Exam 27: Precursor Lymphoid 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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A technologist is reviewing a patient's blood smear.She notices that 85% blasts are present but is having a difficult time identifying the lineage.Cytochemical staining is subsequently performed,and the results for MPO,SBB,NSE,and PAS are negative.Based on this information,what is the most likely lineage of the unknown blasts?
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(Multiple Choice)
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Correct Answer:
B
Which markers are found on lymphoblasts?
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(Multiple Choice)
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Correct Answer:
D
Questions 8-10: Use this case to answer the following questions:
A 6-year-old boy was taken to see his pediatrician because of tiny pinpoint spots that had appeared on his upper torso 3 days earlier.A CBC revealed 70% blasts,and a platelet count of 18 × 10⁹/L.A bone marrow aspirate and biopsy indicate a diagnosis of ALL.
-Which of the following cytochemical stains would be positive in this case?
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(Multiple Choice)
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Correct Answer:
D
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?
(Multiple Choice)
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Questions 8-10: Use this case to answer the following questions:
A 6-year-old boy was taken to see his pediatrician because of tiny pinpoint spots that had appeared on his upper torso 3 days earlier.A CBC revealed 70% blasts,and a platelet count of 18 × 10⁹/L.A bone marrow aspirate and biopsy indicate a diagnosis of ALL.
-Cytogenetic analysis confirms the presence of t(1;14).This verifies which of the following types of ALL?
(Multiple Choice)
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Define acute undifferentiated leukemia and explain why it is difficult to identify.
(Essay)
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ALL most often arises from a defect in which of the following?
(Multiple Choice)
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Which of the following patient populations is most commonly afflicted with ALL?
(Multiple Choice)
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Which of the following is a positive predictive factor in children with precursor B-ALL?
(Multiple Choice)
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An immunoglobulin (Ig)gene rearrangement can be identified in all of the following acute lymphoblastic leukemias except:
(Multiple Choice)
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Summarize and explain why patients develop the clinical signs and symptoms oberserved in patients with ALL.
(Essay)
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Which of the following markers would be helpful in differentiating cortical T-cell ALL from medullary T-cell ALL?
(Multiple Choice)
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Which of the following is a classic morphologic finding in the peripheral blood in ALL?
(Multiple Choice)
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Which of the following cytochemical stains would be most helpful in differentiating AML from ALL?
(Multiple Choice)
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A patient has been diagnosed with B-cell ALL.Immunophenotyping has been ordered to confirm the subtype.Which markers would be ideal to help differentiate Pre-B-cell ALL from Pro-B-cell ALL?
(Multiple Choice)
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The WHO defines acute lymphoblastic leukemia as having a blast count that is which of the following?
(Multiple Choice)
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B-lymphoblasts in ALL exhibit which one of the following markers that is helpful in their identification?
(Multiple Choice)
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As part of their disease progression,ALL patients are at risk for developing which of the following?
(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?
(Multiple Choice)
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