Exam 16: Hemolytic Anemia: Immune Anemias
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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A patient is admitted with chest pain and extreme shortness of breath.Patient history is unremarkable except for ingestion of oral cefoxitin for the past 4 days.A DAT profile is positive with polyspecific AHG, negative with anti-IgG, and positive with anti-C3.The hemoglobin is 8.0 gm/dl.Based on these results, what mechanism of drug-induced hemolysis is present?
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(Multiple Choice)
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Correct Answer:
A
A patient with SLE shows evidence of decreased hemoglobin and ongoing hemolysis.The DAT is negative.Which of the following is the most likely explanation for these results?
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(Multiple Choice)
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Correct Answer:
D
2-14 days after a transfusion, a patient is cross-matched for another transfusion.Slight hemolysis and a positive DAT are found.What testing should follow?
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(Multiple Choice)
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Correct Answer:
B
The most likely cause of immediate hemolytic transfusion reaction is due to antibodies of which system?
(Multiple Choice)
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Paroxysmal cold hemoglobinuria is associated with viral and bacterial infections in children.With what other disease(s) is it associated?
(Multiple Choice)
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Which of the following set of results is consistent with a diagnosis of WAIHA?
Polyspecific AHG anti-IgG anti-C3 a. Positive positive negative b. Positive negative negative c. Negative positive positive d. Positive negative positive
(Essay)
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A Group O, Rh negative woman with no evidence of antibodies delivers her first child who shows a slightly decreased hemoglobin and the presence of spherocytes on the peripheral blood film.The DAT is positive with polyspecific AHG and anti-IgG.The baby is Group A, Rh negative and is slightly jaundiced with a bilirubin of 2.1 mg/dl.What is the most likely cause of the baby's jaundice?
(Multiple Choice)
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A patient on α-methyldopa may develop a type of drug-induced immune hemolysis that mimics what condition?
(Multiple Choice)
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A 44 year old female presents for her routine examination.She complains of tiredness and difficulty in breathing when she exerts herself.Her DAT is positive with polyspecific AHG and anti-IgG.Her hemoglobin is 7.5 gm/dl and her indices suggest a normocytic, normochromic anemia.Her peripheral blood smear shows the presence of spherocytes.What is the most likely diagnosis?
(Multiple Choice)
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Compare the differences in the activation of complement that lead to intravascular hemolysis or extravascular hemolysis.
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A patient's hemoglobin went from a value of 13.0 gm/dl after transfusion to 10.6 gm/dl 3 days after transfusion.What is the most likely type of transfusion reaction?
(Multiple Choice)
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Which of the following is an example of an anemia that occurs as a result of antibody development to an antigen that the individual lacks?
(Multiple Choice)
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ABO incompatibility is associated with which type of transfusion reaction?
(Multiple Choice)
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Acute hemolytic transfusion reaction is characterized by which of the following?
(Multiple Choice)
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A sample demonstrates a DAT profile that is positive with polyspecific AHG, negative with anti-IgG, and positive with anti-C3.If the Donath-Landsteiner test was also positive, what should the CLS do?
(Multiple Choice)
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Explain why the DAT profile in CAD is reactive only with polyspecific AHG and anti-C3 but not with anti-IgG.
(Essay)
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Autoantibodies associated with CAD are directed against what antigen system?
(Multiple Choice)
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