Exam 23: Acute Myeloid Leukemias
Exam 1: Introduction34 Questions
Exam 2: Cellular Homeostasis40 Questions
Exam 3: Hematopoiesis35 Questions
Exam 4: Structure and Function of Hematopoietic Organs34 Questions
Exam 5: The Erythrocyte33 Questions
Exam 6: Hemoglobin35 Questions
Exam 7: The Leukocyte37 Questions
Exam 8: Introduction to Anemia35 Questions
Exam 9: Anemias of Disordered Iron Metabolism and Heme Synthesis36 Questions
Exam 10: Hemoglobinopaties: Qualitative Defects33 Questions
Exam 11: Thalassemia32 Questions
Exam 12: Megaloblastic and Nonmegaloblastic Macrocytic Anemias67 Questions
Exam 13: Introduction to Hemolytic Anemia32 Questions
Exam 14: Hemolytic Anemia: Membrane Defects36 Questions
Exam 15: Hemolytic Anemia: Enzyme Deficiencies35 Questions
Exam 16: Hemolytic Anemia: Immune Anemias30 Questions
Exam 17: Hemolytic Anemia: Nonimmune Defects32 Questions
Exam 18: Nonmalignant Granulocyte and Monocyte Disorders23 Questions
Exam 19: Nonmalignant Lymphocyte Disorders32 Questions
Exam 20: Introduction to Hematopoietic Neoplasms34 Questions
Exam 21: Myeloproliferative Disorders41 Questions
Exam 22: Myelodysplastic Syndromes33 Questions
Exam 23: Acute Myeloid Leukemias35 Questions
Exam 24: Acute Lymphoblastic Leukemias35 Questions
Exam 25: Lymphoid Malignancies: Chronic Lymphoid Leukemias, Lymphomas, and Plasma Cell Neoplasms34 Questions
Exam 26: Hematopoietic Stem Cell Transplantation43 Questions
Exam 27: Morphologic Analysis of Body Fluids in the Hematology Laboratory39 Questions
Exam 28: Primary Hemostasis34 Questions
Exam 29: Secondary Hemostasis and Fibrinolysis33 Questions
Exam 30: Disorders of Primary Hemostasis33 Questions
Exam 31: Disorders of Secondary Hemostasis35 Questions
Exam 32: Thrombophilia35 Questions
Exam 33: Hematology Procedures and Hemostasis46 Questions
Exam 34: Bone Marrow Examination34 Questions
Exam 35: Automation in Hematology and Hemostasis39 Questions
Exam 36: Flow Cytometry35 Questions
Exam 37: Chromosome Analysis of Hematopoietic and Lymphoid Disorders35 Questions
Exam 38: Molecular Analysis of Hematologic Diseases15 Questions
Exam 39: Laboratory Testing in Coagulation39 Questions
Exam 40: Quality Assessment in the Hematology Laboratory41 Questions
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A technologist is reviewing a blood smear of an AML patient.She notices single azurophilic needle-like inclusions in the cytoplasm of many of the circulating blasts.What is the most probable identification of the inclusion?
(Multiple Choice)
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A technologist is reviewing a peripheral blood smear of a 10-year-old patient.She notices that 35% blasts are present on the patient's smear.What can you conclude from these findings?
(Multiple Choice)
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Which of the following markers are positive for monoblasts?
(Multiple Choice)
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A PAS stain is ordered on a leukemic patient.The test is performed, and the technologist confirms that the PAS stain is positive with coarse granularity.Based on these findings, from what is the patient most likely suffering?
(Multiple Choice)
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List the common cytochemical stains used in the detection of AML, and predict their results in AML.
(Essay)
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Which of the following cell markers will differentiate AML from ALL?
(Multiple Choice)
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Bone marrow review on a 15-year-old girl with acute leukemia revealed many blasts with the following characteristics: high N:C ratio, prominent nucleoli, open chromatin pattern, and basophilic cytoplasm.Cytochemical staining revealed negative reactivity with MPO and SBB.Nonspecific esterase was positive.No cytogenetic abnormalities were detected.What is the most likely lineage of the blast cells in question?
(Multiple Choice)
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Use this case to answer the following questions:
A 45-year-old female sees her physician because of unexplained bruising on her upper torso. The physician takes a history, and nothing remarkable is noted. Physical examination reveals a palpable liver and spleen. CBC results reveal a platelet count of 5,000/µL and WBC count of 12,000/µL with 80% blasts and 15% promyelocytes present. Additional CBC findings include: Hgb: 8.7 g/dL and Hct: 25% normal indices.
Bone marrow findings: hypercellular marrow with 47% myeloblasts present. Nucleated erythroblasts: 22%; promyelocytes: 28%; megakaryopoiesis appears normal.
Cytogenetic analysis: t (15, 17) present.
-Flow cytometry has also been ordered on this patient.Which of the following markers will stain positive in this case?
(Multiple Choice)
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The distinction between the FAB classification and the WHO classification is based on which of the following?
(Multiple Choice)
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What is the typical erythrocyte morphologic picture in patients with AML?
(Multiple Choice)
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A technologist is reviewing a CBC on a new admission.The patient has a WBC count of 5 x 103/µL with 32% blasts present.From what is the patient most likely suffering?
(Multiple Choice)
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According to the WHO classification, what must be true to differentiate myelodysplastic syndromes from acute leukemia? In acute leukemia:
(Multiple Choice)
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An APL patient has been undergoing ATRA therapy for the last 5 weeks.A repeat bone marrow and cytogenetic analysis are performed at the end of the treatment cycle.Bone marrow shows no evidence of leukemic cells, and cytogenetic anomalies were not detected.Based on this information, what is the status of the patient?
(Multiple Choice)
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