Exam 26: Acute Myeloid Leukemias
Exam 1: Introduction32 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 Platelet18 Questions
Exam 10: The Complete Blood Count and Peripheral Blood Smear Evaluation40 Questions
Exam 11: Introduction to Anemia34 Questions
Exam 12: Anemias of Disordered Iron Metabolism and Heme Synthesis40 Questions
Exam 13: Hemoglobinopathies: Qualitative Defects33 Questions
Exam 14: Thalassemia32 Questions
Exam 15: Megaloblastic and Nonmegaloblastic Macrocytic Anemias33 Questions
Exam 16: Hypoproliferative Anemias31 Questions
Exam 17: Hemolytic Anemia: Membrane Defects36 Questions
Exam 18: Hemolytic Anemia: Enzyme Deficiencies36 Questions
Exam 19: Hemolytic Anemia: Immune Anemias32 Questions
Exam 20: Hemolytic Anemia: Nonimmune Defects30 Questions
Exam 21: Nonmalignant Disorders of Leukocytes: Granulocytes and Monocytes36 Questions
Exam 22: Nonmalignant Lymphocyte Disorders35 Questions
Exam 23: Introduction to Hematopoietic Neoplasms33 Questions
Exam 24: Myeloproliferative Neoplasms43 Questions
Exam 25: Myelodysplastic Syndromes34 Questions
Exam 26: Acute Myeloid Leukemias36 Questions
Exam 27: Precursor Lymphoid Neoplasms33 Questions
Exam 28: Mature Lymphoid Neoplasms41 Questions
Exam 29: Hematopoietic Stem Cell Transplantation41 Questions
Exam 30: Morphologic Analysis of Body Fluids in the Hematology42 Questions
Exam 31: Primary Hemostasis32 Questions
Exam 32: Secondary Hemostasis and Fibrinolysis35 Questions
Exam 33: Disorders of Primary Hemostasis36 Questions
Exam 34: Disorders of Secondary Hemostasis31 Questions
Exam 35: Thrombophilia38 Questions
Exam 36: Hemostasis: Laboratory Testing and Instrumentation50 Questions
Exam 37: Hematology Procedures44 Questions
Exam 38: Bone Marrow Examination33 Questions
Exam 39: Automation in Hematology27 Questions
Exam 40: Flow Cytometry33 Questions
Exam 41: Chromosome Analysis of Hematopoietic and Lymphoid Disorders34 Questions
Exam 42: Molecular Analysis of Hematologic Diseases17 Questions
Exam 43: Quality Assessment in the Hematology Laboratory29 Questions
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Which of the following laboratory findings would be most consistent with this clinical picture?
(Multiple Choice)
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A bone marrow sample is sent to the lab for cytochemical staining. MPO, SBB, and nonspecific esterase (NSE) have been ordered. Staining results come back as follows: MPO: positive SBB: positive NSE: positive
Based on these findings, what lineage(s) is(are) most likely affected?
(Multiple Choice)
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A 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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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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Immunophenotyping is ordered on a bone marrow aspirate from a newly diagnosed patient with leukemic blasts. What panel of markers could differentiate AML from ALL?
(Multiple Choice)
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A laboratory professional reviewed the CBC of a patient who had a WBC count of 5 × 103/μL with 32% blasts present. Follow up testing with cytogenetics revealed t(15;17)(q22;q12). Which of the following is a likely diagnosis for the patient?
(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 is 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 patient's status?
(Multiple Choice)
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A laboratory professional notes single azurophilic needlelike inclusions in the cytoplasm of many of the circulating blasts while reviewing a blood smear of an AML patient. What is the most probable identification of the inclusion?
(Multiple Choice)
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Predict the typical platelet concentration of a patient with AML.
(Multiple Choice)
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An acute leukemia patient presents with blast morphology that is of neutrophil lineage with Auer rods and pseudo-Pelger-Huët nuclei, myeloperoxidase, and Sudan Black B. Cytogenetic analysis reveals a t(8;21)(q22;q22) translocation in the majority of the blasts. Which classification of AML best fits this morphology, immunophenotyping, and cytochemistry?
(Multiple Choice)
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Patients with acute myelomonocytic leukemia are at higher risk of infection compared with individuals with acute myelocytic leukemia with differentiation. Explain why there is a higher risk of infection in patients diagnosed with acute myelomonocytic leukemia.
(Essay)
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Which acute leukemia is characterized by a blast population with both myeloid and monocytic markers on the same cell?
(Multiple Choice)
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A patient presents with a morphological smear examination revealing >20% blasts with prominent granules and Auer rods, MPO, and SBB positive. A 25% monocyte count was seen in the peripheral smear. There were no recurrent cytogenetic abnormalities observed. Under which classification of acute leukemia, not otherwise specific, does this diagnosis fall?
(Multiple Choice)
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