body odor. ○ Sebaceous Glands: Produce sebum, an oily substance that lubricates and waterproofs the skin and hair. 4. Sensory Receptors: ○ Meissner's Corpuscles: Detect light touch and are abundant in hairless skin like fingertips. ○ Pacinian Corpuscles: Detect deep pressure and vibration. ○ Merkel Cells: Detect fine touch and texture, found in the stratum basale. 4. Skin Color, Skin Texture, and the Effects of Aging on the Skin 1. Skin Color: ○ Determined by the amount and type of melanin produced by melanocytes in the stratum basale. ○ Melanin: Provides pigmentation and protects against UV radiation. Variations in melanin types (eumelanin and pheomelanin) result in different skin tones. ○ Carotene: Yellow-orange pigment found in the stratum corneum and adipose tissue. ○ Hemoglobin: Red pigment in blood that affects skin color, especially in lighter-skinned individuals. 2. Skin Texture: ○ Determined by the organization and density of collagen and elastin fibers in the dermis, as well as the hydration and condition of the stratum corneum. 3. Effects of Aging: ○ Epidermal Thinning: The epidermis becomes thinner, leading to increased fragility and decreased barrier function. ○ Decreased Collagen and Elastin: Reduction in collagen and elastin fibers causes wrinkling and loss of skin elasticity. ○ Reduced Sebum Production: Leads to drier skin and increased susceptibility to irritation and infections. 5. Dermatological Features 1. Freckles (Ephelides): Small, flat, pigmented spots caused by increased melanin production. More common in fair-skinned individuals and become more prominent with sun exposure. 2. Moles (Nevi): Benign growths of melanocytes. Can be congenital or acquired and vary in color, size, and shape. Dysplastic nevi have irregular borders and may indicate a risk of melanoma. 3. Scales: Flakes of keratinized skin, often associated with conditions like psoriasis or eczema. 4. Calluses: Thickened skin due to repeated friction or pressure, often found on hands and feet. 5. Birthmarks: Pigmented or vascular skin anomalies present at birth, such as hemangiomas or café-au-lait spots. 6. Fingerprints: Unique patterns formed by dermal ridges on the fingertips. They increase friction and enhance grip. 6. Diseases Affecting the Skin 1. Wounds Affecting the Skin: ○ Burns: First-degree Burns: Affect only the epidermis. Symptoms include redness, pain, and minor swelling. Healing occurs within a few days without scarring. Second-degree Burns: Extend into the dermis. Characterized by blisters, intense pain, and swelling. Healing may take weeks, and scarring is possible. Third-degree Burns: Penetrate through the entire dermis and affect underlying tissues. The skin may appear charred, white, or leathery, and the area may be numb due to nerve damage. Requires immediate medical attention and often surgical intervention, such as skin grafting. ○ Sunburn: Caused by excessive UV radiation leading to DNA damage in skin cells. Symptoms include redness, pain, swelling, and peeling. Severe sunburn can lead to blistering and increased risk of skin cancer. 2. Allergens: ○ Poison Ivy: An allergic reaction to urushiol, an oil found in the plant. Symptoms include itchy, red, blistering rash. Treated with topical steroids and antihistamines. ○ Metals (Nickel Allergy): Contact dermatitis resulting from an immune response to metal ions. Symptoms include redness, itching, and blisters. Avoidance of the allergen and use of topical corticosteroids are common treatments. 3. Human Papillomavirus (HPV): ○ Causes warts, which are benign growths on the skin or mucous membranes. Common types include: Common Warts (Verruca Vulgaris): Typically found on hands and fingers. Plantar Warts: Occur on the soles of the feet and can be painful. Flat Warts: Small, smooth warts that appear in clusters, usually on the face or legs. ○ Treatments include cryotherapy, salicylic acid, and laser therapy. 4. Infections: ○ Boils (Furuncles) and Carbuncles: Infections of hair follicles by Staphylococcus aureus. Boils are localized, while carbuncles involve multiple follicles. Treated with drainage and antibiotics. ○ Athlete’s Foot (Tinea Pedis): Fungal infection causing itching, redness, and scaling between toes. Treated with antifungal medications. ○ Impetigo: Superficial bacterial infection, usually caused by Staphylococcus or Streptococcus. Characterized by honey-colored crusts. Treated with topical or oral antibiotics. ○ Erysipelas: Acute bacterial infection affecting the upper dermis, typically caused by Streptococcus pyogenes. Symptoms include red, raised, and well-demarcated rash. Treated with antibiotics. ○ Cellulitis: Bacterial infection of the dermis and subcutaneous tissue. Symptoms include redness, swelling, and pain. Requires prompt antibiotic treatment. ○ Hansen’s Disease (Leprosy): Caused by Mycobacterium leprae. It affects the skin, nerves, and mucous membranes. Symptoms include hypopigmented patches, sensory loss, and disfigurement. Treated with multi-drug therapy. ○ Chickenpox and Shingles: Caused by the varicella-zoster virus. Chickenpox is a primary infection, while shingles (herpes zoster) is a reactivation in adulthood, causing painful, blistering rash along nerve pathways. Antiviral medications and pain management are used for treatment. 5. Common Inflammatory Disorders: ○ Psoriasis: An autoimmune condition characterized by rapid keratinocyte proliferation, leading to red, scaly plaques. Commonly affects elbows, knees, and scalp. Treated with topical corticosteroids, vitamin D analogs, phototherapy, and systemic medications. ○ Dermatitis: Inflammation of the skin, including: Atopic Dermatitis (Eczema): Chronic, relapsing inflammatory condition associated with a defective skin barrier. Symptoms include itching, redness, and scaling. Managed with emollients, topical corticosteroids, and immunomodulators. Contact Dermatitis: Inflammatory reaction to irritants or allergens. Managed by avoiding triggers and using topical steroids. 6. Skin Cancer: ○ Melanoma: Malignant tumor of melanocytes. Often appears as a dark, irregular mole that changes in size, shape, or color. High risk of metastasis. Treated with surgical excision, immunotherapy, and targeted therapy. ○ Basal Cell Carcinoma (BCC): The most common skin cancer, arising from the basal cells. It appears as a pearly nodule with central ulceration and telangiectasia. Rarely metastasizes but can be locally invasive. Treated with surgical excision, cryotherapy, or topical medications. ○ Squamous Cell Carcinoma (SCC): Arises from keratinocytes in the epidermis. It presents as a scaly, red patch or ulcer. It can metastasize if untreated. Treated with surgical excision, radiation therapy, and topical agents. ○ Kaposi’s Sarcoma: A cancer arising from endothelial cells, associated with human herpesvirus 8 (HHV-8) and often seen in immunocompromised individuals (e.g., HIV/AIDS patients). Presents as purple lesions on the skin and mucous membranes. Treated with antiretroviral therapy, chemotherapy, and radiation. ○ Merkel Cell Carcinoma: A rare and aggressive neuroendocrine tumor of the skin. It appears as a painless, fast-growing nodule. Treated with surgery, radiation, and immunotherapy. 7. Treatments and Prevention 1. Wounds and Burns: ○ First-degree Burns: Cool water, aloe vera, and over-the-counter pain relievers. ○ Second-degree Burns: Moist dressings, pain management, and topical antibiotics if blistered. ○ Third-degree Burns: Requires immediate medical attention, fluid resuscitation, and possibly surgical debridement or skin grafting. 2. Allergens and Irritations: ○ Avoidance of known allergens, use of topical corticosteroids, and antihistamines. 3. HPV and Warts: ○ Treatments include cryotherapy, salicylic acid, laser therapy, and immunomodulating agents. 4. Bacterial and Fungal Infections: ○ Antibiotics for bacterial infections (e.g., cellulitis, impetigo). ○ Antifungal agents for fungal infections (e.g., athlete’s foot). 5. Psoriasis and Dermatitis: ○ Topical Treatments: Corticosteroids, vitamin D analogs, calcineurin inhibitors. ○ Systemic Treatments: Methotrexate, cyclosporine, biologics. ○ Phototherapy: UVB therapy for widespread psoriasis or eczema. 6. Skin Cancer: ○ Surgical Excision: The primary treatment for most skin cancers. ○ Radiation Therapy: For inoperable tumors or metastatic disease. ○ Chemotherapy and Immunotherapy: Used in advanced melanoma and Merkel cell carcinoma. 1. Cellular Components of the Cutaneous Immune System The skin is not just a physical barrier but also an active immune organ with several specialized cells that contribute to both innate and adaptive immunity. The following are the primary cellular components involved in the cutaneous immune response: A. Dermal Dendritic Cells (DCs) Location: Found in the dermis and epidermis. Function: ○ Act as antigen-presenting cells (APCs). ○ Capture antigens from pathogens or damaged cells and present them to T cells in lymph nodes. ○ Initiate the adaptive immune response by interacting with naïve T cells. Subtypes: ○ Langerhans Cells: A specific type of dendritic cell located primarily in the epidermis. They contain Birbeck granules and play a crucial role in detecting and presenting antigens. ○ Dermal Dendritic Cells: Found in the dermis, they are involved in capturing antigens and migrating to lymph nodes for T-cell activation. B. Dermal Macrophages Location: Distributed throughout the dermis. Function: ○ Phagocytose pathogens, dead cells, and debris. ○ Act as APCs, similar to dendritic cells, by presenting antigens to T cells. ○ Release cytokines and chemokines that modulate the immune response. ○ Contribute to tissue repair and remodeling by secreting growth factors. C. Keratinocytes Location: Predominantly in the epidermis. Function: ○ Produce antimicrobial peptides like defensins and cathelicidins. ○ Secrete cytokines (e.g., IL-1, TNF-α) that initiate and regulate immune responses. ○ Serve as a physical barrier to infection. D. Mast Cells Location: Found in the dermis near blood vessels. Function: ○ Release histamine and other mediators during allergic reactions. ○ Play a role in the defense against parasitic infections. ○ Involved in wound healing and angiogenesis. E. T Cells Location: Present in both the dermis and epidermis. Function: ○ CD8+ Cytotoxic T Cells: Kill infected or malignant cells. ○ CD4+ Helper T Cells: Modulate the immune response by secreting cytokines. ○ Regulatory T Cells: Maintain immune tolerance and prevent autoimmunity. F. B Cells and Plasma Cells Location: Rare in normal skin but can be present in inflammatory conditions. Function: ○ Produce antibodies against pathogens. ○ Participate in autoimmune responses. 2. Additional Immunologic and Inflammatory Disorders A. Rosacea Pathophysiology: Chronic inflammatory skin condition affecting the central face. Characterized by flushing, erythema, papules, pustules, and telangiectasia. Triggers: Sun exposure, heat, spicy foods, alcohol, stress. Subtypes: ○ Erythematotelangiectatic: Persistent redness and visible blood vessels. ○ Papulopustular: Redness with acne-like breakouts. ○ Phymatous: Skin thickening, especially around the nose (rhinophyma). ○ Ocular: Affects eyes, causing redness, irritation, and dryness. Treatment: ○ Topical: Metronidazole, azelaic acid, ivermectin. ○ Oral: Doxycycline, isotretinoin for severe cases. ○ Laser Therapy: For reducing visible blood vessels and redness. ○ Prevention: Avoid triggers, use sunscreen, gentle skincare. B. Vitiligo Pathophysiology: Autoimmune destruction of melanocytes leading to depigmented patches of skin. Types: ○ Generalized: Symmetric, widespread patches. ○ Segmental: Unilateral, affecting only one part of the body. ○ Focal: Small, localized area. Associated Conditions: Thyroid disease, alopecia areata, diabetes mellitus. Treatment: ○ Topical Corticosteroids: For small areas. ○ Topical Calcineurin Inhibitors: Tacrolimus and pimecrolimus. ○ Phototherapy: Narrowband UVB or PUVA therapy. ○ Depigmentation Therapy: Monobenzone for extensive vitiligo. ○ Surgical Options: Skin grafts or melanocyte transplantation for stable vitiligo. C. Bullous Pemphigoid Pathophysiology: Autoimmune disorder characterized by antibodies against hemidesmosomes, leading to subepidermal blistering. Symptoms: Tense, fluid-filled blisters on erythematous skin, usually on the trunk and limbs. Diagnosis: ○ Direct Immunofluorescence: Linear deposition of IgG and C3 along the basement membrane. ○ ELISA: Detects circulating anti-BP180 and anti-BP230 antibodies. Treatment: ○ Topical Corticosteroids: High-potency for localized disease. ○ Systemic Corticosteroids: Prednisone for widespread involvement. ○ Immunosuppressants: Azathioprine, mycophenolate mofetil. ○ Biologics: Rituximab for refractory cases. D. Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) Pathophysiology: Severe, life-threatening reactions often triggered by medications (e.g., antibiotics, anticonvulsants) or infections. SJS involves 30% BSA. Symptoms: Painful, erythematous macules, blisters, and mucosal involvement. Skin sloughs off, resembling severe burns. Diagnosis: Clinical presentation, history of drug exposure, and skin biopsy showing epidermal necrosis. Treatment: ○ Discontinuation of Offending Agent: Immediate cessation of the causative drug. ○ Supportive Care: Hospitalization, fluid and electrolyte management, wound care similar to burn treatment. ○ Medications: Intravenous immunoglobulin (IVIG), corticosteroids, and cyclosporine in some cases. ○ Prevention: Genetic testing (e.g., HLA-B*1502 for carbamazepine in Asian populations) to identify susceptibility. E. Erythema Nodosum Pathophysiology: Inflammatory condition affecting the subcutaneous fat, often triggered by infections, medications, or systemic diseases like sarcoidosis. Symptoms: Painful, red nodules typically located on the shins. Diagnosis: Clinical presentation and, if needed, biopsy showing panniculitis. Treatment: ○ Treat Underlying Cause: Identify and treat infections or discontinue causative medications. ○ NSAIDs: For pain relief and inflammation reduction. ○ Potassium Iodide: Occasionally used in chronic cases. ○ Systemic Corticosteroids: For severe or refractory cases. F. Erythema Multiforme Pathophysiology: Immune-mediated hypersensitivity reaction, often triggered by infections (e.g., HSV, Mycoplasma) or medications. Symptoms: Target lesions with concentric rings, typically on extremities. Severe cases may involve mucous membranes. Diagnosis: Clinical presentation, history of trigger, and biopsy if needed. Treatment: ○ Mild Cases: Symptomatic treatment with antihistamines, topical corticosteroids. ○ Severe Cases: Systemic corticosteroids, antiviral therapy for HSV-associated cases. ○ Prevention: Prophylactic antiviral therapy for recurrent cases linked to HSV. G. Alopecia Types: ○ Alopecia Areata: Autoimmune condition leading to patchy hair loss. ○ Androgenetic Alopecia: Genetically predisposed hair loss due to sensitivity to androgens. ○ Telogen Effluvium: Diffuse hair shedding following a stressful event. Diagnosis: Clinical examination, scalp biopsy, and hormonal testing if indicated. Treatment: ○ Alopecia Areata: Intralesional corticosteroids, topical immunotherapy (e.g., diphenylcyclopropenone), JAK inhibitors (off-label). ○ Androgenetic Alopecia: Minoxidil, finasteride for men, spironolactone for women. ○ Telogen Effluvium: Treat underlying cause; hair regrowth typically occurs spontaneously. 3. Additional Congenital Disorders A. Albinism Pathophysiology: Genetic disorder characterized by a deficiency in melanin production due to defects in the enzymes involved in melanin synthesis, most commonly tyrosinase. Types: ○ Oculocutaneous Albinism (OCA): Affects the skin, hair, and eyes. ○ Ocular Albinism: Primarily affects the eyes, with minimal skin and hair involvement. Symptoms: Pale skin, white hair, and light-colored eyes. Increased risk of skin cancer and vision problems (e.g., nystagmus, photophobia). Treatment: ○ Sun Protection: Use of sunscreen, protective clothing, and sunglasses. ○ Vision Support: Corrective lenses, regular eye exams. ○ Genetic Counseling: For affected families. B. Xeroderma Pigmentosum (XP) Pathophysiology: Autosomal recessive disorder characterized by a defect in DNA repair, leading to extreme sensitivity to UV radiation and a high risk of skin cancers. Symptoms: Severe sunburn after minimal sun exposure, freckling, skin atrophy, and multiple skin cancers at an early age. Diagnosis: Clinical suspicion, genetic testing, and cellular tests for DNA repair deficiency. Treatment: ○ Strict Sun Avoidance: UV-blocking clothing, sunscreen, and protective eyewear. ○ Regular Skin Checks: For early detection of skin cancers. ○ Treatment of Cancers: Surgical excision, cryotherapy, or topical agents. C. Acanthosis Nigricans Pathophysiology: Thickened, hyperpigmented skin often found in body folds (e.g., neck, axillae). Associated with insulin resistance, obesity, or malignancy. Symptoms: Velvety, brownish plaques. May be asymptomatic or associated with pruritus. Diagnosis: Clinical presentation, blood tests for insulin resistance, and malignancy screening if indicated. Treatment: ○ Weight Loss: Improves insulin sensitivity. ○ Topical Agents: Keratolytics (e.g., salicylic acid), retinoids, or laser therapy. ○ Treatment of Underlying Condition: Management of diabetes or cancer if present. 4. Benign Lesions A. Actinic Keratosis (AK) Pathophysiology: Precancerous lesions caused by chronic sun exposure, with a risk of progression to squamous cell carcinoma. Symptoms: Rough, scaly patches or plaques on sun-exposed areas (e.g., face, ears, hands). Diagnosis: Clinical examination, dermoscopy, and biopsy if needed. Treatment: ○ Topical Agents: 5-fluorouracil, imiquimod, diclofenac gel. ○ Cryotherapy: Liquid nitrogen to freeze and destroy the lesion. ○ Photodynamic Therapy (PDT): Application of a photosensitizing agent followed by light exposure. ○ Prevention: Sun protection and regular skin exams. 5. Aspects of Wound Healing A. Inflammation: First Phase of Wound Healing: Involves the recruitment of inflammatory cells (neutrophils, macrophages) to the wound site. Cytokines like IL-1 and TNF-α play a key role. Vasodilation: Increased blood flow to the area, mediated by histamine, prostaglandins, and nitric oxide. Outcomes: Clearing of debris and pathogens, setting the stage for tissue repair. B. Necrosis: Definition: Cell death due to injury, resulting in the release of intracellular contents, which can induce further inflammation. Role in Wound Healing: Necrotic tissue must be cleared by phagocytes for proper healing to occur. C. Apoptosis: Definition: Programmed cell death that occurs without inducing inflammation. Role in Wound Healing: Helps remove cells that are no longer needed, such as excess inflammatory cells, to allow for tissue remodeling. D. Clotting and Vasoconstriction: Initial Response: Platelets aggregate at the wound site, releasing factors like thromboxane A2, which causes vasoconstriction. Clot Formation: Fibrinogen is converted to fibrin, forming a stable clot that acts as a scaffold for cellular migration and tissue repair. 6. Skeletal System Overview A. Bone Structure and Function: Axial Skeleton: Skull, vertebral column, ribs, and sternum. Appendicular Skeleton: Limbs, pectoral and pelvic girdles. Surface Anatomy: Features like foramina, tubercles, condyles, and grooves seen on X-rays, CT, and MRI. Bone Marrow: Red marrow (hematopoiesis) and yellow marrow (fat storage). B. Joint Types and Movement: Fibrous, Cartilaginous, and Synovial Joints: Their anatomy and ranges of motion. Ligaments and Tendons: Connect bones to bones and muscles to bones, respectively. C. Cellular Composition and Function: Osteoblasts, Osteocytes, Osteoclasts: Their roles in bone formation and resorption. Bone Marrow Cells: Hematopoietic stem cells, mesenchymal cells. D. Bone Disorders: Osteoarthritis: Degenerative joint disease. Rheumatoid Arthritis: Autoimmune condition affecting synovial joints. Gout: Uric acid crystal deposition in joints. Osteoporosis: Decreased bone density, increased fracture risk. Osteomalacia/Rickets: Defective bone mineralization due to vitamin D deficiency. Scoliosis, Kyphosis, Lordosis: Abnormal spinal curvatures. Tennis and Golfer’s Elbow: Tendinitis affecting the elbow. Cruciate Ligament and Meniscus Tears: Common knee injuries. Septic Arthritis: Joint infection requiring urgent treatment. 7. Bone and Cartilage Disorders: Treatments A. Osteoarthritis and Rheumatoid Arthritis: NSAIDs, DMARDs, Biologics, Surgery. B. Gout: Colchicine, NSAIDs, Xanthine Oxidase Inhibitors. C. Osteoporosis: Bisphosphonates, Calcium/Vitamin D, Hormone Replacement. D. Bone Healing: Immobilization, Surgical Fixation, Bone Grafts. DETAIL, IF I HAVE TIME: 1. Rosacea Pathophysiology: ○ A chronic inflammatory skin condition with an unclear etiology but involves vascular hyperreactivity, altered immune response, and Demodex mite colonization. ○ Increased presence of cathelicidins and Toll-like receptor 2 in the skin, leading to an exaggerated inflammatory response. Symptoms: ○ Flushing, persistent redness, visible blood vessels, acne-like bumps, thickened skin, and ocular symptoms like dryness or irritation. Diagnosis: ○ Clinical diagnosis based on history and symptoms. Biopsy is rarely required unless another diagnosis is suspected. Subtypes: ○ Erythematotelangiectatic: Persistent facial redness, visible blood vessels. ○ Papulopustular: Redness with pustules and papules similar to acne. ○ Phymatous: Skin thickening and irregular surface, typically around the nose. ○ Ocular: Symptoms affecting the eyes, such as conjunctivitis, blepharitis. Treatment: ○ Topical Medications: Metronidazole, azelaic acid, ivermectin. ○ Oral Medications: Doxycycline or minocycline for moderate to severe cases. ○ Laser Therapy: Pulsed dye laser or intense pulsed light (IPL) for telangiectasia and redness. ○ Lifestyle Management: Avoid triggers (e.g., heat, alcohol, spicy foods). 2. Vitiligo Pathophysiology: ○ Autoimmune destruction of melanocytes, leading to depigmented macules and patches. Genetic predisposition, oxidative stress, and neural factors may contribute. Symptoms: ○ Sharply demarcated white patches, commonly on the face, hands, and around body orifices. Symmetric distribution is typical in non-segmental vitiligo. Diagnosis: ○ Wood's lamp examination reveals areas of depigmentation. Biopsy shows the absence of melanocytes in the affected skin. Treatment: ○ Topical Corticosteroids: Clobetasol for localized disease. ○ Topical Calcineurin Inhibitors: Tacrolimus for sensitive areas like the face. ○ Phototherapy: Narrowband UVB or PUVA therapy for extensive involvement. ○ Depigmentation Therapy: Monobenzone for patients with extensive involvement (>50% BSA). ○ Surgical Options: Melanocyte transplantation or skin grafting for stable patches. ○ Cosmetic Camouflage: Makeup or tattooing to match skin tone. 3. Bullous Pemphigoid Pathophysiology: ○ Autoimmune blistering disorder with antibodies against hemidesmosomal proteins BP180 (collagen XVII) and BP230, causing separation at the dermo-epidermal junction. Symptoms: ○ Tense blisters on normal or erythematous skin, primarily on the trunk and limbs. Itching often precedes blister formation. Diagnosis: ○ Direct Immunofluorescence: IgG and C3 deposition along the basement membrane. ○ ELISA: Detection of circulating anti-BP180 and anti-BP230 antibodies. Treatment: ○ Topical Corticosteroids: High-potency steroids like clobetasol for mild cases. ○ Systemic Corticosteroids: Prednisone for extensive disease. ○ Immunosuppressive Agents: Azathioprine or mycophenolate mofetil in steroid-sparing regimens. ○ Biologics: Rituximab for refractory cases. 4. Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) Pathophysiology: ○ Severe mucocutaneous reactions, most commonly triggered by medications (e.g., sulfonamides, anticonvulsants) or infections. SJS affects 30%. Symptoms: ○ Initial flu-like symptoms, followed by painful, erythematous macules that coalesce, blister, and lead to extensive skin detachment. Involvement of mucous membranes is common. Diagnosis: ○ Clinical diagnosis supported by skin biopsy showing necrosis of the epidermis and subepidermal blister formation. Treatment: ○ Immediate Cessation of Offending Agent: This is crucial. ○ Supportive Care: Similar to burn treatment, with meticulous fluid and electrolyte management, wound care, and infection control. ○ Medications: Intravenous immunoglobulin (IVIG) may be beneficial. Corticosteroids and cyclosporine are used in some cases. ○ Prevention: Genetic screening for specific HLA alleles (e.g., HLA-B*1502 in carbamazepine use). 5. Erythema Nodosum Pathophysiology: ○ Inflammatory reaction in the subcutaneous fat (panniculitis), often associated with infections (e.g., streptococcal), medications (e.g., oral contraceptives), or systemic diseases (e.g., sarcoidosis). Symptoms: ○ Painful, red, firm nodules typically on the anterior lower legs. May be accompanied by fever, malaise, and arthralgia. Diagnosis: ○ Clinical examination, supported by elevated inflammatory markers (ESR, CRP). Biopsy shows septal panniculitis without vasculitis. Treatment: ○ Treat Underlying Cause: E.g., antibiotics for streptococcal infection. ○ NSAIDs: For pain and inflammation relief. ○ Corticosteroids: For severe cases or where an underlying condition requires management. ○ Potassium Iodide: Occasionally used in chronic cases. 6. Erythema Multiforme Pathophysiology: ○ Acute, immune-mediated condition often triggered by infections (HSV, Mycoplasma) or drugs. Characterized by targetoid lesions. Symptoms: ○ Target lesions with a central dusky zone, often on palms, soles, and extensor surfaces. Severe cases may involve oral, ocular, and genital mucosa. Diagnosis: ○ Clinical presentation and history. Skin biopsy shows interface dermatitis with necrotic keratinocytes. Treatment: ○ Mild Cases: Symptomatic relief with antihistamines, topical steroids. ○ Severe Cases: Systemic corticosteroids, antivirals for HSV-triggered cases. ○ Prevention: Prophylactic antivirals in recurrent HSV-associated cases. 7. Alopecia Types: 1. Alopecia Areata: Autoimmune condition leading to well-demarcated patches of hair loss. Linked to other autoimmune conditions like thyroid disease. Treatment: Intralesional corticosteroids, topical immunotherapy, JAK inhibitors (off-label use). 2. Androgenetic Alopecia: Genetic and hormonal influences leading to patterned hair loss in men and women. Treatment: Minoxidil, finasteride, spironolactone for women, hair transplant surgery. 3. Telogen Effluvium: Diffuse hair shedding following stress, illness, or hormonal changes. Treatment: Address underlying cause, reassurance as it is often self-limiting. 8. Albinism Pathophysiology: ○ Genetic disorders affecting melanin synthesis. Most commonly due to tyrosinase enzyme deficiency, leading to decreased melanin in the skin, hair, and eyes. Symptoms: ○ Pale skin, white hair, and light-colored irises. Vision problems like nystagmus, strabismus, and photophobia. Diagnosis: ○ Clinical examination, genetic testing for specific gene mutations. Treatment: ○ Sun Protection: Regular use of sunscreen and protective clothing to prevent skin cancer. ○ Vision Support: Prescription glasses, visual aids. ○ Genetic Counseling: Advising families on inheritance patterns and risks. 9. Xeroderma Pigmentosum (XP) Pathophysiology: ○ Autosomal recessive disorder caused by defects in DNA repair enzymes, leading to an inability to repair UV-induced DNA damage. Symptoms: ○ Severe sun sensitivity, freckling, early-onset skin cancer, neurological abnormalities in some cases. Diagnosis: ○ Clinical signs, genetic testing, cellular assays for UV sensitivity. Treatment: ○ Strict UV Protection: Use of high-SPF sunscreens, protective clothing, UV-blocking windows. ○ Regular Dermatological Exams: For early detection of skin malignancies. ○ Therapeutic Interventions: Surgery, cryotherapy, or topical agents for skin cancers. 10. Acanthosis Nigricans Pathophysiology: ○ Thickening and hyperpigmentation of the skin, commonly associated with insulin resistance, obesity, and rarely, malignancy. Symptoms: ○ Velvety, dark patches in skin folds like the neck, axillae, and groin. Diagnosis: ○ Clinical diagnosis, assessing for underlying conditions like diabetes. Treatment: ○ Weight Loss: Improves insulin sensitivity and reduces skin changes. ○ Topical Treatments: Keratolytics, retinoids, laser therapy for cosmetic purposes. ○ Management of Underlying Conditions: Control of diabetes, malignancy treatment The Effects of Exercise and Aging on the Skeletal System Exercise: Bone Density and Strength: ○ Weight-bearing and resistance exercises, like walking, running, and lifting weights, stimulate osteoblast activity, increasing bone mineral density (BMD) and overall bone strength. This adaptation is due to the mechanical load creating microstrain in the bone, activating the mechanotransduction pathway. ○ Exercises promote the release of growth factors like Insulin-like Growth Factor 1 (IGF-1) and Bone Morphogenetic Proteins (BMPs), which are crucial for bone remodeling. Bone Remodeling: ○ The process of bone remodeling is regulated by the balance between osteoclast-mediated bone resorption and osteoblast-mediated bone formation. Regular physical activity shifts this balance towards bone formation, reducing the risk of osteoporosis and fractures. Joint Health: ○ Exercise increases the production of synovial fluid, which lubricates joints and delivers nutrients to the cartilage, enhancing joint flexibility and reducing the risk of degenerative joint diseases like osteoarthritis. Aging: Bone Loss: ○ With aging, there is a decline in bone remodeling activity, with osteoclast activity outpacing osteoblast activity, leading to reduced bone density (osteopenia) and increased risk of osteoporosis. This is particularly pronounced in postmenopausal women due to decreased estrogen levels, a hormone that inhibits osteoclast activity. Changes in Bone Microarchitecture: ○ The trabecular bone, which provides structural support, becomes thinner and more porous, leading to increased bone fragility. The cortical bone also becomes thinner, contributing to a higher risk of fractures. Joint Degeneration: ○ Aging leads to the thinning of articular cartilage and reduced synovial fluid production, which can cause joint stiffness and pain. This contributes to the development of osteoarthritis. Fractures and the Salter-Harris Classification System Types of Fractures: Simple Fractures: The bone breaks cleanly but does not penetrate the skin. Compound (Open) Fractures: The bone pierces the skin, increasing the risk of infection. Comminuted Fractures: The bone shatters into multiple fragments. Greenstick Fractures: Incomplete fractures commonly seen in children where one side of the bone bends. Spiral Fractures: Caused by a twisting force, often seen in sports injuries. Stress Fractures: Small cracks in the bone resulting from repetitive force or overuse, common in athletes. Salter-Harris Fracture Classification: This system classifies fractures involving the growth plate (physis) in children: Type I: Fracture through the growth plate without bone involvement. Prognosis is excellent. Type II: Fracture through the growth plate and metaphysis (the long part of the bone), sparing the epiphysis. Most common type, good prognosis. Type III: Fracture through the growth plate and epiphysis, affecting the joint surface. Requires precise realignment. Type IV: Fracture through the growth plate, metaphysis, and epiphysis. May cause growth disturbances if not properly treated. Type V: Crush injury to the growth plate. Rare and often associated with growth arrest. Causes and Treatments: Causes: Trauma, overuse, osteoporosis, or pathological conditions like tumors. Treatments: ○ Non-Surgical: Immobilization with casts or splints for stable fractures. ○ Surgical: Internal fixation using plates, screws, or rods for unstable fractures. ○ Rehabilitation: Physical therapy to restore strength and mobility post-fracture. Additional Skeletal Disorders Spinal Fractures: Compression Fractures: Typically caused by osteoporosis. The vertebral body collapses, leading to a wedge shape. Burst Fractures: Result from high-energy trauma. The vertebra breaks into several pieces, which can impinge on the spinal cord. Chance Fractures: Result from flexion-distraction injuries, often due to seatbelt trauma in car accidents. They involve all three columns of the spine. Ankylosing Spondylitis: Pathophysiology: Chronic inflammatory disease primarily affecting the spine and sacroiliac joints, leading to eventual fusion (ankylosis). Associated with the HLA-B27 genetic marker. Symptoms: Lower back pain, morning stiffness, and reduced flexibility. Advanced cases show "bamboo spine" on X-rays due to vertebral fusion. Treatment: NSAIDs, biologics like TNF inhibitors (e.g., infliximab), and physical therapy. Achondroplasia: Pathophysiology: A genetic disorder caused by mutations in the FGFR3 gene, leading to abnormal cartilage formation and short stature. Symptoms: Short limbs, normal trunk length, large head with frontal bossing, and midface hypoplasia. Treatment: There is no cure; management focuses on treating complications like spinal stenosis or hydrocephalus. Osteosarcoma and Ewing Sarcoma: Osteosarcoma: ○ Pathophysiology: A malignant tumor of osteoblasts, commonly affecting the metaphysis of long bones. Most frequent in adolescents and young adults. ○ Symptoms: Pain, swelling, and a palpable mass, often near the knee. ○ Treatment: Chemotherapy followed by surgical resection. Limb-salvage surgery or amputation may be required. Ewing Sarcoma: ○ Pathophysiology: A malignant tumor arising from the bone or soft tissue, associated with the EWS-FLI1 fusion gene. Common in adolescents and young adults. ○ Symptoms: Pain, swelling, fever, and an elevated white blood cell count. ○ Treatment: Chemotherapy, radiation, and surgical resection. Multimodal therapy improves survival rates. Effects of Bisphosphonates and Denosumab on the Skeletal System Bisphosphonates (e.g., Alendronate, Zoledronic Acid): ○ Mechanism: Inhibit osteoclast-mediated bone resorption by binding to hydroxyapatite in bone, reducing bone turnover. ○ Uses: Treatment of osteoporosis, Paget’s disease, and hypercalcemia of malignancy. ○ Side Effects: Gastrointestinal issues, osteonecrosis of the jaw, atypical femoral fractures. Denosumab: ○ Mechanism: A monoclonal antibody that inhibits RANKL, preventing osteoclast formation and function, thus reducing bone resorption. ○ Uses: Osteoporosis, bone metastases, and giant cell tumor of bone. ○ Side Effects: Hypocalcemia, risk of infections, and osteonecrosis of the jaw. Additional Skeletal Disorders Spinal Stenosis and Foraminal Stenosis: Pathophysiology: Narrowing of the spinal canal or intervertebral foramina, causing compression of the spinal cord or nerve roots. Symptoms: Back pain, neurogenic claudication, weakness, and paresthesia. Treatment: NSAIDs, physical therapy, epidural steroid injections, and surgical decompression in severe cases. Disc Herniation: Pathophysiology: The nucleus pulposus protrudes through a tear in the annulus fibrosus, compressing nearby nerves. Symptoms: Radicular pain, numbness, and weakness corresponding to the affected nerve root. Treatment: Conservative management with rest, NSAIDs, physical therapy. Surgery (discectomy) if there is neurological deficit or intractable pain. Osgood-Schlatter Disease: Pathophysiology: Inflammation of the tibial tuberosity due to repetitive stress from the quadriceps muscle, commonly seen in adolescents during growth spurts. Symptoms: Pain and swelling below the kneecap, especially during activities like running or jumping. Treatment: Rest, ice, NSAIDs, and physical therapy to strengthen the quadriceps. Plantar Fasciitis: Pathophysiology: Inflammation of the plantar fascia, often due to overuse, poor footwear, or biomechanical issues. Symptoms: Heel pain, particularly in the morning or after prolonged rest. Treatment: Rest, ice, stretching exercises, orthotics, NSAIDs, and in severe cases, corticosteroid injections or surgery. Paget’s Disease of Bone (Osteitis Deformans): Pathophysiology: Disorganized bone remodeling leads to structurally abnormal, enlarged, and weakened bones. Caused by increased osteoclast activity. Symptoms: Bone pain, deformities, fractures, and in severe cases, hearing loss due to skull involvement. Treatment: Bisphosphonates to inhibit bone resorption, calcitonin, and surgical intervention for complications like fractures or severe deformities. Osteoblastoma: Pathophysiology: A benign, but aggressive bone tumor that commonly affects the spine and long bones in young adults. Symptoms: Pain, often not relieved by NSAIDs, and possible neurological symptoms if the spine is involved. Treatment: Surgical excision or curettage. Radiation therapy for lesions not amenable to surgery. Giant Cell Tumor of Bone: Pathophysiology: 1. Giant Cell Tumor (GCT) Giant Cell Tumor (GCT) of bone is a benign but locally aggressive tumor characterized by the presence of multinucleated giant cells (osteoclast-like cells). These tumors typically arise in the epiphyses of long bones, especially in the distal femur, proximal tibia, and distal radius. Although benign, they can cause significant bone destruction and sometimes extend into soft tissues. Pathophysiology: GCT consists of a mixture of mononuclear stromal cells, multinucleated giant cells, and reactive bone formation. The stromal cells are thought to be the neoplastic component, while the giant cells are reactive and resemble osteoclasts. GCTs are typically classified as benign but can occasionally undergo malignant transformation or metastasize, particularly to the lungs. Treatment Options: Surgical resection: The mainstay of treatment for GCT. This can involve intralesional curettage (scraping out the tumor), followed by bone grafting or cementing to fill the defect. In cases of more extensive involvement, en bloc resection may be needed. Denosumab: A monoclonal antibody targeting RANKL, a key regulator of osteoclast differentiation and activity, is often used as a neoadjuvant treatment to reduce the size of the tumor before surgery. Radiation therapy: Considered in cases where surgery is not possible or the tumor recurs. 2. Treatments and/or Prevention for All Conditions Listed Above (Drugs, Surgery, etc.) Treatments vary widely depending on the specific condition: Myasthenia Gravis: ○ Drugs: Anticholinesterase agents (e.g., pyridostigmine), immunosuppressants (e.g., prednisone, azathioprine), and monoclonal antibodies (e.g., rituximab). ○ Surgery: Thymectomy is often performed if thymoma is present or in generalized MG. Lambert-Eaton Myasthenic Syndrome: ○ Drugs: Pyridostigmine, aminopyridines (like 3,4-diaminopyridine), and immunosuppressants. ○ Treatment of the underlying malignancy if associated with small cell lung cancer. Polymyalgia Rheumatica: ○ Corticosteroids are the primary treatment, with doses tapered slowly over time. Polymyositis and Dermatomyositis: ○ Immunosuppressive drugs (e.g., methotrexate, azathioprine, corticosteroids) and physical therapy. Botulism: ○ Antitoxin administration and supportive care. Tetanus: ○ Antitoxin (tetanus immune globulin), muscle relaxants, wound debridement, and antibiotics. Fibromyalgia: ○ Antidepressants (e.g., duloxetine, amitriptyline), anticonvulsants (e.g., pregabalin), and physical therapy. 3. Bones and Sutures of the Skull The skull consists of 22 bones, divided into cranial bones and facial bones: Cranial Bones: Include the frontal bone, parietal bones, temporal bones, occipital bone, sphenoid bone, and ethmoid bone. Facial Bones: Include the mandible, maxillae, zygomatic bones, nasal bones, lacrimal bones, vomer, palatine bones, and inferior nasal conchae. Sutures of the Skull: Coronal Suture: Between the frontal and parietal bones. Sagittal Suture: Between the two parietal bones. Lambdoid Suture: Between the parietal bones and the occipital bone. Squamous Suture: Between the parietal and temporal bones. 4. Foramina of the Skull Foramina are openings in the skull that allow passage of neurovascular structures: Foramen Magnum: Passage for the spinal cord, vertebral arteries, and the accessory nerve (CN XI). Jugular Foramen: Passage for the glossopharyngeal (CN IX), vagus (CN X), and accessory nerves (CN XI), as well as the jugular vein. Optic Canal: Passage for the optic nerve (CN II) and ophthalmic artery. Superior Orbital Fissure: Passage for the oculomotor (CN III), trochlear (CN IV), abducens (CN VI), and ophthalmic branch of the trigeminal nerve (CN V1). Foramen Ovale: Passage for the mandibular branch of the trigeminal nerve (CN V3). 5. Muscular System i. Functions of the Muscular System: Movement: Skeletal muscles contract to create movement at joints. Blood Circulation: Cardiac muscle pumps blood throughout the body. Heat Production: Muscle contraction generates heat, helping maintain body temperature. ii. Skeletal and Muscular Systems Interaction: The skeletal and muscular systems work together to facilitate movement and maintain posture through the attachment of muscles to bones via tendons. Muscle contraction pulls on bones to produce movement, while muscles also stabilize joints to maintain posture. iii. Cellular and Gross Anatomy of Muscle Types: Skeletal Muscle: Composed of long, cylindrical, multinucleated fibers with striations. It is voluntary and controlled by the somatic nervous system. Cardiac Muscle: Short, branched, striated cells with a single nucleus. It is involuntary and controlled by the autonomic nervous system. Intercalated discs allow synchronized contractions. Smooth Muscle: Spindle-shaped, non-striated cells with a single nucleus. Found in walls of organs (e.g., digestive tract, blood vessels), and it is involuntary. iv. Tension Production in Muscle: Length-Tension Relationship: Muscle tension is affected by the length of the sarcomere before contraction. Optimal overlap of actin and myosin filaments produces maximum tension. Muscle Twitch: A single cycle of contraction and relaxation in response to a stimulus. Motor Units: A motor neuron and the muscle fibers it innervates. More motor units recruited produce greater force. v. Physiology of Skeletal Muscle Contraction and Relaxation: 1. Neuromuscular Junction: Acetylcholine (ACh) is released from the motor neuron and binds to receptors on the muscle fiber membrane, initiating an action potential. 2. Excitation-Contraction Coupling: The action potential travels along the sarcolemma and down the T-tubules, triggering calcium release from the sarcoplasmic reticulum. 3. Cross-Bridge Cycling: Calcium binds to troponin, exposing binding sites on actin. Myosin heads bind to actin, undergo a power stroke, and detach upon ATP binding. 4. Relaxation: Calcium is pumped back into the sarcoplasmic reticulum, and the muscle relaxes as cross-bridge formation ceases. vi. Skeletal Muscle Actions: Agonist: Primary muscle responsible for movement. Antagonist: Muscle that opposes the agonist. Synergist: Muscle that assists the agonist in performing its action. vii. Muscles on the 2025 National Major Skeletal Muscles List: These include key muscles involved in major movements, such as the biceps brachii, triceps brachii, quadriceps femoris, hamstrings, and deltoids. Each muscle has an origin (attachment to stationary bone), insertion (attachment to moving bone), and function (the movement it produces). viii. Exercise and Aging Effects on Muscle: Exercise: Increases muscle fiber size (hypertrophy), improves endurance, and enhances capillary density. Aging: Causes muscle atrophy (sarcopenia), reduced flexibility, and decreased strength due to loss of muscle fibers and reduced protein synthesis. ix. Muscle and Tendon Injuries: Strains: Injury to muscle fibers due to overstretching or tearing. Sprains: Injury to ligaments, often at joints, due to overextension. x. Neuromuscular Junction Disorders: Myasthenia Gravis: Autoimmune disorder that targets acetylcholine receptors, causing muscle weakness. Lambert-Eaton Myasthenic Syndrome: Autoimmune disorder that targets voltage-gated calcium channels, impairing acetylcholine release. xi. Energy Metabolism in Skeletal Muscles Skeletal muscle contraction relies on various energy sources, depending on the duration and intensity of the activity. These include: 1. Phosphocreatine System: ○ For quick, short bursts of energy, skeletal muscles use the phosphocreatine (PCr) system. Phosphocreatine donates a phosphate group to ADP, rapidly forming ATP. This system can sustain energy for approximately 10-15 seconds of intense activity, such as sprinting or lifting weights. 2. Glycogen Storage and Consumption: ○ Muscles store glucose in the form of glycogen, which can be broken down through glycogenolysis during prolonged exercise. Glucose can be metabolized anaerobically through glycolysis (producing ATP quickly but with lactic acid as a byproduct) or aerobically (producing more ATP but at a slower rate). ○ In anaerobic conditions, like intense exercise, the byproduct of glycolysis is lactate, which can lead to muscle fatigue. Aerobic metabolism, using oxygen to fully break down glucose and fat, is much more efficient for endurance activities. xii. Cardiac and Smooth Muscle Roles in the Body 1. Cardiac Muscle: ○ Blood Circulation: The primary role of cardiac muscle is to pump blood throughout the body. It is found exclusively in the walls of the heart. The rhythmic contractions of cardiac muscle, regulated by the sinoatrial (SA) node (the heart's pacemaker), maintain consistent blood flow to meet the body’s metabolic demands. ○ Structure: Cardiac muscle fibers are striated like skeletal muscle but are branched and connected by intercalated discs, which allow for synchronized contraction through gap junctions and desmosomes. This allows the heart to function as a single unit. 2. Smooth Muscle: ○ Digestive Motility: Smooth muscle is found in the walls of hollow organs (such as the stomach, intestines, bladder, and blood vessels). In the digestive system, it facilitates peristalsis, a wave-like contraction that pushes food through the gastrointestinal tract. ○ Blood Vessel Regulation: In blood vessels, smooth muscle controls vasoconstriction and vasodilation, regulating blood pressure and flow. xiii. Additional Diseases 1. Rhabdomyolysis: ○ A serious condition in which damaged muscle tissue breaks down and releases myoglobin into the bloodstream. This can lead to kidney damage and potentially fatal complications. It is often caused by extreme exercise, trauma, drug use, or infection. ○ Treatment: Early and aggressive hydration to flush out the myoglobin from the kidneys, dialysis in severe cases, and addressing the underlying cause. 2. Duchenne Muscular Dystrophy (DMD): ○ A genetic disorder caused by mutations in the dystrophin gene, leading to progressive muscle weakness and degeneration. It primarily affects boys and is usually diagnosed in early childhood. ○ Treatment: There is no cure, but treatments such as corticosteroids (e.g., prednisone) can slow progression, and physical therapy can help maintain muscle function. Gene therapies and exon-skipping drugs (e.g., eteplirsen) are emerging therapies. 3. Myotonic Dystrophy: ○ A genetic disorder characterized by muscle weakness and prolonged muscle contractions (myotonia). It can affect multiple systems, including the heart and eyes, leading to complications like arrhythmias and cataracts. ○ Treatment: Symptomatic treatments include medications like mexiletine for myotonia and devices like pacemakers for heart issues. xiv. Nerve Innervation for All Muscles on the 2025 National Major Skeletal Muscles List Muscle innervation refers to the specific motor neurons that control a muscle’s contraction. Every muscle on the National Major Skeletal Muscles List has a defined nerve supply. For example: Biceps Brachii: Innervated by the musculocutaneous nerve (C5-C7). Quadriceps Femoris: Innervated by the femoral nerve (L2-L4). Deltoid: Innervated by the axillary nerve (C5-C6). Understanding nerve innervation is crucial for diagnosing and treating neuromuscular diseases, injuries, and conditions like nerve entrapments. xv. Muscle Reflexes 1. Golgi Tendon Organ (GTO): ○ A sensory receptor located at the junction of muscle and tendon. It monitors tension in the muscle. When tension becomes too high, the GTO activates an inhibitory reflex to relax the muscle, protecting it from damage (called the Golgi tendon reflex). 2. Muscle Spindle Fibers: ○ These are stretch receptors located within muscle fibers that monitor changes in muscle length and trigger the stretch reflex. When a muscle is stretched too quickly, the spindle fibers send signals to the spinal cord, which reflexively causes the muscle to contract, preventing overstretching and injury. xvi. Additional Diseases: Congenital and Iatrogenic Disorders 1. Congenital Disorders: ○ Conditions present at birth that affect muscle function. Examples include congenital myopathies (e.g., nemaline myopathy), which are genetic disorders that lead to muscle weakness and developmental delays. 2. Iatrogenic Disorders (Drug-Induced Myositis, Malignant Hyperthermia): ○ Drug-Induced Myositis: Certain medications, such as statins or corticosteroids, can cause muscle inflammation (myositis) leading to muscle weakness and pain. Treatment includes discontinuation of the offending drug and supportive care. ○ Malignant Hyperthermia: A potentially life-threatening condition triggered by certain anesthetics (e.g., halothane) in genetically susceptible individuals. It causes a rapid increase in body temperature, muscle rigidity, and a hypermetabolic state. ○ Treatment: Immediate administration of dantrolene, which inhibits calcium release from the sarcoplasmic reticulum, and cooling the patient. xvii. Treatments and/or Prevention for All Conditions Listed Above Drugs: Treatments range from corticosteroids (for inflammatory muscle diseases) to acetylcholinesterase inhibitors (for myasthenia gravis) and monoclonal antibodies (for autoimmune conditions like Lambert-Eaton Myasthenic Syndrome). Surgery: Includes thymectomy (for myasthenia gravis), and physical therapies to improve strength and function in muscular dystrophies. Prevention: Strategies like lifestyle modifications, muscle-strengthening exercises, and early treatment can help mitigate some conditions, while genetic counseling may be relevant for congenital diseases. xviii. Effects of Steroid Medications on Muscle Health Corticosteroids (such as prednisone) are commonly used to treat inflammatory muscle diseases but can have adverse effects on muscle health over time: Muscle Atrophy: Prolonged use of corticosteroids can lead to muscle wasting due to catabolic effects on muscle protein synthesis. Steroid Myopathy: A specific condition of muscle weakness caused by chronic steroid use. Prevention and Management: Minimizing steroid use, using the lowest effective dose, and incorporating physical therapy and strength training can help mitigate these effects. Muscular System – Detailed Expansion v. Physiology of Skeletal Muscle Contraction and Relaxation Muscle contraction is a complex, multi-step process involving electrical signals, chemical interactions, and physical changes at the molecular level. This process can be divided into several stages: 1. Neuromuscular Junction (NMJ) Activation: ○ The NMJ is the synapse where a motor neuron communicates with a skeletal muscle fiber. The motor neuron releases acetylcholine (ACh), a neurotransmitter, into the synaptic cleft. ○ ACh binds to receptors on the sarcolemma (the muscle cell membrane), causing sodium ions (Na+) to rush into the muscle cell. This influx of Na+ generates an action potential, which spreads along the sarcolemma and into the T-tubules. 2. Excitation-Contraction Coupling: ○ The action potential travels down the T-tubules, triggering the sarcoplasmic reticulum (SR) to release stored calcium ions (Ca²⁺) into the cytoplasm of the muscle fiber. ○ Calcium binds to troponin, a regulatory protein attached to tropomyosin, which normally blocks the active sites on actin (a major contractile protein). When calcium binds to troponin, it causes a conformational change that shifts tropomyosin away, exposing the actin-binding sites. 3. Cross-Bridge Cycling: ○ Myosin heads, part of the thick filaments, bind to the exposed active sites on actin, forming a cross-bridge. This triggers the power stroke: the myosin heads pivot, pulling the actin filaments toward the center of the sarcomere, shortening the muscle fiber. ○ After the power stroke, ATP binds to the myosin head, causing it to release from actin. ATP is then hydrolyzed (broken down into ADP and phosphate), providing the energy to "re-cock" the myosin head for the next cycle. ○ This process repeats in a cyclical manner, as long as calcium and ATP are available. 4. Relaxation: ○ When the motor neuron stops firing, the NMJ stops releasing ACh, and acetylcholinesterase breaks down any remaining ACh in the synapse. This halts the action potential. ○ Calcium ions are actively pumped back into the sarcoplasmic reticulum via Ca²⁺-ATPase pumps, lowering the cytoplasmic calcium concentration. ○ As calcium detaches from troponin, tropomyosin shifts back into place, blocking the myosin-binding sites on actin. Without active cross-bridge formation, the muscle relaxes. viii. Exercise and Aging Effects on Muscle (Expanded) 1. Effects of Exercise on Muscle: ○ Strength Training: Increases muscle mass through hypertrophy, which is the enlargement of existing muscle fibers. This occurs as resistance exercises cause small tears in muscle fibers, and during recovery, the body repairs and enlarges the fibers. Hypertrophy results from increased protein synthesis and the accumulation of contractile proteins (actin and myosin). Types of hypertrophy: Sarcoplasmic hypertrophy: Increases the volume of sarcoplasm, the fluid in muscle cells. Myofibrillar hypertrophy: Increases the size and number of myofibrils, the structures that house actin and myosin filaments. ○ Endurance Training: Increases the muscle’s ability to utilize oxygen efficiently by promoting mitochondrial biogenesis (an increase in the number and function of mitochondria) and enhancing capillary density. This allows muscles to generate ATP more efficiently through aerobic respiration. ○ Adaptation: With regular exercise, muscles become more resistant to fatigue due to improved metabolic efficiency and enhanced buffering capacity for lactate. 2. Effects of Aging on Muscle: ○ Sarcopenia: The loss of muscle mass, strength, and function due to aging. This typically begins after age 30 and accelerates with age. Causes: Sarcopenia is associated with reduced levels of growth hormones (e.g., testosterone, IGF-1), decreased physical activity, and the body's reduced ability to synthesize proteins. Mitochondrial dysfunction also plays a role. Effects: Reduced muscle mass leads to frailty, impaired mobility, and increased risk of falls and fractures. ○ Denervation of Muscle Fibers: Aging leads to a gradual loss of motor neurons, and thus, the muscles they innervate may atrophy. Surviving motor neurons attempt to re-innervate the denervated fibers, but this compensatory mechanism becomes less effective over time. ○ Prevention: Regular physical activity, especially resistance training, can help slow the progression of sarcopenia. Adequate nutrition, particularly protein intake, is crucial for maintaining muscle mass in aging individuals. xi. Energy Metabolism in Skeletal Muscle (Expanded) 1. Phosphocreatine (PCr) System: ○ The phosphocreatine system is the fastest way for muscles to regenerate ATP, but it can only sustain maximal effort for short bursts (~10-15 seconds). ○ In this system, the enzyme creatine kinase catalyzes the transfer of a phosphate group from phosphocreatine to ADP, quickly producing ATP: PCr+ADP→Creatine+ATP\text{PCr} + \text{ADP} \rightarrow \text{Creatine} + \text{ATP}PCr+ADP→Creatine+ATP ○ This system is essential for activities like sprinting or heavy lifting where immediate energy is required. 2. Anaerobic Glycolysis: ○ When oxygen is limited (as in intense exercise), muscles rely on anaerobic glycolysis to generate ATP. Glucose is broken down into pyruvate, and in the absence of oxygen, pyruvate is converted into lactate. This process generates 2 ATP molecules per glucose molecule. ○ Lactic acid accumulation can lead to muscle fatigue, but the body can convert lactate back to glucose via the Cori cycle in the liver. 3. Aerobic Respiration: ○ For sustained activity, muscle cells generate ATP through aerobic respiration, which takes place in the mitochondria. This process uses oxygen to fully oxidize glucose, fatty acids, or amino acids into CO₂ and H₂O, yielding 36-38 ATP per glucose molecule. ○ Fatty acids are the primary fuel source for long-duration, low-to-moderate intensity exercise. The beta-oxidation of fatty acids generates large amounts of ATP but requires oxygen. xv. Muscle Reflexes (Expanded) 1. Golgi Tendon Organ (GTO): ○ The Golgi tendon organ is a proprioceptive sensory receptor located at the junction between muscle fibers and tendons. Its primary function is to sense tension in the muscle-tendon unit. ○ When excessive tension is detected, the GTO sends inhibitory signals to the spinal cord, triggering the inverse stretch reflex. This reflex inhibits the muscle from contracting further, protecting it from damage or injury due to overexertion. ○ This mechanism is particularly important during high-force activities like heavy weightlifting, where the risk of muscle or tendon injury is higher. 2. Muscle Spindle Fibers: ○ Muscle spindles are sensory receptors located within the belly of the muscle. They are sensitive to changes in muscle length and the rate of lengthening. ○ When a muscle is stretched rapidly, the muscle spindles activate the stretch reflex (also known as the myotatic reflex), causing the muscle to contract to prevent overstretching. This reflex helps maintain muscle tone and posture. ○ For example, during the knee-jerk reflex (patellar reflex), tapping the patellar tendon stretches the quadriceps muscle, causing an immediate contraction of the muscle and a quick leg extension. Head and Neck Muscles 1. Frontalis: ○ Nerve Innervation: Facial nerve (CN VII, temporal branch) 2. Orbicularis Oris: ○ Nerve Innervation: Facial nerve (CN VII, buccal branch) 3. Orbicularis Oculi: ○ Nerve Innervation: Facial nerve (CN VII, temporal and zygomatic branches) 4. Occipitofrontalis (Occipitalis and Frontalis combined): ○ Nerve Innervation: Frontalis: Facial nerve (CN VII, temporal branch) Occipitalis: Facial nerve (CN VII, posterior auricular branch) 5. Zygomaticus Major: ○ Nerve Innervation: Facial nerve (CN VII, zygomatic and buccal branches) 6. Masseter: ○ Nerve Innervation: Mandibular nerve (branch of the Trigeminal nerve, CN V3) 7. Sternocleidomastoid: ○ Nerve Innervation: Accessory nerve (CN XI) and Cervical spinal nerves C2-C3 8. Trapezius: ○ Nerve Innervation: Accessory nerve (CN XI) and Cervical spinal nerves C3-C4 9. Buccinator: ○ Nerve Innervation: Facial nerve (CN VII, buccal branch) Muscles that Move the Upper Extremities 1. Pectoralis Major: ○ Nerve Innervation: Medial and lateral pectoral nerves (C5-C8, T1) 2. Latissimus Dorsi: ○ Nerve Innervation: Thoracodorsal nerve (C6-C8) 3. Deltoid: ○ Nerve Innervation: Axillary nerve (C5-C6) 4. Teres Major: ○ Nerve Innervation: Lower subscapular nerve (C5-C6) 5. Biceps Brachii: ○ Nerve Innervation: Musculocutaneous nerve (C5-C6) 6. Triceps Brachii: ○ Nerve Innervation: Radial nerve (C6-C8) 7. Brachialis: ○ Nerve Innervation: Musculocutaneous nerve (C5-C6), with some contribution from the Radial nerve 8. Brachioradialis: ○ Nerve Innervation: Radial nerve (C5-C6) 9. Palmaris Longus: ○ Nerve Innervation: Median nerve (C7-C8) 10. Flexor Carpi Radialis: ○ Nerve Innervation: Median nerve (C6-C7) 11. Flexor Digitorum Superficialis: ○ Nerve Innervation: Median nerve (C7, C8, T1) 12. Extensor Carpi Radialis: ○ Nerve Innervation: Radial nerve (C6-C7) 13. Extensor Digitorum: ○ Nerve Innervation: Radial nerve (posterior interosseous nerve, C7-C8) 14. Extensor Digiti Minimi: ○ Nerve Innervation: Radial nerve (posterior interosseous nerve, C7-C8) 15. Extensor Carpi Ulnaris: ○ Nerve Innervation: Radial nerve (posterior interosseous nerve, C7-C8) 16. Infraspinatus: ○ Nerve Innervation: Suprascapular nerve (C5-C6) 17. Supraspinatus: ○ Nerve Innervation: Suprascapular nerve (C5-C6) 18. Subscapularis: ○ Nerve Innervation: Upper and lower subscapular nerves (C5-C6) 19. Teres Minor: ○ Nerve Innervation: Axillary nerve (C5-C6) Muscles of the Trunk 1. External Intercostals: ○ Nerve Innervation: Intercostal nerves (T1-T11) 2. Internal Intercostals: ○ Nerve Innervation: Intercostal nerves (T1-T11) 3. Transverse Abdominis: ○ Nerve Innervation: Lower six thoracic nerves (T7-T12) and iliohypogastric and ilioinguinal nerves 4. Rectus Abdominis: ○ Nerve Innervation: Lower six thoracic nerves (T7-T12) 5. Serratus Anterior: ○ Nerve Innervation: Long thoracic nerve (C5-C7) 6. Diaphragm: ○ Nerve Innervation: Phrenic nerve (C3-C5) Muscles that Move the Lower Extremities 1. Iliopsoas: ○ Nerve Innervation: Psoas major: Lumbar plexus (L1-L3) Iliacus: Femoral nerve (L2-L4) 2. Sartorius: ○ Nerve Innervation: Femoral nerve (L2-L3) 3. Gluteus Maximus: ○ Nerve Innervation: Inferior gluteal nerve (L5, S1, S2) 4. Gluteus Medius: ○ Nerve Innervation: Superior gluteal nerve (L4, L5, S1) 5. Tensor Fasciae Latae: ○ Nerve Innervation: Superior gluteal nerve (L4, L5, S1) 6. Adductor Longus: ○ Nerve Innervation: Obturator nerve (L2-L4) 7. Gracilis: ○ Nerve Innervation: Obturator nerve (L2-L3) 8. Semimembranosus: ○ Nerve Innervation: Sciatic nerve (tibial portion, L5, S1, S2) 9. Semitendinosus: ○ Nerve Innervation: Sciatic nerve (tibial portion, L5, S1, S2) 10. Biceps Femoris: ○ Nerve Innervation: Long head: Sciatic nerve (tibial portion, L5, S1, S2) Short head: Sciatic nerve (common fibular portion, L5, S1, S2) 11. Rectus Femoris: ○ Nerve Innervation: Femoral nerve (L2-L4) 12. Vastus Lateralis: ○ Nerve Innervation: Femoral nerve (L2-L4) 13. Vastus Intermedius: ○ Nerve Innervation: Femoral nerve (L2-L4) 14. Vastus Medialis: ○ Nerve Innervation: Femoral nerve (L2-L4) 15. Tibialis Anterior: ○ Nerve Innervation: Deep fibular (peroneal) nerve (L4-L5) 16. Gastrocnemius: ○ Nerve Innervation: Tibial nerve (S1-S2) 17. Soleus: ○ Nerve Innervation: Tibial nerve (S1-S2) 18. Peroneus Longus: ○ Nerve Innervation: Superficial fibular (peroneal) nerve (L5, S1, S2) 19. Peroneus Brevis: ○ Nerve Innervation: Superficial fibular (peroneal) nerve (L5, S1, S2) MORE DETAIL ! IF TIME PERMITS Head and Neck Muscles 1. Frontalis: ○ Nerve Innervation: Facial nerve (CN VII, temporal branch) ○ Function: Elevates the eyebrows and wrinkles the forehead, expressing surprise or curiosity. The frontalis is part of the occipitofrontalis muscle, and it works with the occipitalis to move the scalp. ○ Anatomical Relationship: The facial nerve's temporal branch emerges from the stylomastoid foramen of the temporal bone, ascends to innervate the muscles of facial expression, including the frontalis. 2. Orbicularis Oris: ○ Nerve Innervation: Facial nerve (CN VII, buccal branch) ○ Function: Closes and puckers the lips, crucial for speech articulation, eating, and expressions like kissing. ○ Anatomical Relationship: The buccal branch of the facial nerve, passing through the parotid gland, innervates the muscles around the mouth. 3. Orbicularis Oculi: ○ Nerve Innervation: Facial nerve (CN VII, temporal and zygomatic branches) ○ Function: Closes the eyelids; involved in blinking and winking. Its palpebral portion helps with gentle closing (e.g., blinking), while the orbital portion allows tight closure (e.g., squinting). ○ Anatomical Relationship: The temporal and zygomatic branches of CN VII emerge from the parotid plexus and run over the zygomatic arch to reach the orbicularis oculi. 4. Occipitofrontalis (Frontalis + Occipitalis): ○ Frontalis (innervation): Facial nerve (CN VII, temporal branch) ○ Occipitalis (innervation): Facial nerve (CN VII, posterior auricular branch) ○ Function: Moves the scalp backward and forward, raises the eyebrows, and wrinkles the forehead. The frontalis and occipitalis portions are connected by the galea aponeurotica. ○ Anatomical Relationship: The posterior auricular nerve (a branch of CN VII) innervates the occipitalis muscle and passes behind the ear, while the temporal branch reaches the frontalis. 5. Zygomaticus Major: ○ Nerve Innervation: Facial nerve (CN VII, zygomatic and buccal branches) ○ Function: Elevates the corners of the mouth, producing a smile. ○ Anatomical Relationship: The zygomatic branch travels along the zygomatic arch, and the buccal branch courses anteriorly from the parotid gland to reach the zygomaticus major. 6. Masseter: ○ Nerve Innervation: Mandibular nerve (V3, a branch of the trigeminal nerve) ○ Function: Elevates the mandible, allowing for mastication (chewing). ○ Anatomical Relationship: The mandibular nerve passes through the foramen ovale to innervate the muscles of mastication, including the masseter. It works alongside other muscles like the temporalis. 7. Sternocleidomastoid: ○ Nerve Innervation: Accessory nerve (CN XI), with contributions from cervical spinal nerves C2-C3 ○ Function: Flexes the neck and rotates the head to the opposite side; both sides together cause neck flexion. ○ Anatomical Relationship: The accessory nerve descends from the jugular foramen and innervates the sternocleidomastoid and trapezius muscles. Cervical nerves contribute to proprioception. 8. Trapezius: ○ Nerve Innervation: Accessory nerve (CN XI), with contributions from C3-C4 spinal nerves ○ Function: Elevates, retracts, and depresses the scapula; extends the neck. ○ Anatomical Relationship: CN XI innervates the trapezius after passing the jugular foramen, traveling along the posterior triangle of the neck, and receiving contributions from C3-C4 for sensory input. 9. Buccinator: ○ Nerve Innervation: Facial nerve (CN VII, buccal branch) ○ Function: Compresses the cheeks, as in blowing or sucking; helps keep food between the teeth during chewing. ○ Anatomical Relationship: The buccal branch of CN VII passes forward to reach the buccinator muscle, forming part of the facial musculature that contributes to expressions and oral functions. Muscles that Move the Upper Extremities 1. Pectoralis Major: ○ Nerve Innervation: Medial and lateral pectoral nerves (C5-C8, T1) ○ Function: Adducts, medially rotates, and flexes the humerus. ○ Anatomical Relationship: The lateral pectoral nerve originates from the lateral cord of the brachial plexus, while the medial pectoral nerve originates from the medial cord. These nerves innervate both the clavicular and sternal heads of the pectoralis major. 2. Latissimus Dorsi: ○ Nerve Innervation: Thoracodorsal nerve (C6-C8) ○ Function: Extends, adducts, and medially rotates the humerus. ○ Anatomical Relationship: The thoracodorsal nerve is a branch of the posterior cord of the brachial plexus and descends along the posterior axillary wall to reach the latissimus dorsi. 3. Deltoid: ○ Nerve Innervation: Axillary nerve (C5-C6) ○ Function: Abducts the arm, with different fibers involved in flexion, extension, and rotation of the shoulder. ○ Anatomical Relationship: The axillary nerve arises from the posterior cord of the brachial plexus, travels through the quadrangular space, and wraps around the surgical neck of the humerus to innervate the deltoid. 4. Teres Major: ○ Nerve Innervation: Lower subscapular nerve (C5-C6) ○ Function: Adducts and medially rotates the humerus. ○ Anatomical Relationship: The lower subscapular nerve branches from the posterior cord of the brachial plexus and runs to the inferior part of the scapula to innervate the teres major. 5. Biceps Brachii: ○ Nerve Innervation: Musculocutaneous nerve (C5-C6) ○ Function: Flexes the elbow and supinates the forearm. ○ Anatomical Relationship: The musculocutaneous nerve, arising from the lateral cord of the brachial plexus, pierces the coracobrachialis and descends between the biceps brachii and brachialis. 6. Triceps Brachii: ○ Nerve Innervation: Radial nerve (C6-C8) ○ Function: Extends the elbow. ○ Anatomical Relationship: The radial nerve travels in the radial groove of the humerus to innervate the triceps brachii, branching into the lateral and medial heads of the muscle. 7. Brachialis: ○ Nerve Innervation: Musculocutaneous nerve (C5-C6), with some contribution from the radial nerve (C7) ○ Function: Flexes the elbow. ○ Anatomical Relationship: The musculocutaneous nerve runs through the brachialis, while the radial nerve provides minor innervation to the lateral part of the muscle. 8. Brachioradialis: ○ Nerve Innervation: Radial nerve (C5-C6) ○ Function: Flexes the elbow, especially in a mid-pronated position. ○ Anatomical Relationship: The radial nerve branches off into the brachioradialis as it travels down the lateral aspect of the forearm. 9. Palmaris Longus: ○ Nerve Innervation: Median nerve (C7-C8) ○ Function: Flexes the wrist and tenses the palmar aponeurosis. ○ Anatomical Relationship: The median nerve travels through the forearm between the flexor digitorum superficialis and flexor digitorum profundus, innervating the palmaris longus as it passes through the carpal tunnel. 10. Flexor Carpi Radialis: ○ Nerve Innervation: Median nerve (C6-C7) ○ Function: Flexes and abducts the wrist. ○ Anatomical Relationship: The median nerve runs down the anterior forearm alongside the radial artery, supplying the flexor carpi radialis, which is located medial to the brachioradialis. 11. Flexor Digitorum Superficialis: ○ Nerve Innervation: Median nerve (C7, C8, T1) ○ Function: Flexes the middle phalanges of the fingers (proximal interphalangeal joints) and the wrist. ○ Anatomical Relationship: The median nerve innervates this muscle, which lies deep to the palmaris longus and flexor carpi radialis. It splits into four tendons that pass through the carpal tunnel to reach the fingers. 12. Extensor Carpi Radialis: ○ Nerve Innervation: Radial nerve (C6-C7) ○ Function: Extends and abducts the wrist. ○ Anatomical Relationship: The radial nerve innervates the extensor carpi radialis longus and brevis, which run along the lateral side of the forearm. 13. Extensor Digitorum: ○ Nerve Innervation: Radial nerve (posterior interosseous nerve, C7-C8) ○ Function: Extends the fingers and the wrist. ○ Anatomical Relationship: The posterior interosseous nerve (a branch of the radial nerve) innervates the extensor digitorum, which sends tendons to the dorsal surfaces of the fingers. 14. Extensor Digiti Minimi: ○ Nerve Innervation: Radial nerve (posterior interosseous nerve, C7-C8) ○ Function: Extends the little finger and assists with wrist extension. ○ Anatomical Relationship: The posterior interosseous nerve innervates this small muscle, which lies medial to the extensor digitorum. 15. Extensor Carpi Ulnaris: ○ Nerve Innervation: Radial nerve (posterior interosseous nerve, C7-C8) ○ Function: Extends and adducts the wrist. ○ Anatomical Relationship: This muscle runs along the ulnar side of the forearm, with innervation coming from the posterior interosseous nerve, which travels in the posterior compartment of the forearm. 16. Infraspinatus: ○ Nerve Innervation: Suprascapular nerve (C5-C6) ○ Function: Laterally rotates the arm; stabilizes the shoulder joint. ○ Anatomical Relationship: The suprascapular nerve, originating from the upper trunk of the brachial plexus, passes through the suprascapular notch to reach the infraspinatus. 17. Supraspinatus: ○ Nerve Innervation: Suprascapular nerve (C5-C6) ○ Function: Initiates abduction of the arm (first 15 degrees) and assists in stabilizing the shoulder. ○ Anatomical Relationship: The suprascapular nerve innervates both the supraspinatus and infraspinatus, passing beneath the acromion of the scapula. 18. Subscapularis: ○ Nerve Innervation: Upper and lower subscapular nerves (C5-C6) ○ Function: Medially rotates the arm; stabilizes the shoulder joint. ○ Anatomical Relationship: The upper and lower subscapular nerves arise from the posterior cord of the brachial plexus and supply the subscapularis, which forms part of the rotator cuff. 19. Teres Minor: ○ Nerve Innervation: Axillary nerve (C5-C6) ○ Function: Laterally rotates the arm and helps stabilize the shoulder joint. ○ Anatomical Relationship: The axillary nerve, after passing through the quadrangular space, innervates the teres minor. It runs alongside the posterior circumflex humeral artery. Muscles of the Trunk 1. External Intercostals: ○ Nerve Innervation: Intercostal nerves (T1-T11) ○ Function: Elevates the ribs during inspiration, increasing the thoracic cavity's volume. ○ Anatomical Relationship: The intercostal nerves are the ventral rami of thoracic spinal nerves, running in the intercostal spaces to innervate the external intercostals. 2. Internal Intercostals: ○ Nerve Innervation: Intercostal nerves (T1-T11) ○ Function: Depresses the ribs during forced expiration, decreasing thoracic volume. ○ Anatomical Relationship: The internal intercostals are innervated by the same intercostal nerves as the external intercostals but are located deeper within the rib cage. 3. Transverse Abdominis: ○ Nerve Innervation: Lower six thoracic nerves (T7-T12), iliohypogastric nerve, and ilioinguinal nerve ○ Function: Compresses abdominal contents, providing thoracic and pelvic stability. ○ Anatomical Relationship: The transverse abdominis is the deepest of the abdominal muscles and is innervated by thoracoabdominal nerves (lower intercostal nerves) and branches of the lumbar plexus. 4. Rectus Abdominis: ○ Nerve Innervation: Lower six thoracic nerves (T7-T12) ○ Function: Flexes the vertebral column and compresses the abdomen. ○ Anatomical Relationship: The rectus abdominis lies within the rectus sheath and is segmentally innervated by the lower thoracic nerves. 5. Serratus Anterior: ○ Nerve Innervation: Long thoracic nerve (C5-C7) ○ Function: Protracts and stabilizes the scapula, assisting in upward rotation. ○ Anatomical Relationship: The long thoracic nerve travels superficially along the serratus anterior, making it vulnerable to injury, which can result in a condition known as "winged scapula." 6. Diaphragm: ○ Nerve Innervation: Phrenic nerve (C3-C5) ○ Function: Primary muscle of respiration, contracting to increase the volume of the thoracic cavity during inhalation. ○ Anatomical Relationship: The phrenic nerve descends from the cervical plexus, running along the pericardium to reach the diaphragm. It also carries sensory information from the central tendon of the diaphragm. Muscles that Move the Lower Extremities 1. Iliopsoas: ○ Nerve Innervation: Psoas major: Lumbar plexus (L1-L3), Iliacus: Femoral nerve (L2-L4) ○ Function: Flexes the hip joint, bringing the thigh toward the torso. ○ Anatomical Relationship: The lumbar plexus supplies the psoas major, while the femoral nerve innervates the iliacus, which together form the iliopsoas, the most powerful hip flexor. 2. Sartorius: ○ Nerve Innervation: Femoral nerve (L2-L3) ○ Function: Flexes, abducts, and laterally rotates the thigh at the hip joint; also flexes the knee. ○ Anatomical Relationship: The femoral nerve travels through the femoral triangle to reach the sartorius, the longest muscle in the body, running obliquely across the thigh. 3. Gluteus Maximus: ○ Nerve Innervation: Inferior gluteal nerve (L5, S1, S2) ○ Function: Extends and laterally rotates the thigh; helps with rising from a sitting position. ○ Anatomical Relationship: The inferior gluteal nerve emerges from the sacral plexus and exits the pelvis through the greater sciatic foramen to innervate the gluteus maximus. 4. Gluteus Medius: ○ Nerve Innervation: Superior gluteal nerve (L4, L5, S1) ○ Function: Abducts and medially rotates the thigh; stabilizes the pelvis during walking. ○ Anatomical Relationship: The superior gluteal nerve emerges from the sacral plexus and travels through the greater sciatic foramen superior to the piriformis to innervate the gluteus medius. 5. Tensor Fasciae Latae: ○ Nerve Innervation: Superior gluteal nerve (L4, L5, S1) ○ Function: Abducts and medially rotates the thigh; tenses the fascia lata, aiding in hip stability and knee extension. ○ Anatomical Relationship: Like the gluteus medius, the tensor fasciae latae is innervated by the superior gluteal nerve, with the nerve running along the lateral aspect of the hip. 6. Adductor Longus: ○ Nerve Innervation: Obturator nerve (L2-L4) ○ Function: Adducts the thigh and assists in medial rotation. ○ Anatomical Relationship: The obturator nerve passes through the obturator foramen to innervate the adductor longus, located medially on the thigh. 7. Gracilis: ○ Nerve Innervation: Obturator nerve (L2-L3) ○ Function: Adducts the thigh, flexes the knee, and medially rotates the leg. ○ Anatomical Relationship: The gracilis is a long, slender muscle located on the medial side of the thigh, with the obturator nerve innervating it after emerging from the pelvis. 8. Semimembranosus: ○ Nerve Innervation: Tibial part of the sciatic nerve (L5, S1-S2) ○ Function: Extends the thigh and flexes the knee; also medially rotates the leg. ○ Anatomical Relationship: The tibial portion of the sciatic nerve, descending through the posterior compartment of the thigh, innervates this hamstring muscle. 9. Semitendinosus: ○ Nerve Innervation: Tibial part of the sciatic nerve (L5, S1-S2) ○ Function: Extends the thigh and flexes the knee; also medially rotates the leg. ○ Anatomical Relationship: The semitendinosus is located superficially to the semimembranosus, with the tibial part of the sciatic nerve innervating both muscles. 10. Biceps Femoris: ○ Nerve Innervation: Long head: Tibial part of the sciatic nerve (L5, S1-S2); Short head: Common fibular nerve (L5, S1-S2) ○ Function: Flexes the knee and extends the thigh; laterally rotates the leg. ○ Anatomical Relationship: The biceps femoris is composed of two heads with different innervations. The long head is innervated by the tibial division, while the short head is innervated by the common fibular (peroneal) division of the sciatic nerve. 11. Rectus Femoris: ○ Nerve Innervation: Femoral nerve (L2-L4) ○ Function: Extends the knee and flexes the hip. ○ Anatomical Relationship: The femoral nerve innervates this biarticular muscle, which is part of the quadriceps group. It runs through the anterior thigh, innervating the rectus femoris as it crosses both the hip and knee joints. 12. Vastus Lateralis: ○ Nerve Innervation: Femoral nerve (L2-L4) ○ Function: Extends the knee. ○ Anatomical Relationship: The vastus lateralis, the largest part of the quadriceps group, is innervated by the femoral

Anatomy and Physiology of the Integumentary System (PDF)

Document Details

Tags

Related

Summary

Full Transcript

Upgrade to continue