Exam 24: Myeloproliferative Neoplasms
Exam 1: Introduction30 Questions
Exam 2: Cellular Homeostasis40 Questions
Exam 3: Structure and Function of Hematopoietic Organs35 Questions
Exam 4: Hematopoiesis35 Questions
Exam 5: The Erythrocyte37 Questions
Exam 6: Hemoglobin40 Questions
Exam 7: Granulocytes and Monocytes30 Questions
Exam 8: Lymphocytes25 Questions
Exam 9: The Platelet16 Questions
Exam 10: The Complete Blood Count and Peripheral Blood Smear Evaluation35 Questions
Exam 11: Introduction to Anemia35 Questions
Exam 12: Anemias of Disordered Iron Metabolism and Heme Synthesis36 Questions
Exam 13: Hemoglobinopathies: Qualitative Defects33 Questions
Exam 14: Thalassemia32 Questions
Exam 15: Megaloblastic and Nonmegaloblastic Macrocytic Anemias34 Questions
Exam 16: Hypoproliferative Anemias32 Questions
Exam 17: Hemolytic Anemia: Membrane Defects36 Questions
Exam 18: Hemolytic Anemia: Enzyme Deficiencies36 Questions
Exam 19: Hemolytic Anemia: Immune Anemias30 Questions
Exam 20: Hemolytic Anemia: Nonimmune Defects30 Questions
Exam 21: Nonmalignant Disorders of Leukocytes: Granulocytes and Monocytes35 Questions
Exam 22: Nonmalignant Lymphocyte Disorders32 Questions
Exam 23: Introduction to Hematopoietic Neoplasms34 Questions
Exam 24: Myeloproliferative Neoplasms44 Questions
Exam 25: Myelodysplastic Syndromes34 Questions
Exam 26: Acute Myeloid Leukemias35 Questions
Exam 27: Precursor Lymphoid Neoplasms34 Questions
Exam 28: Mature Lymphoid Neoplasms39 Questions
Exam 29: Hematopoietic Stem Cell Transplantation41 Questions
Exam 30: Morphologic Analysis of Body Fluids in the Hematology Laboratory39 Questions
Exam 31: Primary Hemostasis35 Questions
Exam 32: Secondary Hemostasis and Fibrinolysis33 Questions
Exam 33: Disorders of Primary Hemostasis35 Questions
Exam 34: Disorders of Secondary Hemostasis34 Questions
Exam 35: Thrombophilia34 Questions
Exam 36: Hemostasis: Laboratory Testing and Instrumentation41 Questions
Exam 37: Hematology Procedures46 Questions
Exam 38: Bone Marrow Examination34 Questions
Exam 39: Automation in Hematology38 Questions
Exam 40: Flow Cytometry34 Questions
Exam 41: Chromosome Analysis of Hematopoietic and Lymphoid Disorders35 Questions
Exam 42: Molecular Analysis of Hematologic Diseases18 Questions
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Which of the following test results is most consistent with a diagnosis of PMF?
Free
(Multiple Choice)
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Correct Answer:
C
Which of the following are criteria for systemic mastocytosis?
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(Multiple Choice)
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Correct Answer:
D
The myeloproliferative disorder best described by increased leukocytes,immature granulocytes,and decreased LAP with the Philadelphia chromosome present is which of the following?
Free
(Multiple Choice)
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Correct Answer:
B
A known CML patient's blood is received in the lab for a routine CBC.The laboraty professional counts 55% blasts in the smear.The most likely reason for this occurrence is that the patient is in:
(Multiple Choice)
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A patient's CBC revealed marked leukocytosis with an increased number of immature granulocytes.A few promyelocytes and blasts were seen.There were also an increased number of eosinophils and basophils with rare immature forms.The hemoglobin and hematocrit were normal,but platelets were slightly decreased.Which disorder is associated with these findings?
(Multiple Choice)
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Which of the following tests would help differentiate primary polycythemia from secondary polycythemia?
(Multiple Choice)
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Which of the following would differentiate a myeloproliferative disorder from a myelodysplastic disorder?
(Multiple Choice)
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Which is a characteristic of ET that would help distinguish it from reactive thrombocytosis?
(Multiple Choice)
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A 45-year-old male patient presents to his physician with a palpable spleen.A CBC reveals an absolute eosinophil count of 2.5 × 10⁹/L.After six weeks,the patient's CBC indicates an absolute eosinophil count of 2.9 × 10⁹/L.Which of the following is a likely diagnosis for this patient?
(Multiple Choice)
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A physician strongly suspects CML in a patient and has already ordered a bone marrow differential and cytogenetic analysis for the Philadelphia chromosome.What other test would help confirm the CML picture for this patient?
(Multiple Choice)
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The key factor to distinguish relative and absolute polycythemia is that a relative polycythemia is caused by:
(Multiple Choice)
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The Philadelphia chromosome results from the fusion of which of the following?
(Multiple Choice)
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Contrast primary polycythemia and secondary polycythemia based on pathophysiology.
(Essay)
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A patient's laboratory results indicate a markedly increased hemoglobin,hematocrit,and red blood cell count.White blood cells and platelets are also slightly increased.The erythropoietin level is decreased.Which is most likely :
(Multiple Choice)
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A patient presents with a moderate leukoerythroblastic anemia,striking anisocytosis,and poikilocytosis.The anemia is normocytic,normochromic.Large platelets are noted.Dacryocytes,elliptocytes,and ovalocytes are present.Basophilic stippling is present.What disease is associated with these findings?
(Multiple Choice)
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The characteristic poikilocyte often seen in the peripheral blood of patients with PMF that indicates extramedullary hematopoiesis is:
(Multiple Choice)
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