deficiency in erythrocytes or hemoglobin
-most common type is iron deficiency anemia; causes by a lack of iron, which is required (iron is required) for hemoglobin production
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chronic lymphocytic leukemia (CLL)
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abnormal numbers of relatively mature lymphocytes predominate in the marrow, lymph nodes, and spleen
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leukemia
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cancer of white blood cells
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aplastic anemia
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failure of blood cell production in the bone marrow
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pancytopenia
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occurs when stem cells fail to produce leukocytes, platelets, and erythrocytes
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polycythemia vera
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general increase in red blood cells
-blood consistency is thick
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autologous bone marrow transplantation (ABMT)
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which the patient serves as his or her own donor for stem cells, may lead to a prolonged remission
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basophila
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an increase happens in certain types of leukemia
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remission
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effective treatment canceled the disappearances f signs and symptoms of disease
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actue myelogenous (myelocytic) leukemia (AML)
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immature granulocytes(myeloblasts) predominate.
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acute lymphocytic leukemia (ALL)
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Immature lymphocytes (lymphoblasts) predominate. This form is seen most often in children and adolescents; onset is sudden
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chronic myelogenous (myelocytic) leukemia (CML)
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Both mature and immature granulocytes are present in large numbers in the marrow and bloodstream.
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mononucleosis
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infectious disease marked by increased numbers of leukocytes and enlarged cervical lymph nodes
-transmitted by EPstein-Bear virus(EBV); direct oral contact salivary rechange
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ecchymoses
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larger blue or purplish patches on the skin (bruises)
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eosinophilia
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increase in eosinophils in granulocytes, seen in allergic conditions and parasitic infectious
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why would there be an increase in neutrophils
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it may occur in responsible to infection or information of any type.
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palliative
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relieving symptoms, but not curing the disease
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hemolytic anemia
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reduction in red cells due to excessive destruction
-removal of spleen improves this anemia
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thalassemia
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Inherited defect in the ability to produce hemoglobin, usually seen in persons of Mediterranean background.
- leads to hypochromic anemia
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sickle cell anemia
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hereditary condition characterized by abnormal sickle shape of erythrocytes and by hemolysis
-caused by abnormal type of hemoglobin (s)
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granulocytosis
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abnormal increase in granulocytes in the blood
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purpura
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multiple pinpoint hemorrhages and accumulation of blood under the skin
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hemophilia
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excessive bleeding caused by hereditary lack of blood clotting factors necessary for blood clotting(factor 8 or 11)
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blood dyscrasia (disease)
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any abnormal or pathologic condition of the blood
-> diseases of: RBC, WBC, blood clotting and bone marrow
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multiple myeloma
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malignant neoplasm of bone marrow
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hemochromatosis
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excess iron deposits throughout the body
-skin pigmentation, diabetes, hepatomegaly and cardiac failure may occur
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petechia
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tiny purple or red flat spots appearing on the skin as a result of hemorrhages;small bruise
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autoimmune thrombocytopenic purpura
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condition in which a patient makes an antibody that destroys platelets
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pernicious anemia
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lack of mature erythrocytes caused by inability to absorb vitamin B12 into the body/bloodstream
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relapse
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occurs when disease symptoms and signs reappear, necessitating further treatment