Exam 19: Myelodysplastic Syndromes
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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Which type of MDS demonstrates a mild decreased white blood cell (WBC) count (3.9 10/L), increased erythropoiesis and normal numbers of blast cells in the marrow, and <15% sideroblasts?
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(Multiple Choice)
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Correct Answer:
B
The fundamental characteristic of MDS is:
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(Multiple Choice)
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Correct Answer:
B
The French-American-British (FAB) classification system separates the myelodysplastic syndromes into __________ different types.
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(Multiple Choice)
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Correct Answer:
C
A type III sideroblast in dyserythropoiesis is demonstrated by:
(Multiple Choice)
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Which of the following represents the "cornerstone" of myelodysplastic-syndrome treatment?
(Multiple Choice)
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What is the purpose of transfusing granulocytes to a patient with RA?
(Multiple Choice)
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Which factor(s) differentiate(s) RARS (refractory anemia with ringed sideroblasts) from refractory anemia?
(Multiple Choice)
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In calculating the percentage of myeloblasts in the bone marrow, the following data are given. Erythroid nuclear precursors (E) = 65%, myeloblasts = 14%, other cells = 21%. Based on these numbers, what is the percentage of myeloblasts by the FAB classification?
(Multiple Choice)
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Which of the following is most likely to affect prognosis in MDS?
(Multiple Choice)
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What characterizes the cytogenetic analysis of patients with MDS?
(Multiple Choice)
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The most promising course of therapy for MDS is __________.
(Multiple Choice)
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Which of the following is the most significant prognostic indicator in MDS?
(Multiple Choice)
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RAEB contains a maximum of __________ blasts in the bone marrow.
(Multiple Choice)
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What specific features are characteristic of dysmegakaryocytopoiesis morphology in MDS (myelodysplastic syndrome)?
(Multiple Choice)
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Which of the following agents may lead to secondary myelodysplastic syndrome (sMDS)?
(Multiple Choice)
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The most common and consistent nonrandom chromosomal aberration in the MDS, refractory anemia is deletion of the long arm of __________.
(Multiple Choice)
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