Exam 15: Megaloblastic and Nonmegaloblastic Macrocytic Anemias
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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All of the following disorders can lead to macrocytic anemia except:
(Multiple Choice)
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Megaloblastic anemia is most often caused by deficiencies of what two components?
(Multiple Choice)
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An analyzed blood specimen reveals the following: the MCV is increased,the hemoglobin level is decreased,and the reticulocyte count is normal or low.What test could give more information on the cause of the anemia without drawing another blood specimen?
(Multiple Choice)
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The nuclear cytoplasmic asynchronous morphology in megaloblastosis is best characterized by:
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It is much easier to become folate-deficient than B₁₂ -deficient because:
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The defect in DNA synthesis associated with megaloblastic anemia affects which cells?
(Multiple Choice)
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Which of the following is found in megaloblastic anemia but not in nonmegaloblastic macrocytic anemia?
(Multiple Choice)
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The majority of PA patients have antibodies against what component necessary for vitamin B₁₂ absorption?
(Multiple Choice)
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Patients with blind loop syndrome can have vitamin B₁₂ deficiency complications resulting from:
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5-7.Use this case to answer the following questions.A 55-year-old male consulted his physician because of weakness,lightheadedness,vertigo,and angina.The patient also complained of sores on his tongue.The physical examination revealed jaundice.The pulse rate was increased,and the spleen and liver were slightly enlarged.The tongue appeared smooth and bright red in color.Family history revealed no clues.Neurological exam revealed quickening of reflex responses.Patient history indicated a total gastrectomy five years earlier for stomach cancer and intermittent heart problems that had not required surgery.The physician ordered the following tests:
-All of the following are expected laboratory findings of PA except:

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