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Blood test

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Question
Answer
Anemia   Condition marked by reduction in erythrocyte count or hgb concentration.  
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Blood Dyscrasia   Morbid blood condtion  
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Ecchymosis   bruising  
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Erythrocytosis   Abnormal increase in RCS's  
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Erythrocytopenia   Deacrease in RBC's  
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Leukocytosis   Abnormal increase in WBC  
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Leukocytopenia   Decrease in WBC  
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Petechiae   Small pinpoint hemorrhagic spots on the skin.  
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Pancytopenia   Abnormal Reduction of all blood cells  
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Polycythemia   Increase in cell mass and hemoglobin concentration  
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Proliferation   Increase in production of cells  
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Perisplenitis   Inflammation of the spleen and surrounding structures  
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Rouleaux formation   RBC's that resemble stacked coins  
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Thrombocytosis   Increased amount of platelets in the blood  
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Thrombocytopenia   Decreased amount of platelets in the blood  
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Hemolysis   Destruction of RBS's  
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Hemangioma   Benign tumor of blood vessels  
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Hematoma   Blood tumor  
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Normocytic   Normal size in RBC  
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Macrocytosis   Abnormally large RBC's  
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Microcytosis   Abnormally small RBC's  
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Normochromic   Normal RBC color  
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Hypochromic   RBC's are pale in color  
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Hyperchromic   RBC's have to much color  
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Anisocytosis   Abnormal variation of RBC size  
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Poikilocytosis   Abnormal RBC shapes  
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Bactermia   Bacteria in the blood  
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Speticemia   Blood poisoning due to pathogens  
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Viremia   Virus in the blood  
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Iron defciency anemia   Caused by impaired iron intake or excessive blood loss.  
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Pernicious anemia   Anemia which is caused from a lack on the intrinsic factor. Vital for B12 absorption.  
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Folic acid deficiency anemia   inadequate folic acid intake  
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Vitamin K deficiency   Lack of Vit K in the intestine after antibiotic treatment  
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Thalassemia   Hereditary condtion marked by defective production of Hgb.  
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Von Willebrand disease   Hereditary bleeding disorder related to deficient or abnormal Willibrand factor  
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Hemophilia A   Hereditary bleeding disorder from a deficiency or malfunction of clotting factor VIII  
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Hemophilia B   Hereditary bleeding disorder from a deficiency of factor IX  
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Thrombocytopenia   Hemorrhagic disorder caused by a deficiency in circulating platelets. With sudden onset of petechiae or ecchymoses  
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idiopathic thrombocytopenic purpura   Platelet disorder caused by antibodies directed against platelets  
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Drug induced thrombocytopenia   Side effect of many medications  
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thrombotic thrombocytopenic purpura   Causes platelet aggregation and inappropriate clor formation bleeding  
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Polycythemia   Myeloproliferative malignant disorder marks by an increase in RBC HgB hematocrit and blood viscosity  
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Leukemia   Malignant proliferation of WBC precursors in the bone marrow and the subsequent accumulation in the blood/body tissues.  
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Multiple myeloma   Neoplasm of bone marrow plasma cells produce lesions throughout the skeleton and internal organs  
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Aplastic anemia   Anemia brought on by failure of bone marrow to adequately produce blood cells.  
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Hemolytic anemia   Increased fragility and destruction of RBC's with a increase of reticulocytes being released into the blood.  
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Erythroblastosis fetalis   Hemolytic anemia that results from antibodies in an RH - mother and a Rh + fetus.  
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Plasma   Water portion of blood 55% of blood volume and 92% water.  
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Serum   Liquid portion minus the clotting factor  
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Formed Elements   Cellular portion of blood 45%  
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Reticulocytes   Immature RBC  
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Erythropoises   Formation of RBC's  
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Hemopoiesis   Formation of blood  
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Agglutination   Clumping together of RBC. Transfusion rxn.  
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Phagocytosis   Ingestion of dead cells, CA cells, and bacteria  
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Thrombocyte   Platelet  
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Erythrocyte   RBC  
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Leukocyte   WBC  
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Albumin   Plasma protein that maintains the water balance in the blood  
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Phagocyte   Cells that preforms phagocytosis  
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Neutropenia   Decreased neutrophil count  
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Fibrinogen   Essential component of blood clotting process  
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Coagulopathy   Any disease that impairs blood clotting.  
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