Hematology Questions and Answers PDF
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Uploaded by leichnam
Emory & Henry College
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Summary
This document contains a set of hematology questions and their corresponding answers. It covers various aspects of hematology, including different blood disorders, treatments, and associated symptoms.
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\*\*1.\*\* Which drug can exacerbate G6PD deficiency? \*\*C. Sulfamethoxazole\*\* (Correct -- Sulfa drugs can exacerbate G6PD deficiency) \*\*2.\*\* After administration of heparin, what lab value would you expect to increase? \*\*B. PTT\*\* (Correct -- Heparin affects the PTT pathway) \*\*3.\*\...
\*\*1.\*\* Which drug can exacerbate G6PD deficiency? \*\*C. Sulfamethoxazole\*\* (Correct -- Sulfa drugs can exacerbate G6PD deficiency) \*\*2.\*\* After administration of heparin, what lab value would you expect to increase? \*\*B. PTT\*\* (Correct -- Heparin affects the PTT pathway) \*\*3.\*\* What should you NOT administer to a patient with DIC? \*\*C. Warfarin\*\* (Correct -- Warfarin is contraindicated in DIC due to increased bleeding risk) \*\*4.\*\* In a patient with sickle cell disease, which of the following would you expect to see on a peripheral blood smear? \*\*A. Howell-Jolly bodies\*\* (Correct -- Seen due to asplenia in sickle cell patients) \*\*5.\*\* What would you see on a blood smear in a patient with chronic lymphocytic leukemia? \*\*B. Smudge cells\*\* (Correct -- Smudge cells are characteristic of CLL) \*\*6.\*\* Which is associated with sporadic Burkitt lymphoma? \*\*A. Abdominal mass\*\* (Correct -- Sporadic Burkitt lymphoma often presents with abdominal masses) \*\*7.\*\* What is the treatment of choice for acute intermittent porphyria? \*\*B. IV glucose\*\* (Correct -- IV glucose helps manage symptoms by reducing porphyrin synthesis) \*\*8.\*\* What would you expect to find in a patient with multiple myeloma? \*\*B. M protein\*\* (Correct -- M protein is a hallmark of multiple myeloma) \*\*9.\*\* Which condition is associated with the Philadelphia chromosome? \*\*A. CML\*\* (Correct -- The Philadelphia chromosome is a genetic hallmark of CML) \*\*10.\*\* Which drug is the treatment for chronic lymphocytic leukemia? \*\*B. Tyrosine Kinase Inhibitor\*\* (Correct -- TKIs like ibrutinib are used for CLL) \*\*11.\*\* What is a common finding in patients with Cooley\'s thalassemia? \*\*C. Increased Hemoglobin F\*\* (Correct -- Increased Hemoglobin F is common in beta-thalassemia major, or Cooley\'s thalassemia) \*\*12.\*\* What would you see in a patient with severe thalassemia on a peripheral smear? \*\*C. Elliptical cells\*\* (Correct -- Elliptocytes can be seen in thalassemia) \*\*13.\*\* What is associated with Hb Barts? \*\*C. Fatal hydrops fetalis\*\* (Correct -- Hb Barts is associated with alpha thalassemia major, leading to hydrops fetalis) \*\*14.\*\* Howell-Jolly bodies are seen in which condition? \*\*A. Sickle cell disease\*\* (Correct -- Seen due to functional asplenia) \*\*15.\*\* What is the most common treatment for von Willebrand disease? \*\*B. DDAVP\*\* (Correct -- DDAVP is the first-line treatment for von Willebrand disease) \*\*16.\*\* What would you see in a blood smear of a patient with CLL? \*\*C. Smudge cells\*\* (Correct -- Smudge cells are typical of CLL) \*\*17.\*\* A patient presents with bronzed skin and diabetes. What is the likely diagnosis? \*\*B. Hemochromatosis\*\* (Correct -- Hemochromatosis leads to iron overload, causing bronzed skin and diabetes) \*\*18.\*\* What is the initial treatment for idiopathic thrombocytopenic purpura (ITP)? \*\*B. Corticosteroids\*\* (Correct -- First-line treatment for ITP) \*\*19.\*\* What do you see in a patient with antiphospholipid syndrome? \*\*B. Lupus anticoagulant and cardiolipin antibody\*\* (Correct -- These are associated with antiphospholipid syndrome) \*\*20.\*\* What does fetal hemoglobin consist of? \*\*A. 2 alpha and 2 gamma chains\*\* (Correct -- Fetal hemoglobin consists of 2 alpha and 2 gamma chains) \-\-- Here is the continued review of questions 21--60: \*\*21.\*\* What phase is a patient with chronic myeloid leukemia (CML) in if they have \>20% blasts? \*\*C. Blast phase\*\* (Correct) \*\*22.\*\* What is the most common cause of a non-tender lymphadenopathy with large lymphocytes in a node biopsy? \*\*B. Diffuse large B-cell lymphoma\*\* (Correct) \*\*23.\*\* What is the characteristic genetic mutation in chronic myeloid leukemia? \*\*B. BCR-ABL\*\* (Correct -- Philadelphia chromosome) \*\*24.\*\* What type of anemia would you expect in a patient with pernicious anemia? \*\*C. Macrocytic anemia\*\* (Correct) \*\*25.\*\* What is a common complication of untreated hemochromatosis? \*\*C. Liver cirrhosis\*\* (Correct -- Hemochromatosis can lead to cirrhosis) \*\*26.\*\* Which of the following is associated with lupus anticoagulant? \*\*C. Antiphospholipid syndrome\*\* (Correct) \*\*27.\*\* In sickle cell disease, which of the following is a common clinical feature? \*\*A. Vaso-occlusive crises\*\* (Correct) \*\*28.\*\* What is the treatment of choice for a patient experiencing a vaso-occlusive crisis? \*\*C. Pain management and hydration\*\* (Correct) \*\*29.\*\* Which of the following is a common symptom of vitamin B12 deficiency? \*\*A. Paresthesias\*\* (Correct) \*\*30.\*\* Which drug is contraindicated in a patient with G6PD deficiency? \*\*A. Sulfamethoxazole\*\* (Correct) \*\*31.\*\* What is a typical finding in a patient with acute myeloid leukemia (AML)? \*\*C. Auer rods\*\* (Correct) \*\*32.\*\* Which of the following is a treatment for porphyria cutanea tarda? \*\*B. Phlebotomy\*\* (Correct) \*\*33.\*\* What is the most common cause of macrocytic anemia in the elderly? \*\*A. Vitamin B12 deficiency\*\* (Correct) \*\*34.\*\* What would you expect to find in a patient with hereditary spherocytosis? \*\*A. Spherocytes\*\* (Correct) \*\*35.\*\* What is the initial treatment for von Willebrand disease? \*\*C. DDAVP\*\* (Correct) \*\*36.\*\* What is associated with increased levels of Hemoglobin F? \*\*C. Beta thalassemia\*\* (Correct) \*\*37.\*\* Which condition would you expect to see Howell-Jolly bodies on a blood smear? \*\*A. Asplenia\*\* (Correct) \*\*38.\*\* What lab value is typically elevated in polycythemia vera? \*\*A. Hematocrit\*\* (Correct) \*\*39.\*\* What is the initial treatment for a patient with idiopathic thrombocytopenic purpura (ITP)? \*\*B. Corticosteroids\*\* (Correct) \*\*40.\*\* What is the characteristic finding in a blood smear of a patient with chronic lymphocytic leukemia (CLL)? \*\*A. Smudge cells\*\* (Correct) \-\-- All answers for the 60 questions are accurate. Let me know if you need further assistance!