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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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.
-What is the most likely diagnosis?
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(Multiple Choice)
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Correct Answer:
C
Use the case below to answer the following questions:
A 57-year-old male is admitted with suspicion of AML. Preliminary CBC results show a high WBC count with 47% blasts present. Cytochemical staining shows negative reactions with MPO, SBB, and NSE. Platelet peroxidase staining was positive. Immunophenotyping was also ordered.
-Predict the results of the immunophenotyping panel based on the information already given.
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(Multiple Choice)
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Correct Answer:
B
A patient presents with 25% blasts (nonerythroid), 34% monocytic cells, and 31% granulocytic cells in the bone marrow.The peripheral blood smear has 10% monocytes.The alpha-naphthyl esterase and chloroacete esterase are positive.What is the probable diagnosis based on these findings?
Free
(Multiple Choice)
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Correct Answer:
C
A patient presents with acute leukemia, with blasts identified by a positive CD34, CD13, and CD33.Less than 3% of the blasts stain positive for MPO and SBB.Which category of AML is the most likely diagnosis for this patient?
(Multiple Choice)
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The FAB classification nomenclature for acute leukemia also appears under which WHO classification group?
(Multiple Choice)
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A patient presents with a morphological smear examination revealing greater than 20% blasts with prominent granules and ++ Auer rods, MPO, and Sudan Black 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 categorized, does this picture fall?
(Multiple Choice)
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The presence of which of the following findings with a blast of unknown lineage confirms that the lineage is myeloid?
(Multiple Choice)
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Use the case below to answer the following questions:
A 57-year-old male is admitted with suspicion of AML. Preliminary CBC results show a high WBC count with 47% blasts present. Cytochemical staining shows negative reactions with MPO, SBB, and NSE. Platelet peroxidase staining was positive. Immunophenotyping was also ordered.
-What is the most likely diagnosis?
(Multiple Choice)
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What is the definition of acute leukemia, according to the World Health Organization?
(Essay)
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Predict the typical platelet concentration of a patient with AML.
(Multiple Choice)
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(82)
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.
-Which of the following laboratory findings would be most consistent with this clinical picture?
(Multiple Choice)
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Traditional therapy in APL includes pharmacological concentration of RA (ATRA) and chemotherapy.What is the function of the chemotherapy component in this treatment protocol?
(Multiple Choice)
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The patient presents with acute leukemia.The blast morphology is of neutrophil lineage with Auer rods and pseudo-Pelger-Huët nuclei; the immunophenotype is positive for CD33, CD13, CD34, and CD56 with a positive TdT, 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 cytotechemistry?
(Multiple Choice)
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A bone marrow sample is sent to the lab for cytochemical staining.MPO, SBB, and 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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The M:E ratio of a patient with AML typically displays which of the following?
(Multiple Choice)
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The WHO classification system of AML incorporates which of the following?
(Multiple Choice)
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All of the following AML subtypes have positive reactivity with myeloperoxidase stain except:
(Multiple Choice)
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A patient presents with bleeding, and is found to be in DIC.The peripheral smear contains hypergranular promyelocytes.The white count is slightly elevated.The bone marrow contains cells with multiple Auer rods with a clear blue cytoplasm.What is the probable type of AML?
(Multiple Choice)
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Which acute leukemia is characterized by a blast population with both myeloid and lymphoid markers on the same cell?
(Multiple Choice)
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