Front | Back |
Polycythemia-
|
Erythrocytes are increased in number
|
Anemia
|
-deficiency in the erythrocytes abaility to transport oxygeb to and CO2 away from the tissues
¡Excessive blood loss from trauma, internal hemorrhage, or spontaneous hemolysis ¡Genetic diseases ¡Nutritional deficiencies |
Iron Deficiency Anemia
|
-Lack of red blood cells and hemoglobin because of indeaquate dietary intake of iron
- Tiredness, weakness, and malaise -Pale tissue pallor, glossitis, angular chelitis, apthous ulcerations |
Pernicious Anemia |
-Impaired red blood cell maturation secondary to B12 deficiency as a result of a defective intrinsic factor required for its absorption through the intestinal wall -Folic acid and B12 are needed for erythocytematuration -Deficiency caused by defective absorption factor (intrinsic factor) -Gasticmucosa is atrophic and fails to secrete hydrochloric acid — -Folateand B12 deficiency also cause megaloblasticanemia in which there is larger-than-normal red blood cells —Clincially- ¡Hunter’s glossitis- red tongue with atrophic filliformpapilla ¡Oral mucosa is atrophic and exhibit pallor, angular cheilitis |
Sickle Cell Anemia |
-Inherited defect in the structure of the hemoglobin molecule causing erythrocyte to assume a crescent “sickle” shape and undergo lysis -Primarily occurs in African and Mediterranean descent. It is also seen in people from South and Central America, the Caribbean, and the Middle East -Symptoms- malaise, weakness, yellowed sclera, muscle ridgidityand unconsciousness in sickle cell crisis. Wide spread ischemia may develop leading to death -Radiographically- numerous small icicle-like spiculesin the skull-cap (hair-on-end effect), stepladder trabeculaeare often seen between posterior teeth |
Thalassemia
|
-Inherited defect in either the alpha or beta chain of the hemoglobin molecule resulting in hemolysis -Most common in people of Meditteraneandescent -Hair-on-end in the skull cap bone, unusual “honeycomb” trabeculationin jaw |
Leukopenia
|
-Decrease ability to generate neutrophilsor reduction in neutrophils -Causes ¡Arrest in maturation of the cells of the bone marrow ¡Hematopoietic elements have been replaced ¡Pharmaceuticagents have inhibited cell cycling |
Agranulocytosis |
-A marked decrease in circulating granulocytes, particularylyneutrophils, attributable to a variety of causes -Neutrophilsare the first line in defense against bacterial infections -Can result in death because of secondary bacterial infection (pneumonia) -Clincally- oral ulcerations with chemotherapy at toxic levels causing white blood cell levels to drop. The lesions quickly progress to the bone with resultant osteomyleitisand sequestration |
Cyclic Neutrpenia |
-Idiopathic disease in which episodic fluctuation in the number of circulating neutrophilsand is due to a bone marrow maturation arrest -Children suffer from frequent recurrent respiratory infections -Apthous-like ulcers can occur within a few day of neutropenicphase -Premature periodontal disease is often encountered and children and teens may experience alveolar bonelossand periodontal pockets |
Neoplasms of Leukocytes
|
-Neoplastic process of leukocytes result in elevation of white blood cell count. These leukocytes are referred to as leukemias.
|
Leukemia
|
Circulating malignant leukoctes of bone marrow or lymph node orgin -Leukemias are categorized according to the stem cell of orgin ¡Myelogenous or granulocytic- bone marrow ¡Lymphocytic -Acute- rapidly progressing, usually fatal and tend to occur in children -Chronic- More often encountered in adults, potentially fatal, but may will undergo prolonged periods of remission with chemotherapy -Clinical features ¡Chronic fatigue and malaise ¡Petechiaesecondary to thrombocytopenia ¡Anemia ¡Fevers of unkownorigin or other infections of the UR or genitourinary tract ¡Orally- petechialhemorrhage and gingival enlargement in 10% |
Multiple Myeloma
|
-A disseminated (widely dispersed) neoplasm of differnetiatedB lymphocytes -Lymphoma -Arises in the 4th, 5thand 6thdecades -Usually goes unnoticed because it is asymptomatic until it is wide spread -Symptoms- deep bone pain due to osteolyticbone lesion -Radiographically- coin-shaped, punched-out lesions radiolucenciesand are prominent in the skull. Dental radiographs may also have punched-out lesions, but may have widespread osseous destruction with radiographic margins appear “moth-eaten” and teeth may be loose -Poor prognosis |
Thrombocytopenia |
-Platelet disorder -Decrease in number of circulating blood platelets that can be caused by a variety of factors -Caused by chemotherapeutics, leukemia and idiopathic thrombocytopenic purpurain HIV patients |
Hemophilia
|
-Hereditary coagulation disorders
-Purpurais purple-colored spots and patches that occur on the skin, organs, and in mucus membranes, including the lining of the mouth. (bruises, ecchymosis) -Acquired coagulopathy- associated with liver cirrhosis -Oral surgical procedures can be life threatening if appropriate precautions are not observed. -Hospitalization and coagulation factor supplement |