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. Which of the following anaemias is associated with splenomegaly? A. Hereditary spherocytosis B. Sickle cell anemia C. Chronic renal failure D. Aplastic anemia 2 / 50 2. Decreased iron and decreased iron-binding capacity are seen in: A. Menorrhagia B. Chronic infections C. Recurrent GI tract hemorrhage D. Intestinal resection 3 / 50 3. Circulating anticoagulants are found in: A. SLE B. Multiple myeloma C. Hairy cell leukemia D. Dermatomyositis 4 / 50 4. Eosinophilia is caused by all except: A. Nitrofurantoin B. Sulphonamides C. Oxyphenbutazone D. Iodides 5 / 50 5. Which of the following is not true regarding features of hyperviscosity syndrome? A. Fluctuating consciousness B. Raynaud's phenomenon C. Thrombotic episodes D. Central cyanosis 6 / 50 6. Intravascular half-life of factor-VIII is: A. 4-5 days B. 5 hours C. 1-3 days D. 12 hours 7 / 50 7. Low-dose arsenic trioxide has recently been used in relapsed patients of: A. Aplastic anemia B. Acute lymphoblastic leukemia C. Hairy cell leukemia D. Acute promyelocytic leukemia 8 / 50 8. Haemolytic anaemia is not produced by: A. Quinidine B. Lithium C. Penicillin D. Methyldopa 9 / 50 9. Sickle cell anaemia is not complicated by: A. Osteomyelitis B. Papillary necrosis C. Pancreatitis D. Congestive cardiac failure 10 / 50 10. Erythropoietin is increased in all except: A. Hepatocellular carcinoma B. Pancreatic carcinoma C. Cerebellar haemangioblastoma D. Renal cell carcinoma 11 / 50 11. Which is not a vitamin K-dependent factor: A. Factor X B. Factor II C. Factor VIII D. Factor VII 12 / 50 12. Coombs positive haemolytic anaemia is a feature of: A. Systemic lupus erythematosus (SLE) B. Polyarteritis nodosa (PAN) C. Thrombotic thrombocytopenic purpura (TTP) D. Hemolytic-uremic syndrome (HUS) 13 / 50 13. Bence-Jones proteins are derived from which type of globulin? A. Alpha B. Gamma C. Delta D. Beta 14 / 50 14. Waldenstrom’s macroglobulinaemia commonly has all the features except: A. Anemia B. Hyper viscosity syndrome C. Lymphadenopathy D. Renal failure 15 / 50 15. In polycythaemia vera, which is not true? A. Increased LAP score B. High serum vitamin B12 level C. Low level of erythropoietin D. High ESR 16 / 50 16. All are features of tropical pulmonary eosinophilia except: A. Eosinophilia >3000/mm^3 B. Miliary mottling in chest X-ray C. High IgE level D. Response to albendazole therapy 17 / 50 17. Para-hemophilia is a deficiency of factor: A. V B. IX C. von Willebrand's D. XI 18 / 50 18. Increased serum iron and reduced iron-binding capacity are features of: A. Thalassemia major B. Hookworm infestation C. Alcoholic liver disease D. Sideroblastic anemia 19 / 50 19. Bone marrow examination is essential in: A. Thalassemia B. Acute lymphoblastic leukemia C. Hairy cell leukaemia D. Megaloblastic anemia 20 / 50 20. Thrombasthenia may be seen in all of the following except: A. Uremia B. Diabetes mellitus C. Myeloproliferative disorders D. Paraproteinemia 21 / 50 21. Macrocytosis of RBC is characteristic of all except: A. Chronic alcoholism-induced liver disease B. Methotrexate-induced C. Systemic lupus erythematosus D. Anemia of myxoedema 22 / 50 22. Which of the following is false in hereditary haemorrhagic telangiectasis? A. Telangiectasia in skin and mucous membrane B. Positive familial pattern C. May have hematemesis D. Telangiectasia does not blanch on pressure 23 / 50 23. Hand-Schwier-Christian disease does not have: A. Diabetes mellitus B. Hepatosplenomegaly C. Hypercholesterolemia D. Exophthalmos 24 / 50 24. All of the following may complicate bone marrow transplantation except: A. Leukoencephalopathy B. Cataract formation C. Cardiomyopathy D. Emphysema 25 / 50 25. Which isolated coagulation factor deficiency causes thrombosis? A. Factor XII B. Factor XI C. Factor V D. Factor VII 26 / 50 26. Which of the following is not associated with hypersplenism? A. Pancytopenia B. Reversibility by splenectomy C. Hypocellular bone marrow D. Splenomegaly 27 / 50 27. The best treatment modality in chronic myeloid leukaemia is: A. Allogenic bone marrow transplantation B. Radiotherapy C. Interferon-alpha D. Hydroxyurea 28 / 50 28. Malignancy of which lineage is associated with autoimmune haemolytic anemia? A. Pre-B cell B. T cell C. Pre-T cell D. B cell 29 / 50 29. Busulfan therapy may lead to all except: A. Optic neuritis B. Bone marrow suppression C. Hyperpigmentation D. Pulmonary fibrosis 30 / 50 30. In chronic granulomatous disease, which is false? A. Difficulty in phagocytosis B. Neutrophil count is normal C. Prone to infection by staphylococci D. Diagnosed by amount of nitroblue tetrazolium reduction 31 / 50 31. Histiocytosis-X disease does not include: A. Hand-Schuller-Christian disease B. Letterer-Siwe disease C. Unifocal eosinophilic granuloma D. Niemann-Pick disease 32 / 50 32. Leucoerythroblastic blood picture may be seen in all except: A. Gaucher's disease B. Sickle cell anemia C. Myelofibrosis D. Myelophthisic anemia 33 / 50 33. Which of the following is not associated with a microangiopathic blood picture? A. Thrombotic thrombocytopenic purpura B. Infectious mononucleosis (glandular fever) C. Meningococcal septicaemia D. Severe burns 34 / 50 34. HAM test (acid serum test), now an obsolete test, was used to diagnose: A. Hemolytic-uremic syndrome B. G6PD deficiency C. Paroxysmal nocturnal haemoglobinuria D. Myelodysplastic syndrome 35 / 50 35. ‘Suggilations’ are haemorrhagic spots in the size of: A. > 10 mm in diameter B. 2-5 mm in diameter C. 1-2 mm in diameter D. > 20 mm in diameter 36 / 50 36. Commonest pathogen involved in sickle cell anemia-induced osteomyelitis is: A. Nocardia B. Streptococcus C. Salmonella D. Staphylococcus 37 / 50 37. The commonest cause of jaundice in thalassaemia is: A. Iron deposition in liver B. Viral hepatitis B C. Viral hepatitis C D. Hemolysis 38 / 50 38. Disseminated intravascular coagulation (DIC) may be seen in all except: A. Rocky Mountain spotted fever B. Giant hemangioma C. Amniotic fluid embolism D. Diabetes mellitus 39 / 50 39. Leucocyte alkaline phosphatase (LAP) score is diminished in: A. Thalassemia major B. Sickle cell anemia C. Lymphoma D. Paroxysmal nocturnal hemoglobinuria (PNH) 40 / 50 40. Spur cell anaemia is seen in: A. Uremia B. Cirrhosis of liver C. Myxoedema D. Lymphoma 41 / 50 41. The presence of anemia, jaundice and splenomegaly with increased mean corpuscular haemoglobin concentration (MCHC) is seen in: A. Hereditary spherocytosis B. Paroxysmal nocturnal hemoglobinuria (PNH) C. Cirrhosis of liver D. Thalassemia major 42 / 50 42. Henoch-Schonlein purpura is not associated with: A. Palpable purpura B. Intussusception C. Acute diffuse glomerulonephritis D. Thrombocytopenia 43 / 50 43. Acanthosis nigricans may be associated with all except: A. Ulcerative colitis B. Stein-Leventhal syndrome C. Carcinoma of the stomach D. Diabetes mellitus 44 / 50 44. Alopecia mucinosa may be seen in: A. Amyloidosis B. Pancreatic carcinoma C. Mycosis fungoides D. Carcinoid syndrome 45 / 50 45. Punctate basophilia is seen in all except: A. Megaloblastic anemia B. Iron deficiency anemia C. Thalassemia D. Lead poisoning 46 / 50 46. ‘Cast iron spleen’ is classically found in: A. Thalassemia major B. Chronic myeloid leukemia (CML) C. Myelofibrosis D. Tropical splenomegaly syndrome 47 / 50 47. Giant lysosomal granules in granulocytes associated with albinism is known as: A. May-Hegglin anomaly B. Schultz syndrome C. Niemann-Pick disease D. Chediak-Higashi syndrome 48 / 50 48. Hemolytic-uraemic syndrome (HUS) is not characterised by: A. Hematuria B. Thrombocytosis C. Uremia D. Segmented RBCs in peripheral smear 49 / 50 49. Pelger-Huet anomaly is: A. Hereditary hypersegmentation of neutrophils B. Faulty maturation of platelets C. Presence of Dohle bodies in neutrophils D. Hereditary hyposegmentation of neutrophils 50 / 50 50. Among the following, the treatment of choice in hairy cell leukaemia is: A. Hydroxyurea B. Corticosteroid C. Deoxycoformycin D. Splenectomy LinkedIn Facebook Twitter VKontakte Visit our FB page Restart Quiz Send Feedback Previous Post Pulmonology Next Post Neurology