Exam 24: Acute Lymphoblastic 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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Which markers are found on lymphoblasts?
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(Multiple Choice)
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Correct Answer:
D
Explain the molecular and cytogenetic profile of a patient with Burkitt's ALL.
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(Essay)
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Correct Answer:
a.Translocation of the MYC gene 8q24) to the heavy chain region on chromosome 14 t8,14)) or to light chain loci on chromosome 2p12 t2,8))
b.Molecular assays: clonal rearrangement of immunoglobulin heavy and light chain genes
Which phase of leukemia treatment is considered to induce complete remission of the disease, eradicating the leukemic blast population?
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(Multiple Choice)
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Correct Answer:
A
What cytochemical stains are negative in ALL but positive in AML?
(Multiple Choice)
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Which of the following patient populations is most commonly afflicted with ALL?
(Multiple Choice)
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Use the case below to answer the following questions:
A mother takes her 6-year-old boy to see the pediatrician because of tiny pinpoint spots that appeared on his upper torso 3 days prior. The pediatrician orders a CBC, and it comes back abnormal. There are 70% blasts present, with a platelet count of 18 x 10⁹/L. A bone marrow aspirate and biopsy are performed, and confirm ALL. Cytogenetic and molecular testing was also ordered, but no results were present yet.
-Cytogenetic analysis confirms the presence of t (1, 14).This verifies which of the following types of ALL?
(Multiple Choice)
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Which leukemia reveals the laboratory findings of TdT+, CD7+, and CD3+?
(Multiple Choice)
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Patients with ALL are at risk for developing which types of symptoms? Explain your answer.
(Essay)
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Use the case below to answer the following questions:
A mother takes her 6-year-old boy to see the pediatrician because of tiny pinpoint spots that appeared on his upper torso 3 days prior. The pediatrician orders a CBC, and it comes back abnormal. There are 70% blasts present, with a platelet count of 18 x 10⁹/L. A bone marrow aspirate and biopsy are performed, and confirm ALL. Cytogenetic and molecular testing was also ordered, but no results were present yet.
-Which of the following cytochemical stains would be positive in this case?
(Multiple Choice)
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ALL most often arises from a defect in which of the following?
(Multiple Choice)
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Large cells with abundant, intensely basophilic cytoplasm with prominent cytoplasmic vacuolization are identified on a peripheral smear.Multiple basophilic nucleoli are present.A starry sky appearance is seen with fields of basophilic leukemic blasts with benign macrophages that have ingested tumor cells.What leukemia should be suspected with this morphology?
(Multiple Choice)
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Name at least five classifications of ALL, and explain how they are different.
(Essay)
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A peripheral blood smear of an ALL patient is displaying a homogeneous population of small blasts with scanty cytoplasm.Based on this information, what FAB classification of ALL is it?
(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 with ALL underwent chemotherapy.Results from hematologic, cytogenetic, and molecular analyses indicated that he entered complete remission.Four years later, on his routine follow-up, the peripheral blood results were in the normal range, and cytogenetic analysis revealed no abnormalities, but molecular analysis showed BCR/ABL 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 phenotype workup is performed on a suspected ALL patient.The results come back indeterminate based on evaluation of all common ALL antigens.What is the most likely reason for this occurrence?
(Multiple Choice)
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A technologist is reviewing a blood smear of a patient.She notices 85% blasts present, but is having a difficult time identifying the lineage.Cytochemical staining is subsequently performed, and the results for MPO, SBB, and NSE come back negative.Based on this information, what is the most likely lineage of the unknown blasts?
(Multiple Choice)
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Acute lymphoblastic leukemia is defined by the WHO as having a blast count that is which of the following?
(Multiple Choice)
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Morphological differences between ALL and Burkitt-type ALL include which of the following?
(Multiple Choice)
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A patient has been confirmed with B cell ALL.Confirmation of ALL subtype has been inconclusive based on the tests conducted.Immunophenotyping has been ordered as a last means of confirming 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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