Hematology Home Hematology 0% 13 votes, 0 avg 40 Hematology Welcome to Hematology Quiz. There are 50 shot-stemmed, single-best type Hematology questions. We have a collection of over 100 questions. Contact us and get a free link in case you are interested. 1 / 50 1. Splenectomy is virtually curative in: A. Hereditary spherocytosis B. G6PD deficiency C. Idiopathic thrombocytopenic purpura (ITP) D. Thalassemia 2 / 50 2. Peripheral blood picture is the most useful diagnostic aid in: A. Multiple myeloma B. Non-Hodgkin's lymphoma C. Chronic myeloid leukemia D. Myelodysplastic syndrome 3 / 50 3. Histiocytosis-X disease does not include: A. Niemann-Pick disease B. Letterer-Siwe disease C. Unifocal eosinophilic granuloma D. Hand-Schuller-Christian disease 4 / 50 4. Leucocyte alkaline phosphatase (LAP) score is diminished in: A. Thalassemia major B. Sickle cell anemia C. Paroxysmal nocturnal hemoglobinuria (PNH) D. Lymphoma 5 / 50 5. Which test detects haemolytic anemia? A. Occult blood test in stool B. Coombs' test C. Benedict's test D. Schilling test 6 / 50 6. Which of the following is not true in thrombotic thrombocytopenic purpura? A. Early development of acute renal failure B. Fluctuating consciousness C. Fragmented platelets D. Coombs -ve hemolysis 7 / 50 7. alpha-interferon is not beneficial in: A. Chronic granulomatous disease B. Chronic myeloid leukaemia C. Hairy cell leukemia D. Kaposi's sarcoma 8 / 50 8. The presence of anemia, jaundice and splenomegaly with increased mean corpuscular haemoglobin concentration (MCHC) is seen in: A. Cirrhosis of liver B. Hereditary spherocytosis C. Paroxysmal nocturnal hemoglobinuria (PNH) D. Thalassemia major 9 / 50 9. Busulfan therapy may lead to all except: A. Hyperpigmentation B. Pulmonary fibrosis C. Bone marrow suppression D. Optic neuritis 10 / 50 10. Which of the following is not associated with hypersplenism? A. Reversibility by splenectomy B. Hypocellular bone marrow C. Pancytopenia D. Splenomegaly 11 / 50 11. Which of the following is not seen in hemolytic-uraemic syndrome? A. Positive Coombs test B. Thrombocytopenia C. Hypofibrinogenaemia D. High creatinine level 12 / 50 12. Thrombasthenia may be seen in all of the following except: A. Uremia B. Myeloproliferative disorders C. Paraproteinemia D. Diabetes mellitus 13 / 50 13. All of the following may cause pain abdomen in thalassaemia major except: A. Splenic infarction B. Dragging pain due to huge splenomegaly C. Pigment stone-induced biliary colic D. Vasculitis 14 / 50 14. Lifespan of platelets is: A. 9-11 days B. 5-7 days C. 13-15 days D. 2-4 days 15 / 50 15. Auer rods are found in: A. Blast crisis of CLL B. Blast crisis of CML C. Acute lymphatic leukemia (ALL) D. Acute myeloid leukaemia (AML) 16 / 50 16. Which of the following is not found in eosinophilic granuloma? A. Osteolytic lesions in bone B. Affects young adults C. Eosinophilia D. Absence of systemic manifestations 17 / 50 17. All of the following are seen in intravascular haemolysis except: A. High plasma haemopexin B. High urinary urobilinogen C. High urinary haemosiderin D. Reticulocytosis 18 / 50 18. Malignancy of which lineage is associated with autoimmune haemolytic anemia? A. Pre-B cell B. B cell C. T cell D. Pre-T cell 19 / 50 19. Decreased iron and decreased iron-binding capacity are seen in: A. Intestinal resection B. Recurrent GI tract hemorrhage C. Menorrhagia D. Chronic infections 20 / 50 20. Bone marrow examination is essential in: A. Hairy cell leukaemia B. Thalassemia C. Acute lymphoblastic leukemia D. Megaloblastic anemia 21 / 50 21. Basophilia is classically found in: A. Melanoma B. Non-Hodgkin's lymphoma C. Hodgkin's disease C. D. Chronic myeloid leukaemia 22 / 50 22. Pelger-Huet anomaly is: A. Faulty maturation of platelets B. Presence of Dohle bodies in neutrophils C. Hereditary hyposegmentation of neutrophils D. Hereditary hypersegmentation of neutrophils 23 / 50 23. Microcytic hypochromic anaemia is characteristic of: A. Persons who are true vegetarians B. Munchausen's syndrome C. Pseudohypoparathyroidism D. Patterson-Kelly syndrome 24 / 50 24. Palpable purpura is seen in: A. Idiopathic thrombocytopenic purpura B. Quinine therapy C. Leucocytoclastic vasculitis D. Heparin-associated thrombocytopenia 25 / 50 25. Non-thrombocytopenic purpura is seen in all except: A. Vasculitis B. Hereditary hemorrhagic telangiectasis C. SLE D. Uremia 26 / 50 26. Carcinoembryonic antigen is the tumour marker of: A. Colorectal carcinoma B. Bronchogenic carcinoma C. Ovarian carcinoma D. Hepatocellular carcinoma 27 / 50 27. Macrocytosis of RBC is characteristic of all except: A. Systemic lupus erythematosus B. Methotrexate-induced C. Anemia of myxoedema D. Chronic alcoholism-induced liver disease 28 / 50 28. Which of the following is not a myeloproliferative disorder? A. Essential thrombocytopenia B. Myeloid metaplasia C. Polycythemia vera D. Chronic myeloid leukemia 29 / 50 29. Sideroblastic anemia may be treated by all except: A. Pyridoxine B. Androgens C. Hydroxyurea D. Desferrioxamine 30 / 50 30. The most sensitive and specific test for diagnosis of iron deficiency anaemia is: A. Serum iron level B. Serum ferritin level C. Serum transferrin receptor population D. Percentage of transferrin saturation 31 / 50 31. Which is a bad prognostic sign of Hodgkin’s disease? A. Eosinophilia B. Reed-Sternberg cells in marrow C. Lymphocytopenia D. Thrombocytopenia 32 / 50 32. Red cell osmotic fragility is increased in: A. Hereditary spherocytosis B. Hb C disease C. Thalassemia major D. Iron deficiency anemia 33 / 50 33. Features of sickle cell anaemia do not include: A. Leg ulcers B. Nocturia C. Hypersplenism D. Priapism 34 / 50 34. HAM test (acid serum test), now an obsolete test, was used to diagnose: A. Hemolytic-uremic syndrome B. Paroxysmal nocturnal haemoglobinuria C. Myelodysplastic syndrome D. G6PD deficiency 35 / 50 35. Serum alkaline phosphatase level in multiple myeloma is usually? A. Normal B. Fluctuates C. High D. Low 36 / 50 36. Cooley’s anemia is: A. Aplastic anemia B. Megaloblastic anemia C. Sickle cell anemia D. Thalassemia major 37 / 50 37. Which is not an example of microangiopathic haemolytic anemia? A. Paroxysmal cold hemoglobinuria B. Thrombotic thrombocytopenic purpura C. Hemolytic-uremic syndrome D. Disseminated intravascular coagulation 38 / 50 38. Giant lysosomal granules in granulocytes associated with albinism is known as: A. Schultz syndrome B. Chediak-Higashi syndrome C. May-Hegglin anomaly D. Niemann-Pick disease 39 / 50 39. Intravascular half-life of factor-VIII is: A. 1-3 days B. 5 hours C. 12 hours D. 4-5 days 40 / 50 40. Circulating anticoagulants are found in: A. Multiple myeloma B. Hairy cell leukemia C. Dermatomyositis D. SLE 41 / 50 41. Multiple myeloma does not feature: A. Hyperglobulinemia B. High Phosphate C. High Calcium D. High Uric acid 42 / 50 42. Sezary syndrome is: A. Arsenical hyperkeratosis B. B-cell lymphoma C. A variety of alopecia mucinosa D. T-cell lymphoma 43 / 50 43. Which of the following may develop in sites other than bone marrow? A. Megakaryocyte B. Lymphocyte C. Monocyte D. Neutrophil 44 / 50 44. In polycythaemia vera, which is not true? A. Low level of erythropoietin B. Increased LAP score C. High ESR D. High serum vitamin B12 level 45 / 50 45. Post-splenectomy peripheral blood picture does not contain: A. Howell-Jolly bodies B. Heinz bodies C. Dohle bodies D. Target cells 46 / 50 46. Chloroma is found in: A. Chronic myeloid leukemia (CML) B. Non-Hodgkin's lymphoma (NHL) C. Acute lymphatic leukemia (ALL) D. Acute myeloid leukemia (AML) 47 / 50 47. In chronic granulomatous disease, which is false? A. Prone to infection by staphylococci B. Neutrophil count is normal C. Difficulty in phagocytosis D. Diagnosed by amount of nitroblue tetrazolium reduction 48 / 50 48. Transient myeloproliferative disorder of the newborn is commonly seen in association with: A. Down's syndrome B. Froehlich's syndrome C. Ataxia telangiectasia D. Hurler syndrome 49 / 50 49. Henoch-Schonlein purpura is not associated with: A. Intussusception B. Acute diffuse glomerulonephritis C. Palpable purpura D. Thrombocytopenia 50 / 50 50. The most effective treatment of polycythaemia vera is: A. Splenectomy B. Fresh frozen plasma C. Exchange transfusion D. Phlebotomy LinkedIn Facebook Twitter VKontakte Visit our FB page Restart Quiz Send Feedback Previous Post Pulmonology Next Post Neurology