ASCP Hematology
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Wright's stain, Schuffner's dot, parasites with irregular "spread-out" trophozoites | Plasmodium vivax
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RBC erroneously increased | decreased MCH
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glucocerebrosidase deficiency | Gaucher's disease
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disease most closely associated with cytoplasmic granule fusion. | Chediak-Higashi syndrome
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disease most closely associated with mucopolysaccharidosis. | Alder-Reilly anomaly
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characteristic morphologic feature in folic acid deficiency | macrocytosis
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differentiate leukomoid reactions vs chronic granulocytic leukemias | leukocyte alkaline phosphatase
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Terminal deoxynucleotidyl transferase (TdT) is marker found on: | lymphoblasts
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leukocyte alkaline phosphatase activity is increased in: | leukemoid reaction
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ALL, the acid phosphatase stain is usually positive for: | T cell ALL
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PB monocyte is an intermediate stage for | histiocyte
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characteristic of Auer rods | lysosome and acid phosphate positive
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precursors of tissue macrophages | monocytes
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stain for evaluation of BM | Romanowsky and Prussian blue stain
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atypical lymphocyte seen in the perismear of patient with IM. | T lymphocytes
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platelet aggregation will occur with the end production of: | thromboxane A2
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megaloblastic asynchronous development in the BM indicate | impaired synthesis of DNA
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type of leukemia seen most commonly as a terminal event in multiple myeloma | acute myelogenous leukemia
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occur in the presence of cold agglutinin | increased MCV and decreased RBC
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EDTA, RT at 6-24hrs | increased hematocrit and MCV
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substrate used to detect specific esterase | chloroacetate
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characteristic of Factor XII deficiency | negative bleeding history
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most closely associated with chronic myelomonocytic leukemia | lysozymuria
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most closely associated with erythroleukemia | ringed sideroblasts
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Vitamin-K dependent | Factor VII
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mean value of a reticulocyte on cord blood | 5 %
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hypercellular marrow with an M:E of 6:1 | granulocytic hyperplasia
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B cell origin | Waldenstroms macroglobulinemia
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most closely associated with megaloblastic anemia | neutropenia and thrombocytopenia
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most useful in differentiating hemophilia A and B. | mixing studies
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most closely associated with idiopathic hemochromatosis | iron overload in tissue
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seen most often in thalassemia | target cells
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use to stain neutral fats, phospholipids, and sterols | Sudan Black B
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