Exam 27: Precursor Lymphoid Neoplasms
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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A phenotype workup is performed on a patient suspected to have ALL. The results indicate that some of the leukemic cells express myeloid markers, whereas others express T-cell markers. What is the most likely reason for this occurrence?
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Correct Answer:
B
Define acute undifferentiated leukemia and explain why it is difficult to identify.
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Acute undifferentiated leukemias is an acute leukemia in which the morphology, cytochemistry, and immunophenotype of the proliferating blasts lack sufficient information to classify them as myeloid or lymphoid origin. They are difficult to identify by conventional methods because they share common detectable markers of multiple lineages.
A 5-year-old patient has been diagnosed with Pre-B-cell ALL. Routine cytogenetic analysis confirms the presence of the Philadelphia chromosome. What does this mean for the patient?
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(Multiple Choice)
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Correct Answer:
C
As part of their disease progression, ALL patients are at risk for developing which of the following?
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Which of the following is a classic morphologic finding in the peripheral blood in ALL?
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Which of the following cytochemical stains would be most helpful in differentiating AML from ALL?
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A patient with ALL underwent chemotherapy. Results from hematologic, cytogenetic, and molecular analyses indicated that the patient entered complete remission. Four years later, on routine follow-up, the peripheral blood results for the patient were in the normal range, and cytogenetic analysis revealed no abnormalities, but molecular analysis showed BCR/ABL1 transcripts that were found in the blasts at diagnosis 4 years ago. This patient can be said to:
(Multiple Choice)
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A peripheral blood smear from a patient with acute leukemia displayed a homogeneous population of small blasts with scanty cytoplasm. Based on this information, which WHO classification is described?
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Which of the following markers would be helpful in differentiating cortical T-cell ALL from medullary T-cell ALL?
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What cytochemical stains are negative in ALL but positive in AML?
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ALL most often arises from a defect in which of the following?
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Which of the following cytochemical stains would be positive in this case?
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Which phase of leukemia treatment is considered to induce complete remission of the disease, eradicating the leukemic blast population?
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A patient, 2 years of age, presents with general fatigue, pallor, fever, and weight loss. The morphological exam reveals a normal leukocyte count, marked neutropenia, and thrombocytopenia with 35% blasts. A bone marrow smear reveals hypercellularity with neoplastic lymphoid cells. What immunophenotypic testing would be indicated for this patient?
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Which leukemia reveals the laboratory findings of TdT+, CD7+, and CD3+?
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The WHO defines acute lymphoblastic leukemia as having a blast count that is which of the following?
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The WHO classification of subgroups of ALL uses which of these criteria to help define the categories?
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Which of the following is a positive predictive factor in children with precursor B-ALL?
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