Podcast
Questions and Answers
What is the primary cause of hyperpituitarism?
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?
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?
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?
What oral manifestation is associated with hypothyroidism?
Parathyroid hormone (PTH) plays a role in:
Parathyroid hormone (PTH) plays a role in:
Oral manifestations of hyperparathyroidism may include:
Oral manifestations of hyperparathyroidism may include:
What is the primary characteristic of diabetes mellitus?
What is the primary characteristic of diabetes mellitus?
Type 1 Diabetes results from:
Type 1 Diabetes results from:
What oral complication is commonly associated with uncontrolled diabetes mellitus?
What oral complication is commonly associated with uncontrolled diabetes mellitus?
What is a significant clinical marker for diabetes that dentists and hygienists should recognize?
What is a significant clinical marker for diabetes that dentists and hygienists should recognize?
What is Addison's Disease?
What is Addison's Disease?
What causes the bronzing of the skin and melanotic macules on the oral mucosa in Addison's disease?
What causes the bronzing of the skin and melanotic macules on the oral mucosa in Addison's disease?
What is a common sign of Cushing Syndrome?
What is a common sign of Cushing Syndrome?
What is the primary characteristic of anemia?
What is the primary characteristic of anemia?
Angular cheilitis, pallor of the oral mucosa and atrophy of tongue papilla are oral manifestations associated with:
Angular cheilitis, pallor of the oral mucosa and atrophy of tongue papilla are oral manifestations associated with:
What condition may result from long-standing iron deficiency anemia?
What condition may result from long-standing iron deficiency anemia?
Pernicious anemia is caused by a deficiency in:
Pernicious anemia is caused by a deficiency in:
What oral manifestation is associated with pernicious anemia?
What oral manifestation is associated with pernicious anemia?
Which population is most commonly affected by Sickle Cell Anemia?
Which population is most commonly affected by Sickle Cell Anemia?
Oral radiographs of a patient with sickle cell anemia may reveal:
Oral radiographs of a patient with sickle cell anemia may reveal:
What is the primary characteristic of aplastic anemia?
What is the primary characteristic of aplastic anemia?
What oral manifestation is associated with aplastic anemia?
What oral manifestation is associated with aplastic anemia?
What characterizes polycythemia?
What characterizes polycythemia?
Which oral manifestation is associated with polycythemia?
Which oral manifestation is associated with polycythemia?
What is the purpose of monitoring INR values in patients taking Warfarin?
What is the purpose of monitoring INR values in patients taking Warfarin?
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:
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:
A significant reduction in circulating neutrophils is a characteristic of:
A significant reduction in circulating neutrophils is a characteristic of:
What oral infection is associated with Agranulocytosis?
What oral infection is associated with Agranulocytosis?
Leukemia is a type of cancer that is characterized by:
Leukemia is a type of cancer that is characterized by:
What is a common oral manifestation of leukemia?
What is a common oral manifestation of leukemia?
The most common form of chronic leukemia is:
The most common form of chronic leukemia is:
A painful burning tongue, atrophy of papillae of the tongue and ulcerations of the oral mucosa are oral manifestations of:
A painful burning tongue, atrophy of papillae of the tongue and ulcerations of the oral mucosa are oral manifestations of:
What is a potential side effect of cancer radiation therapy affecting the salivary glands, causing dry mouth?
What is a potential side effect of cancer radiation therapy affecting the salivary glands, causing dry mouth?
What oral condition can Phenytoin, Nifedipine and cyclosporine cause?
What oral condition can Phenytoin, Nifedipine and cyclosporine cause?
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?
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?
Why do cancer patients treated with antiresorptive medications have a 100x greater chance of devolping ONJ than osteoporosis patients treated with those same medications?
Why do cancer patients treated with antiresorptive medications have a 100x greater chance of devolping ONJ than osteoporosis patients treated with those same medications?
Why do you consider vitamin D deficiency to be among the many hypothesis for medication-related Osteonecrosis of the Jaw?
Why do you consider vitamin D deficiency to be among the many hypothesis for medication-related Osteonecrosis of the Jaw?
What antibiotic is known to induce mucosal discoloration?
What antibiotic is known to induce mucosal discoloration?
Which of the following conditions results from excessive secretion of parathyroid hormone (PTH)?
Which of the following conditions results from excessive secretion of parathyroid hormone (PTH)?
One important treatment of agranulocytosis is:
One important treatment of agranulocytosis is:
Flashcards
Hyperpituitarism
Hyperpituitarism
Excess hormone production by the anterior pituitary gland, often from a benign tumor.
Hyperthyroidism
Hyperthyroidism
A condition resulting from excess thyroid hormone production.
Hypothyroidism
Hypothyroidism
Decreased output of thyroid hormone, leading to cretinism in children and myxedema in adults.
Hyperparathyroidism
Hyperparathyroidism
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Diabetes Mellitus
Diabetes Mellitus
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Ketoacidosis
Ketoacidosis
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What can ketoacidosis lead to?
What can ketoacidosis lead to?
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Addison Disease
Addison Disease
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Cushing Syndrome
Cushing Syndrome
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Anemia
Anemia
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Plummer-Vinson syndrome
Plummer-Vinson syndrome
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Thalassemia
Thalassemia
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Sickle Cell Anemia
Sickle Cell Anemia
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Aplastic Anemia
Aplastic Anemia
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Polycythemia
Polycythemia
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Agranulocytosis
Agranulocytosis
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Leukemia
Leukemia
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Celiac Disease
Celiac Disease
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Hemostasis
Hemostasis
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Purpura
Purpura
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Thrombocytopenic Purpura
Thrombocytopenic Purpura
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What can Vitamin C deficiency cause?
What can Vitamin C deficiency cause?
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Hemophilia
Hemophilia
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Xerostomia
Xerostomia
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Medication-Induced Mucosal Pigmentation
Medication-Induced Mucosal Pigmentation
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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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