Exam 25: Disorders of Primary Hemostasis: Quantitative and Qualitative Platelet Disorders and Vascular 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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The antibody present in the patient's serum in posttransfusion purpura is directed against the platelet antigen __________.
(Multiple Choice)
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The laboratory tests used in the diagnosis of vWD include all of the following except:
(Multiple Choice)
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The average platelet count ranges from __________ of whole blood.
(Multiple Choice)
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Which qualitative congenital platelet disorder is characterized by a prolonged bleeding time; unusually large platelets; and decrease in platelet surface glycoprotein Ib, glycoprotein V, and glycoprotein IX resulting in decreased platelet adhesion?
(Multiple Choice)
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Endothelial cells and __________ are known to synthesize vWF.
(Multiple Choice)
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Decreased platelet production may be associated with congenital or acquired disorders that affect the bone marrow, resulting in __________.
(Multiple Choice)
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A deficiency of ___________________ results in gray platelet syndrome:
(Multiple Choice)
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Which purpose would a splenectomy serve in treatment of acute ITP?
(Multiple Choice)
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How is May-Hegglin anomaly distinguished from Bernard-Soulier syndrome?
(Multiple Choice)
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The prolonged bleeding time and abnormal platelet adhesion seen in vWD is due to the lack of __________.
(Multiple Choice)
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Laboratory findings in TTP include all of the following except:
(Multiple Choice)
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All of the following are established criteria for the diagnosis of Bernard-Soulier syndrome except:
(Multiple Choice)
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What is the treatment of choice to convert the hemostatic defect in uremia?
(Multiple Choice)
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The congenital disorders of platelet function include defects in all of the following except:
(Multiple Choice)
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In patients with alcoholic cirrhosis, thrombocytopenia and platelet abnormalities may result from the direct toxic effect of alcohol on bone marrow __________, leading to an ineffective thrombopoiesis.
(Multiple Choice)
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The etiology of Glanzmann's thrombasthenia results from the inability of __________ to bind to platelet surface membranes, which would normally result in aggregation.
(Multiple Choice)
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__________ results from immunization of the mother by fetal platelet antigen and placental transfer of maternal antibody.
(Multiple Choice)
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