Oral Pathology: Systemic Diseases

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Questions and Answers

What is the primary cause of hyperpituitarism?

  • A severe head trauma damaging the anterior pituitary
  • Genetic mutation causing overproduction of pituitary hormones
  • Autoimmune dysfunction affecting the pituitary gland
  • A benign tumor (pituitary adenoma) that produces growth hormone (correct)

What can hyperthyroidism lead to in children?

  • Premature exfoliation of deciduous teeth and premature eruption of permanent teeth (correct)
  • Increased density of the alveolar bone
  • Delayed exfoliation of deciduous teeth and delayed eruption of permanent teeth
  • Decreased risk of caries and periodontal disease

Which autoimmune disorder is the most common cause of hyperthyroidism?

  • Addison's disease
  • Hashimoto's thyroiditis
  • Cushing's syndrome
  • Graves' disease (correct)

What oral manifestation is associated with hypothyroidism?

<p>Enlarged tongue (D)</p> Signup and view all the answers

Parathyroid hormone (PTH) plays a role in:

<p>Calcium and phosphorus metabolism (B)</p> Signup and view all the answers

Oral manifestations of hyperparathyroidism may include:

<p>Well-defined radiolucencies (B)</p> Signup and view all the answers

What is the primary characteristic of diabetes mellitus?

<p>Abnormally high blood glucose levels (C)</p> Signup and view all the answers

Type 1 Diabetes results from:

<p>Autoimmune destruction of insulin-producing cells (D)</p> Signup and view all the answers

What oral complication is commonly associated with uncontrolled diabetes mellitus?

<p>Xerostomia (A)</p> Signup and view all the answers

What is a significant clinical marker for diabetes that dentists and hygienists should recognize?

<p>Periodontal disease (B)</p> Signup and view all the answers

What is Addison's Disease?

<p>Insufficient production of adrenal steroids (C)</p> Signup and view all the answers

What causes the bronzing of the skin and melanotic macules on the oral mucosa in Addison's disease?

<p>Stimulation of melanocytes (B)</p> Signup and view all the answers

What is a common sign of Cushing Syndrome?

<p>Weight gain (D)</p> Signup and view all the answers

What is the primary characteristic of anemia?

<p>Reduced oxygen-carrying capacity of blood (D)</p> Signup and view all the answers

Angular cheilitis, pallor of the oral mucosa and atrophy of tongue papilla are oral manifestations associated with:

<p>Anemia (A)</p> Signup and view all the answers

What condition may result from long-standing iron deficiency anemia?

<p>Plummer-Vinson Syndrome (B)</p> Signup and view all the answers

Pernicious anemia is caused by a deficiency in:

<p>Vitamin B12 (C)</p> Signup and view all the answers

What oral manifestation is associated with pernicious anemia?

<p>Painful, atrophic, and erythematous mucosa (B)</p> Signup and view all the answers

Which population is most commonly affected by Sickle Cell Anemia?

<p>Predominantly in black individuals and those of Mediterranean or Asian origin (A)</p> Signup and view all the answers

Oral radiographs of a patient with sickle cell anemia may reveal:

<p>Loss of trabeculation and large, irregular marrow spaces (A)</p> Signup and view all the answers

What is the primary characteristic of aplastic anemia?

<p>Severe depression of bone marrow activity causing a decrease in all circulating blood cells (C)</p> Signup and view all the answers

What oral manifestation is associated with aplastic anemia?

<p>Spontaneous bleeding (A)</p> Signup and view all the answers

What characterizes polycythemia?

<p>An increase in the number of circulating RBCs (B)</p> Signup and view all the answers

Which oral manifestation is associated with polycythemia?

<p>Deep red to purple oral mucosa (A)</p> Signup and view all the answers

What is the purpose of monitoring INR values in patients taking Warfarin?

<p>To measure Prothrombin time (A)</p> Signup and view all the answers

A reddish-blue or purplish discoloration of the skin or mucosa caused by spontaneous extravasation of blood, wich is seen in bleeding disorders is called:

<p>Purpura (D)</p> Signup and view all the answers

A significant reduction in circulating neutrophils is a characteristic of:

<p>Agranulocytosis (A)</p> Signup and view all the answers

What oral infection is associated with Agranulocytosis?

<p>Oral necrotizing ulcerations (B)</p> Signup and view all the answers

Leukemia is a type of cancer that is characterized by:

<p>Excessive number of abnormal WBCs (B)</p> Signup and view all the answers

What is a common oral manifestation of leukemia?

<p>Gingival enlargement caused by infiltration of leukemic cells (D)</p> Signup and view all the answers

The most common form of chronic leukemia is:

<p>Chronic lymphocytic leukemia (B)</p> Signup and view all the answers

A painful burning tongue, atrophy of papillae of the tongue and ulcerations of the oral mucosa are oral manifestations of:

<p>Celiac Disease (D)</p> Signup and view all the answers

What is a potential side effect of cancer radiation therapy affecting the salivary glands, causing dry mouth?

<p>Xerostomia (C)</p> Signup and view all the answers

What oral condition can Phenytoin, Nifedipine and cyclosporine cause?

<p>Gingival enlargement (C)</p> Signup and view all the answers

What could you consider a patient to have if they had a history containing an antiresorptive agent, exposed bone or bone that can be probed through an intraoral or extraoral fistula that has persisted at least 8 weeks and no history of radiation therapy to the jaws?

<p>MRONJ (C)</p> Signup and view all the answers

Why do cancer patients treated with antiresorptive medications have a 100x greater chance of devolping ONJ than osteoporosis patients treated with those same medications?

<p>The dosage requirement is significantly different between the 2. (C)</p> Signup and view all the answers

Why do you consider vitamin D deficiency to be among the many hypothesis for medication-related Osteonecrosis of the Jaw?

<p>Vitamin D is important in the immune system (B)</p> Signup and view all the answers

What antibiotic is known to induce mucosal discoloration?

<p>Minocycline (B)</p> Signup and view all the answers

Which of the following conditions results from excessive secretion of parathyroid hormone (PTH)?

<p>Hyperparathyroidism (D)</p> Signup and view all the answers

One important treatment of agranulocytosis is:

<p>Removal of the cause for the secondary form (C)</p> Signup and view all the answers

Flashcards

Hyperpituitarism

Excess hormone production by the anterior pituitary gland, often from a benign tumor.

Hyperthyroidism

A condition resulting from excess thyroid hormone production.

Hypothyroidism

Decreased output of thyroid hormone, leading to cretinism in children and myxedema in adults.

Hyperparathyroidism

Excessive secretion of parathyroid hormone (PTH), affecting calcium and phosphorus metabolism.

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Diabetes Mellitus

Chronic disorder of carbohydrate metabolism with abnormally high blood glucose levels.

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Ketoacidosis

Breakdown of fatty tissue leading to production of ketone acid, lowering blood pH, and potentially causing coma and death.

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What can ketoacidosis lead to?

An acute condition that can lead to coma and death

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Addison Disease

Addison disease results from insufficient production of adrenal steroids,

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Cushing Syndrome

Sustained increase in glucocorticosteroid levels.

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Anemia

A reduction in the oxygen-carrying capacity of blood, often related to decreased RBCs.

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Plummer-Vinson syndrome

Syndrome resulting from long-standing iron deficiency anemia, characterized by dysphagia, glossitis, and angular cheilitis.

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Thalassemia

A group of inherited disorders of hemoglobin synthesis

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Sickle Cell Anemia

An inherited blood disorder, predominantly in black individuals

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Aplastic Anemia

A severe depression of bone marrow activity, causing a decrease in all circulating blood cells (pancytopenia).

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Polycythemia

Increase in the number of circulating RBCs.

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Agranulocytosis

Significant reduction in circulating neutrophils.

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Leukemia

Malignant neoplasms of hematopoietic (blood-forming) stem cells, characterized by an excessive number of abnormal WBCs in circulating blood.

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Celiac Disease

Chronic disorder associated with sensitivity to dietary gluten.

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Hemostasis

Cessation of bleeding.

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Purpura

Reddish-blue or purplish discoloration of skin or mucosa from spontaneous extravasation of blood.

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Thrombocytopenic Purpura

A bleeding disorder resulting from a severe reduction in circulating platelets.

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What can Vitamin C deficiency cause?

Vitamin C deficiency may cause alterations in vascular walls, bleeding problems

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Hemophilia

A disorder of blood coagulation resulting in severely prolonged clotting time

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Xerostomia

Destruction of major salivary glands may result in this condition.

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Medication-Induced Mucosal Pigmentation

Discoloration resulting from medication

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Study Notes

Oral Pathology for the Dental Hygienist Introduction

  • This study guide is for Oral Pathology for the Dental Hygienist, 8th Edition, Chapter 9, Student Handout.
  • The chapter discusses oral manifestations of systemic diseases.

Oral Manifestations of Systemic Diseases

  • Many systemic diseases manifest in the oral mucosa, maxilla, and mandible.
  • Immunodeficiency can cause infection and neoplasia.
  • Systemic diseases and drugs used to treat them can impact oral tissue.
  • Local factors can exacerbate the oral manifestation of systemic disease.
  • Mild irritation and chronic inflammation may cause lesions.
  • Systemic diseases discussed include endocrine disorders, blood cell and platelet disorders and immunodeficiency disorders.

Endocrine Disorders

  • Involve integrated glands and cells secreting hormones
  • Hormone levels in blood trigger factors that control production
  • Diseases may result from too much or too little hormone production, gland dysfunction or problems with hormone control

Hyperpituitarism

  • Excess hormone production happens in the anterior pituitary gland
  • Benign tumors often cause it
  • Gigantism happens before the closure of long bones
  • In adult life acromegaly happens when hypersecretion occurs

Clinical Features and Oral Manifestations of Hyperpituitarism

  • Poor vision and light sensitivity are signs
  • Hands and feet enlarge and rib size increases
  • Facial features change
  • Enlargement of the maxilla and mandible may cause teeth separation and malocclusion
  • Frontal bossing and nasal bone enlargement is possible
  • Enlargement of the maxillary sinus leads to voice deepening
  • Mucosal changes can include thickened lips and macroglossia

Diagnosis and Treatment of Hyperpituitarism

  • Diagnosis involves measurement of growth hormone
  • Normal: Decrease in growth hormone
  • Acromegaly: Growth hormone will not decrease
  • Treatment includes pituitary gland surgery, medical management and radiation therapy
  • Diabetes, cardiovascular and respiratory diseases, and colon cancer can arise if untreated

Hyperthyroidism

  • Excess thyroid hormone production is also called thyrotoxicosis
  • More common in women in their 30s and 40s
  • Graves is the most common cause of hyperthyroidism
  • Graves is an autoimmune disorder where antibodies stimulate thyroid cells to produce too much thyroid hormone, enlarging the thyroid gland

Clinical Features of Hyperthyroidism

  • Thyroid enlargement (goiter)
  • Rosy complexion, erythema
  • Excessive sweating and fine hair is possible
  • Softened nails and exophthalmos can occur
  • Anxiety, weakness, restlessness, and cardiac problems may also be associated

Oral Manifestations of Hyperthyroidism

  • Premature exfoliation of deciduous teeth and eruption of permanent teeth may happen in children
  • Osteoporosis may affect alveolar bone, and burning tongue is also a symptom
  • Caries and periodontal disease may appear and develop rapidly in these patients

Treatment of Hyperthyroidism

  • Treatment includes surgery
  • Medications to suppress thyroid activity
  • Administration of radioactive iodine
  • Clinical mismanagement may lead to hypothyroidism

Hypothyroidism

  • A decreased the output of thyroid hormone
  • Cretinism occurs in infancy and childhood
  • Myxedema occurs in older children and adults
  • Causes iodine deficiency and developmental disturbances
  • Autoimmune destruction of thyroid: Hashimoto thyroiditis
  • Drugs and treatment for hyperthyroidism can cause this

Hypothyroidism: Oral Manifestations

  • Infants get thickened lips and tongue and delayed eruption of teeth
  • Enlarged tongue in adults

Hyperparathyroidism

  • Excessive secretion of parathyroid hormone (PTH) from the parathyroid glands
  • PTH roles include calcium and phosphorus metabolism
  • Elevated blood calcium levels, hypercalcemia
  • Low levels of blood phosphorus, hypophosphatemia
  • May be due to hyperplasia of parathyroid glands, benign or malignant tumor
  • More common in women than men and found in middle-aged adults

Clinical Features of Hyperparathyroidism

  • Mild cases may be asymptomatic, or may cause joint pain or stiffness
  • Lethargy, coma, kidney stones and can affect the skeletal and gastrointestinal system

Oral Manifestations of Hyperparathyroidism

  • Bone changes, and loosening of teeth
  • Well-defined unilocular or multilocular radiolucencies
  • "Ground glass" appearance, loss of lamina dura
  • Central giant cell granulomas (CGCGs) on a microscopic level

Diagnosis and Treatment of Hyperparathyroidism

  • Measurement of PTH blood levels, include serum calcium and phosphorus measurements
  • Treatment can correct increased hormone production due to tumors, renal disease, kidney failure, vitamin D deficiency

Diabetes Mellitus

  • High blood glucose levels characterize this chronic disorder of carbohydrate metabolism
  • High blood glucose levels, hyperglycemia caused by lack of insulin, defective insulin or resistance caused by obesity

Diabetes Mellitus and Glucose

  • Insulin is created by glucose signals in pancreas beta cells
  • Secreted in the bloodstream to facilitate glucose uptake into fat and skeletal muscle
  • Glucose can be used as an energy source
  • Cells starved without glucose results in break down of tissues, catabolism
  • Ketoacidosis, ketone acid, produced and lowers blood pH

Diabetes Mellitus: Ketoacidosis

  • Fatty tissue breaks down and ketone acid lowers blood pH
  • Acute condition can cause coma and death
  • Macrophages reduced, neutrophils delayed and lymphocytes affected
  • Collagen production is abnormal

Other Complications of Insulin-Dependent Diabetes Mellitus

  • Complications with organ systems damage blood vessels
  • Eyes: Blindness, Kidney: End-stage kidney failure, Nerves: Paresthesia or numbness
  • Atherosclerosis of large and medium-size blood vessels: Macrovascular disease
  • Abdominal aortic aneurysm, thrombi, stroke or cerebrovascular accident, myocardial Infarction

Diagnostic Criteria of Diabetes

  • Fasting blood glucose is equal to or greater than 126 mg/dL
  • A random blood glucose is equal to or greater than to 200 mg/dL
  • A 2-hour blood glucose level is also equal to or greater than 200 mg/dL after drinking a glucose solution of 75 grams
  • A glycosylated hemoglobin level is equal to or greater than 6.5%

Prediabetes

  • Fasting blood glucose is between 100 and 125mg/dL
  • Two-hour blood is between 140 and 199mg/dL after the OGTT
  • Glycosylated hemoglobin level is between 5.7% and 6.4%

Type 1 Diabetes

  • Autoimmune disease that destroys insulin-producing cells of the pancreas
  • 3% of all diabetic patients have this type, which can happen at any age, but it is more common is at 20 years of age
  • The peak age polydipsia- excessive thirst and intake of fluid occurs
  • Polyuria is excessive urination and excessive appetite, polyphagia
  • Treatment often involves multiple insulin injections and diet, exercise, and blood glucose level tests

Type 1 Diabetes and Hypoglycemia

  • Patients require insulin throughout their entire lives and the current approach to management of these patients involves frequent determination of blood glucose levels
  • Low blood sugar: Hypoglycemia = insulin shock
  • Uncontrolled blood glucose is brittle diabetes

Type 1 Diabetes Alternative Methods of Treatment

  • Methods to take in oral hypoglycemic medications and transplantation of pancreatic beta cells into the liver are viable
  • People can be treated by transplant of stem cells or usage of an insulin pump

Type 2 Diabetes

  • Characterized by insulin resistance
  • 97% of all diabetic patients have this type
  • Gradual onset that is usually present in patients 35-40 years of age or older, weight gain may contribute
  • Dentists and hygienists can play a role to educate patients

NIDDM and Obesity

  • Obesity decreases the number of receptors for insulin binding in fat and muscle
  • Adipokines are hormones produced from fatty tissue

Gestational Diabetes

  • Happens in pregnancy and disappears after pregnancy
  • Leads to macrosomia- increase in infant birth weight
  • The mother and child have a higher risk of developing type 2 diabetes later in life

Clinical Features of NIDDM

  • The vascular system is adversely affected
  • Decreased resistance to infection, skin infections, urinary tract infections (UTIs), and tuberculosis
  • Atherosclerosis, in blood vessel walls, causes impaired circulation
  • This increases the risk of ulceration, gangrene, stroke, high blood pressure and kidney failure

Clinical Features of NIDDM

  • Diabetic retinopathy in the eye can lead to blindness
  • The nervous system may be affected with decreased resistance to infection

Oral Complications of NIDDM

  • Oral candidiasis is possible
  • Mucormycosis: A rare oral fungal infection that affects the palate and maxillary sinuses
  • Bilateral asymptomatic parotid gland enlargement, xerostomia and periodontal disease can happen
  • An accentuated response to plaque formation and slow wound is also an issue

Considerations for Dentists and Dental Hygienists

  • Periodontal disease significant complication of diabetes, control is aggravated It poses significant prognostic/ predictive clinical marker for diabetes
  • Uncontrolled diabetes produces uncontrolled periodontal Conditions

Addison Diseases:

  • Addison disease (Primary Hypoadrenocorticism)- insufficient production of adrenal steroids
  • Causes include malignant tumor, tuberculosis, fungal infections, HIV
  • Autoimmune disease the pituitary gland increases adrenocorticotropic hormone (ACTH) to compensate
  • This may be caused by malignancies, tuberculosis, infections, autoimmunity

Clinical Features of Addison Disease

  • Melanocytes are stimulated
  • Bronzing of skin, melanotic macules on oral mucosa
  • Treatment includes steroid replacement therapy

Hypercortisolism (Cushing Syndrome)

  • Caused sustained increase in glucocorticosteroid levels signs will develop slowly
  • Weight gain obvious clinical feature
  • Hypertension and hyperglycemia is a sign
  • Decreased ability to respond to stress and mood alteration

Blood Disorders

  • Disorders of red blood cells (RBCs) and hemoglobin
  • Disorders of white blood cells (WBCs)
  • Bleeding disorders

Anemia

  • Reduction in the oxygen-carrying capacity of blood
  • Relates to a decrease in RBCs circulating
  • Nutritional anemias: Iron, folic acid, B12
  • Bone marrow stem cells gets suppressed

Clinical Features of Anemia

  • Pallor of skin and oral mucosa
  • Angular cheilitis and erythema in oral mucosa
  • Filiform and fungiform papillae are lost

Iron Deficiency Anemia

  • Insufficient amount of iron is supplied to bone marrow
  • Possible causes include deficient iron intake, blood loss, poor iron absorption, an increased requirement
  • Plummer Vinson syndrome is a result

Iron Deficiency Anemia: Plummer Vinson Syndrome

  • Long-standing iron deficiency anemia
  • Symptoms include nonspecific, shortness of breath, cardiac palpitations, and dysphagia
  • Tongue gets inflamed, glossitis and angular cheilitis caused by oral candidiasis
  • Can cause esophagus and oral cancer

Diagnosis and Treatment of Iron Deficiency Anemia

  • Laboratory tests show a low hemoglobin content and reduced hematocrit
  • Microcytic: Smaller-than-normal RBCs
  • Hypochromic: RBCs are lighter in color
  • Hematocrit: The volume of RBCs in blood
  • Treatment includes dietary supplements

Pernicious Anemia

  • A deficiency in intrinsic factor happens
  • Secreted by stomach parietal cells that absorption of vitamin B12
  • Autoimmune disorder
  • Might be caused by surgical stomach removal, cancer, or gastritis
  • B12 must be uptaken for DNA synthesis

Anemia: Clinical Features

  • Symptoms include weakness and pallor
  • Fatigue on exertion, nausea and dizziness
  • Diarrhea, and abdominal pain, loss in appetite and weight loss

Anemia: Oral Manifestations

  • Angular cheilitis and mucosal pallor, also atrophic and erythematous
  • Mucosal ulceration and loss of papillae on the dorsum of the tongue lead to soreness

Diagnosis and Treatment of Pernicious Anemia

  • Low serum B₁₂ levels and gastric achlorhydria (hydrochloric acid deficiency) are findings
  • Immature large RBCs,megaloblastic anemia and neutrophils/platelets are immature are all symptoms
  • The Schilling test indicates an inability to absorb oral vitamin B12
  • Serum antibodies present are directed against the intrinsic factor and vitamin B12 injections are the treatment

Deficiency Anemia

  • Folic acid and B12 come both can become dietary deficiencies
  • Commonly associated malnutrition; increased metabolic requirements
  • Usually found in correlation with alcoholism/pregnancy

Diagnosis and Treatment of Folic Acid and Vitamin B12 Deficiency Anemia

  • Labs test serum assays of folic acid and B12 and treatment is made up of dietary supplements
  • Megaloblastic anemias- presence of immature and large RBCs

Thalassemia

  • Genetic mutation of hemoglobin
  • Mediterranean or Cooley Anemia
  • Autosomal dominant inheritance pattern
  • Heterozygous - mildly symptomatic/asymptomatic
  • Homozygous- severe hemolytic anemia

Clinical Features and Oral Manifestations of Thalassemia

  • Yellow skin pallor and fever
  • Malaise and weakness
  • Enlarged spleen and liver, prominent cheekbones
  • Depression of the bridge of the nose, prominent maxilla, and circular radiolucencies in alveolar bone
  • Protrusion or flaring of maxillary anterior teeth, radiograph may show a salt-and-pepper pattern and thinning of lamina dura

Treatment of Thalassemia

  • Experimental and may involve blood transfusions and splenectomy
  • Poor prognosis, but getting better
  • Hemochromatosis: Deposition of excessive iron throughout body

Sickle Cell Anemia

  • Inherited blood disorder that occurs before a person's 30s
  • Common in black individuals, and those of Mediterranean or Asian origin
  • RBC's form a sickle shape with decreased oxygen
  • Triggered by exercise, exertion, administration of a general anesthetic, pregnancy, or even sleep

Sickle Cell Anemia: Clinical Features

  • Weakness, shortness of breath, fatigue, joint pain
  • Nausea, severe sickling of erythrocytes
  • Acute chest syndrome, kidney dysfunction, issues with the eyes, cardiovascular system, and CNS
  • Heart enlargement and cardiac failure are signs

Sickle Cell Anemia

  • Bones are characterized by a loss of trabeculation
  • Large, irregular marrow spaces appear & changes in skull trabeculae radiate outward

Diagnosis and Treatment of Sickle Cell Anemia

  • The sickle-shaped cells are seen on a blood smear
  • There is a low number of RBCs with low hemoglobin content
  • Oxygen is administered intravenously or orally as supportive treatment

Aplastic Anemia

  • Bone marrow severely depressed
  • Decrease in all circulating blood cells: Pancytopenia
  • Has unknown Primary aplastic anemia cause
  • From a drug/chemical agent

Clinical and Oral Manifestations of Aplastic Anemia

  • Present in various clinical signs, fatigue and weakness
  • Retinal/ cerebral hemorrhages. low platelets
  • Bruising, hematomas, ecchymosis
  • Predisposed to infections and oral infection
  • Spontaneous bleeding can happen, petechiae and purpuric spots

Diagnosis and Treatment of Aplastic Anemia

  • Labs show Leukopenia - low WBCs and Thrombocytopenia - Low platelets
  • Anemia is fatal and progress when removed
  • Aplastic treatment to eliminate cause

Polycythemia

  • Increase in the number of circulating RBCs
  • Three forms: primary, secondary, and relative

Polycythemia Vera

  • Neoplastic bone marrow causes increase RBC
  • Cause-unknown, it is commonly found in men
  • More known in white folks than in black individuals- aged between the 40-60s

Polycythemia Vera, Signs and symptoms

  • Headache, and dizziness are common symptoms
  • Disrupted circulation and itching of skin
  • vascular stasis and thrombocytopemia

Secondary Polycythemia

  • RBC increase, a physiologic reaction. from limited oxygen intake
  • High count erythropoietin kidneys
  • Caused by smoking, pulmonary cardiac, altitude and elevation in carbon monoxide/

Relative Polycythemia

  • Caused by a drop in plasma volume with vomiting, diarrhea, diuretics and profuse sweating
  • Middle-aged white men under physical stress are commonly diagnosed
  • Overweight, hypertensive with heavy smoking addiction

Polycythemia-Oral

  • Mouth show redness coloration between red and purple
  • Oral submucosa. with hematoma
  • Bleeding easily occur in the gingiva or from scratching

Diagnose-Treat Polycythemia

  • Examine hemoglobin measure- then lab test
  • Treatment include removing cause, Chemotherapy and Phlebotomy

White blood cell disorders

  • WBC disorders: infection-related conditions. bleeding disorder
  • Define: clinical aspect and oral manifestations
  • Diagnose celiac disease compare between acute and chronic leukemia

WBC disorders, bleeding, and oral cancer

  • Bleed. disorder with medication is understood and purpura has oral problems/symptoms
  • Medication like chem. and others
  • Understand function osteoblasts and osteoclasts

White Blood Cell Disorders

  • Group 3 in blood circular/ three groups of WBCs: Granulocytes, Lymphocytes, and Monocytes
Granulocytes in more detailed info:
  • Polymorphonuclear Leukocytes (or neutrophilic)
  • Eosinophils and basophils

Agranulocytosis

  • Decrease to where Neutropenia (low the neutrophil is occurring)
  • Primary where cause isn't found and the disorder is immunologic
  • Development of granulocytes is problematic, or granulocytes accelerated

Agranulocytosis-oral with signs and symptoms

  • Have and see symptoms like sudden chills, and jaundice with fever
  • Sore infection in the oral and jaundice
  • Destructive tooth, and swelling in the mouth, neck and all that around

Diagnose-Treat Agranulocytosis

  • By low WBC count, tests made
  • Then they transfuse it, and give antibiotics
  • Any procedure will be not needed for dental

Cyclic Neutropenia

  • Decrease cycle number neutrophils count
  • A condition oral has ulceration and issues

Leukemia

  • An issue when have a high WBC, and cancerous signs affect, like blood or body

Acute Leukemias

  • They are immature, or happen with a sudden fate, with needed treatment acute lymphoblastic is lymphocytic.

Symptoms for Acute and signs

  • Suddenness, dramatic or fatigue, or sudden
  • Or show sudden fever and lymph swell/enlargement
  • Thrombocytopenia means bleeding happens from the lymph

Oral Manifestations of and from Leukemia

  • Gums swelling
  • Bleeding can be from any area
  • Oral/ teeth will be affected

Acute Leuk Diagnose and Treatment

  • Blood test to determine to see platelet count and anemia present
  • treatment like bone marrow transplant is a possible solution

Chronic Leukemia

  • Chronic myeloid leukemia is associate Philadelphia
  • Lymphocytic form is familiar for a form-chronic

Leukemias signs/ symptoms

  • Symptoms slow to show up or present to show slow
  • Fatigueness and weakness show up with weight loss, which can lead to Anorexia

Anorexia-Oral sign- treat it and all its signs/ symptoms

  • Look at WBCs high levels
  • Transplants are a possible, Chemotherapy is also needed, and some cryotherapy may be recommended from your healthcare professional

Bleeding and Celiac Diseases and Oral Problems, Bleeding Disorder


  • Celiac Dis*

  • Sensitivity to what have to it, dietary gluten and you cant digestive it

  • Mouth will be burned/ affected with ulcer

  • Diarrhea can occur or nervousness as well too

Hemostasis, and Terminologies, all its signs, and symptoms/ tests, and disorders

  • Hemostats are good, and help with the wound and with clotting (its important that one happen, even if just a few)

  • Check-and make sure clot is good

  • Check to see platelet count, bleeding disorder will happen if count high

Tests like BLEEDING TIME

  • See adequacy of platelet and function
  • Make sure no bleeding during, function is adequate
  • Has 5 or 10 bleed depending on results

The PT test

  • See to make sure clot is good
  • Check normal in time frame and all those facts from it check out by second

Partial P-Time tests

  • To measure clot forming good
  • Used with/for heparin patients
  • To see if there is bleeding, a PTT test can show.

What we have Purpura

  • This is like when blood flows into the skin
  • There could be some issues
  • Capillaries weak, might have weakness

Thrombocytopenic Purpura's

  • Disorder happens when platelets or anything is really reduced or the amount its suppose to hold is decreased
  • Could be autoimmune related

Oral, and the signs from- Thrombocytopenic

  • Lesions and spontaneous with no irritation/harm
  • Have frequent nose and urination and all
  • Ecchymoses are a likely sign and a cause

Thromb thrombocytopenic test and care

  • Test how plates are working because important function
  • Some capillary test show and could be positive. Some- not good for you
  • Transfusions and dental can be good depending the condition

Non -THROMB

  • Vessels or plate problems lead here
  • Auto disease happen or issue with allergic/ and a chemical problem caused

Non , Oral/ care/ symptom

  • Some blisters occur
  • All this will be helped by discontinuing agent and taking something
  • Plate count to see

What hemophilia do?

  • Is when issue with or lack blood coagulation
  • From the disorder is that time is prolonged longer, where bleeding has no set time

Some factors with that Cascade and all

  • If have factor, that mean and what they mean to you
  • Factors are important because responsible for all

Different of Hemophilia

  • Daughter issue pass down to son-link from X disease
  • The A can have that one protein lacking from plasma, not much can be added. Also some Christmas has factor number.

How is The Mouth. showing oral -Hem

  • Shows gum show of it
  • Some cuts bleeding when do teeth scale with tool (dental) happens more often, and easily (oral) during

diagnose/ treat what has oral-hem

  • Bleed time and is normal
  • This to prolong, but the P is treat
  • Replace what is lost by finding (what test showed) what the case with oral-hem is for the patient

Therapies related, of those

  • Cancer and it’ Oral with radiation, surgery, with chemotherapy, and side too

  • Mucositis can occur- hurt and swell: start to happens 2 weeks later. Then over in 6 weeks!

What is a THERAPY? The radiation one? for the oral

  • Saliva is destroyed (too bad) and that causes xerostomia and all those issues relating bad

  • Care for patients- help the patient understand and fluoride

What is CHEMO? What effect it cause?

  • Side effect mucositis and cells affected, and oral ulcers can come

  • Some effects on basal epithelium cells

  • Complicate when it has Anemia and infections and that oral become hard to treat-for the patient

A drug -effect!

  • Blood medication can cause issues later
  • Can cause oral (fungal) too
  • Is caused by medicine to fix problems with other problems

Medication related or issue-related what is like those can be tested as-

  • Medication has the over suppression or infection in all, the parts for now
  • It leads bone to be affected when there bone die (more dead than bad)
  • There are three stage what happens during them

MRONJ- can form Mucosal discoloration

  • All these issues can cause pain and show signs in mouth, where is a good reminder to examine and know for the best care with health coming from.

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