Pathology: Diseases of the Blood

Chapter 12

14 cards   |   Total Attempts: 186
  

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Cards In This Set

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
Question 4
Pernicious Anemia
Answer 4
-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
Question 5
Sickle Cell Anemia
Answer 5
-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
Answer 6
-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
Question 8
Agranulocytosis
Answer 8
-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
Question 9
Cyclic Neutrpenia
Answer 9
-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
Answer 11
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
Answer 12
-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
Question 13
Thrombocytopenia
Answer 13
-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