Exam 22: Multiple Myeloma and Related Plasma Cell Disorders
Exam 1: Morphology of Human Blood and Marrow Cells: Hematopoiesis28 Questions
Exam 2: Bone Marrow29 Questions
Exam 3: The Red Blood Cell: Structure and Function64 Questions
Exam 4: Anemia: Diagnosis and Clinical Considerations33 Questions
Exam 5: Evaluation of Red Blood Cell Morphology and Introduction to Platelet and White Blood Cell Morphology29 Questions
Exam 6: Iron Metabolism and Hypochromic Anemias31 Questions
Exam 7: Megaloblastic Anemias29 Questions
Exam 8: Aplastic Anemia Including Pure Red Cell Aplasia and Congenital Dyserythropoietic Anemia and Paroxysmal Nocturnal Hemoglobinuria48 Questions
Exam 9: Introduction to Hemolytic Anemias: Intracorpuscular Defects: I Hereditary Defects of the Red Cell Membrane36 Questions
Exam 10: Hemolytic Anemias: Intracorpuscular Defects: II Hereditary Enzyme Deficiencies20 Questions
Exam 11: Hemolytic Anemias: Intracorpuscular Defects: III the Hemoglobinopathies75 Questions
Exam 12: Hemolytic Anemias: Intracorpuscular Defects: Iv Thalassemia30 Questions
Exam 13: Hemolytic Anemias: Extracorpuscular Defects51 Questions
Exam 14: Hypoproliferative Anemia: Anemia Associated With Systemic Diseases32 Questions
Exam 15: Cell Biology, Disorders of Neutrophils, Infectious Mononucleosis, and Reactive Lymphocytosis44 Questions
Exam 16: Introduction to Leukemia and the Acute Leukemias74 Questions
Exam 17: Chronic Myeloproliferative Disorders I: Chronic Myelogenous Leukemia24 Questions
Exam 18: Chronic Myeloproliferative Disorders Ii: Polycythemia Vera, Essential Thrombocythemia, and Idiopathic Myelofibrosis56 Questions
Exam 19: Myelodysplastic Syndromes28 Questions
Exam 20: Chronic Lymphocytic Leukemia and Related Lymphoproliferative Disorders29 Questions
Exam 21: The Lymphomas41 Questions
Exam 22: Multiple Myeloma and Related Plasma Cell Disorders45 Questions
Exam 23: Lipid Lysosomal Storage Diseases and Histiocytosis37 Questions
Exam 24: Introduction to Hemostasis113 Questions
Exam 25: Disorders of Primary Hemostasis: Quantitative and Qualitative Platelet Disorders and Vascular Disorders62 Questions
Exam 26: Disorders of Plasma Clotting Factors48 Questions
Exam 27: Interaction of the Fibrinolytic, Coagulation, and Kinin Systems; Disseminated Intravascular Coagulation; and Related Pathology44 Questions
Exam 28: Introduction to Thrombosis and Anticoagulant Therapy66 Questions
Exam 29: Quality Control in the Hematology Laboratory22 Questions
Exam 30: Body Fluid Examination: the Qualitative, Quantitative, and Morphologic Analysis of Serous, Cerebrospinal, and Synovial Fluids36 Questions
Exam 31: Hematology Methods114 Questions
Exam 32: Principles of Automated Differential Analysis25 Questions
Exam 33: Coagulation Procedures61 Questions
Exam 34: Applications of Flow Cytometry to Hematology and Hemostasis20 Questions
Exam 35: Molecular Diagnostic Techniques in Hematopathology34 Questions
Exam 36: Special Stainscytochemistry38 Questions
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What is the benefit of plasmapheresis used for treating patients with Waldenström's macroglobulinemia?
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(Multiple Choice)
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A
Myeloma cells may diffusely infiltrate organs such as the __________ resulting in enlargement and dysfunction.
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(Multiple Choice)
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D
Myeloma patients treated with alkylating agents have a significant risk of developing treatment-related __________.
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(Multiple Choice)
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A
Which multiple myeloma manifestation describes the formation of abnormal proteins in organ systems due to deposition of immunoglobulin light chains leading to kidney and renal dysfunction?
(Multiple Choice)
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Serum protein electrophoresis (SPEP) demonstrates the absence of a gamma peak. This finding is consistent with which plasma cell disorder?
(Multiple Choice)
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Urine immunoelectrophoresis is used to distinguish between __________ and __________ light chains in urine.
(Multiple Choice)
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When evaluating a plasma cell disorder, which immunologic technique is capable of quantitating a monoclonal immunoglobulin?
(Multiple Choice)
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In multiple myeloma, a plasma cell will sometimes contain clumps of aggregated immunoglobulin that stain red with Wright-Giemsa stain. These aggregates are referred to as:
(Multiple Choice)
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Neurologic manifestations such as blurred vision, headaches, and episodes of consfusion occur in patients with Waldenström's macroglobulinemia due to __________.
(Multiple Choice)
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Which of the following immunoglobulins are associated with heavy chain disease?
(Multiple Choice)
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Which light chain protein is characteristically present in multiple myeloma?
(Multiple Choice)
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Bacterial infection is the most common cause of death in multiple myeloma patients due to __________.
(Multiple Choice)
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Extramedullary infiltration of plasmacytoid lymphs in Waldenström's macroglobulinemia occurs in the __________.
(Multiple Choice)
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A __________ is a protein that precipitates on exposure to cold, causing such symptoms as Raynaud's phenomenon and thrombosis of small arteries in Waldenström's macroglobulinemia.
(Multiple Choice)
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Which class of immunoglobulin has the largest molecular weight?
(Multiple Choice)
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What is the cause of decreased production of formed elements in the marrow (red cells, white cells, platelets) seen in patients with multiple myeloma?
(Multiple Choice)
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Immune globulins (antibodies) are proteins produced by __________.
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