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 contraindicated in: A. Agnogenic myeloid metaplasia B. Marrow failure C. Immune thrombocytopenic purpura D. Pyruvate kinase deficiency 2 / 50 2. Commonest pathogen involved in sickle cell anemia-induced osteomyelitis is: A. Nocardia B. Salmonella C. Staphylococcus D. Streptococcus 3 / 50 3. Red cell osmotic fragility is increased in: A. Hereditary spherocytosis B. Thalassemia major C. Iron deficiency anemia D. Hb C disease 4 / 50 4. The half-life of albumin is: A. 10-14 days B. 1-2 days C. 20-22 days D. 16-20 days 5 / 50 5. Megakaryocytosis in bone marrow is seen in all except: A. Chronic myeloid leukemia B. Myeloid metaplasia C. Idiopathic thrombocytopenic purpura D. Polycythemia vera 6 / 50 6. Sickle cell anaemia is associated with: A. Diastolic murmur over precordium B. High ESR C. Cerebral embolism D. Fish-mouth vertebrae 7 / 50 7. The best treatment modality in chronic myeloid leukaemia is: A. Hydroxyurea B. Radiotherapy C. Allogenic bone marrow transplantation D. Interferon-alpha 8 / 50 8. Auer rods are found in: A. Acute myeloid leukaemia (AML) B. Acute lymphatic leukemia (ALL) C. Blast crisis of CML D. Blast crisis of CLL 9 / 50 9. Histiocytosis-X disease does not include: A. Unifocal eosinophilic granuloma B. Hand-Schuller-Christian disease C. Letterer-Siwe disease D. Niemann-Pick disease 10 / 50 10. The half-life of a platelet is: A. 3-4 days B. 5-6 days C. 10-12 days D. 1-2 days 11 / 50 11. All of the following may complicate bone marrow transplantation except: A. Cataract formation B. Cardiomyopathy C. Leukoencephalopathy D. Emphysema 12 / 50 12. Serum alkaline phosphatase level in multiple myeloma is usually? A. Normal B. High C. Fluctuates D. Low 13 / 50 13. Leucocyte alkaline phosphatase (LAP) score is high in all except: A. Chronic myeloid leukaemia B. Polycythaemia vera C. Myelosclerosis D. After steroid administration 14 / 50 14. Peripheral blood picture is the most useful diagnostic aid in: A. Chronic myeloid leukemia B. Myelodysplastic syndrome C. Non-Hodgkin's lymphoma D. Multiple myeloma 15 / 50 15. Punctate basophilia is seen in all except: A. Megaloblastic anemia B. Iron deficiency anemia C. Lead poisoning D. Thalassemia 16 / 50 16. Which of the following is false regarding Philadelphia chromosome? A. Philadelphia -ve cases have a bad prognosis B. Found in lymphocytes C. Diagnostic of CML D. Shortening of the long arm of chromosome G22 17 / 50 17. All of the following may produce agranulocytosis except: A. Methimazole B. Gold salts C. Methyldopa D. Chloramphenicol 18 / 50 18. vW antigen level is increased in: A. Lymphoma B. von Willebrand disease C. Pregnancy D. Multiple myeloma 19 / 50 19. Which is a bad prognostic sign of Hodgkin’s disease? A. Lymphocytopenia B. Eosinophilia C. Reed-Sternberg cells in marrow D. Thrombocytopenia 20 / 50 20. Wiskott-Aldrich syndrome does not feature: A. Eczema B. Thrombocytopenia C. Repeated infections D. Hemolytic anemia 21 / 50 21. Tumour lysis syndrome produces all except: A. Hypercalcemia B. Hyperphosphatemia C. Hyperkalemia D. Hyperuricemia 22 / 50 22. Spur cell anaemia is seen in: A. Cirrhosis of liver B. Lymphoma C. Uremia D. Myxoedema 23 / 50 23. Non-thrombocytopenic purpura is seen in all except: A. Uremia B. Vasculitis C. Hereditary hemorrhagic telangiectasis D. SLE 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. Iron transport protein is: A. Ferritin B. Transferrin C. Transcobalamin II D. Haptoglobin 26 / 50 26. Which of the following is not seen in sickle cell anaemia? A. Isosthenuria B. Leucopenia C. Leg ulcers D. Corkscrew vessel in bulbar conjunctiva 27 / 50 27. Schumm test is done to detect? A. Methaemalbumin B. Haemopexin C. Haptoglobin D. Citrulline 28 / 50 28. Vitamin C is used in low dose (3 mg/kg) in thalassaemia major as in high dose, it produces: A. Cardiotoxicity B. Nephrotoxicity C. Neurotoxicity D. Hepatotoxicity 29 / 50 29. Features of sickle cell anaemia do not include: A. Leg ulcers B. Hypersplenism C. Nocturia D. Priapism 30 / 50 30. Coagulation factor deficient in stored blood is: A. VII B. V C. II D. IX 31 / 50 31. Which of the following is false about methaemoglobinaemia? A. Oral or I.V. methylene blue is treatment of choice B. Hereditary variety is due to deficiency of methemoglobin reductase C. If exceeds >0.5 g/ dl, produces cyanotic hue D. Normal red cells contain <1 % methemoglobin 32 / 50 32. The commonest cause of jaundice in thalassaemia is: A. Iron deposition in liver B. Hemolysis C. Viral hepatitis C D. Viral hepatitis B 33 / 50 33. G6PD may reflect a ‘false normal’ report in: A. Hypoplastic anemia B. Hairy cell leukemia C. Shortly after haemolysis D. Iron deficiency anemia 34 / 50 34. Which of the following is not associated with hypersplenism? A. Reversibility by splenectomy B. Hypocellular bone marrow C. Splenomegaly D. Pancytopenia 35 / 50 35. Transient myeloproliferative disorder of the newborn is commonly seen in association with: A. Ataxia telangiectasia B. Froehlich's syndrome C. Hurler syndrome D. Down's syndrome 36 / 50 36. Warm-antibody mediated haemolysis is not found in: A. Non-Hodgkin's lymphoma B. Chronic lymphatic leukaemia C. Infectious mononucleosis D. SLE 37 / 50 37. All of the following produce microcytic anaemia except: A. Sideroblastic anemia B. Lead poisoning C. Thalassemia D. Pernicious anemia 38 / 50 38. Which of the following factors is unstable in stored blood? A. VII B. X C. V D. II 39 / 50 39. Pelger-Huet anomaly is: A. Hereditary hyposegmentation of neutrophils B. Faulty maturation of platelets C. Presence of Dohle bodies in neutrophils D. Hereditary hypersegmentation of neutrophils 40 / 50 40. Plasmapheresis may be done in all except: A. Myasthenia gravis B. Cryoglobulinemia C. Hypoplastic anemia D. Goodpasture's disease 41 / 50 41. Sezary syndrome is: A. A variety of alopecia mucinosa B. T-cell lymphoma C. B-cell lymphoma D. Arsenical hyperkeratosis 42 / 50 42. Total serum LDH is not raised in: A. Stroke B. AMI C. Crush injury D. Hemolysis 43 / 50 43. Circulating anticoagulants are found in: A. Multiple myeloma B. Dermatomyositis C. SLE D. Hairy cell leukemia 44 / 50 44. Agranulocytosis may be seen in treatment with: A. Risperidone B. Chlorpromazine C. Clonidine D. Clozapine 45 / 50 45. Which of the following is not a myeloproliferative disorder? A. Chronic myeloid leukemia B. Essential thrombocytopenia C. Polycythemia vera D. Myeloid metaplasia 46 / 50 46. The most effective treatment of polycythaemia vera is: A. Exchange transfusion B. Fresh frozen plasma C. Phlebotomy D. Splenectomy 47 / 50 47. Leucoerythroblastic blood picture may be seen in all except: A. Sickle cell anemia B. Myelofibrosis C. Gaucher's disease D. Myelophthisic anemia 48 / 50 48. Basophilic stippling is classically seen in: A. Chronic lead poisoning B. Iron deficiency anemia C. Myelosclerosis D. Chronic myeloid leukemia 49 / 50 49. Which of the following is not a myelodysplastic syndrome (MDS)? A. Refractory anemia B. Refractory anemia with excess blasts C. Refractory anemia with ring sideroblasts D. Acute myelomonocytic leukemia 50 / 50 50. In polycythaemia vera, which is not true? A. Low level of erythropoietin B. High serum vitamin B12 level C. High ESR D. Increased LAP score LinkedIn Facebook Twitter VKontakte Visit our FB page Restart Quiz Send Feedback Previous Post Pulmonology Next Post Neurology