chapter 13 pathology - blood diseases

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24 Terms

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Multiple pinpoint hemorrhages and accumulation of blood under the skin
Purpura
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General increase in red blood cells (erythremia)
Polycythemia Vera
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Excess iron deposits throughout the body
Hemochromatosis
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Hereditary condition characterized by abnormal crescent shape of erythrocytes and by hemolysis
Sickle cell anemia
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Inherited defect in the ability to produce hemoglobin, usually seen in persons of Mediterranean background
Thalassemia
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Infectious disease marked by increased numbers of leukocytes and enlarged cervical lymph nodes
Mononucleosis
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Reduction in red cells due to excessive destruction
Hemolytic anemia
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Failure of blood cell production due to absence of formation of bone marrow cells
Aplastic anemia
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Excessive bleeding caused by hereditary lack of factor VIII or factor IX necessary for blood clotting
Hemophilia
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Lack of mature erythrocytes caused by inability to absorb vitamin B12 into the body
Pernicious anemia
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Abnormal numbers of relatively mature lymphocytes predominate in the bone marrow, lymph nodes, and spleen (Cll)
chronic lymphocytic leukemia
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Immature granulocytes predominate in the bone marrow (AML)
Acute myelogenous leukemia (myelocytic)
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Both mature and Immature granulocytes are present in the bone marrow and blood stream (CML)
Chronic myelogenous leukemia (myelocytic)
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Immature lymphocytes predominate in the bone marrow and lymph nodes
Acute lymphocytic leukemia
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Tiny purple or red flat spots on the skin as a result of hemorrhages
Petechiae
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Causative agent in mononucleosis
Epstein- Barr Virus
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Large blue or purplish patches in the skin (bruises)
Ecchymoses
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Sideropenia is the cause of this condition
Iron deficiency anemia
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Any disease of the blood or bone marrow
Dyscrasia
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Disappearance of signs and symptoms of disease
Remission
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Relieving, but not curing disease
Palliative
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Disease symptoms and signs reappear
Relapse
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Malignant neoplasm of bone marrow
Multiple myeloma
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Increase in numbers of granulocytes associated with allergic conditions
Eosinophilia