_____ is a qualitative platelet disorder due to a genetic GPIIb/IIIa deficiency
RBCs stored in _____ can be kept until 35 days
In TTP, large, uncleaved vWF multimers lead to increased platelet _____ with consequent microthrombi formation
In multiple myeloma, neoplastic plasma cells produce _____ and MIP1, which stimulates osteoclast maturation that will lead to bone resorption
Vitamin K deficiency presents with _____ PT and increased (in severe cases) PTT
_____ leukemia/lymphoma may present with lytic (punched-out) bone lesions and hypercalcemia
_____ is a neoplastic proliferation of mature myeloid cells, especially megakaryocytes
_____ lymphoma is characterized by painless "waxing and waning" lymphadenopathy
_____ may be confirmed via flow cytometry, which detects a lack of CD-55 and CD-59
_____ macrocytic anemia occurs when DNA synthesis is unimpaired (impaired or unimpaired)
Anemias: Classification and Approach
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Hemolytic Anemias
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Myeloproliferative Neoplasms
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Myelodysplastic Syndromes
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Acute Leukemias
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Chronic Leukemias
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Lymphomas and Lymphoid Neoplasms
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Plasma Cell Disorders
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Bleeding Disorders
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Thrombotic Disorders
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