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. Sideroblastic anemia may be treated by all except: A. Pyridoxine B. Desferrioxamine C. Androgens D. Hydroxyurea 2 / 50 2. All of the following may cause pain abdomen in thalassaemia major except: A. Splenic infarction B. Pigment stone-induced biliary colic C. Dragging pain due to huge splenomegaly D. Vasculitis 3 / 50 3. Bence-Jones proteins are derived from which type of globulin? A. Delta B. Alpha C. Gamma D. Beta 4 / 50 4. Cooley’s anemia is: A. Megaloblastic anemia B. Aplastic anemia C. Thalassemia major D. Sickle cell anemia 5 / 50 5. Hepatosplenomegaly with lymphadenopathy is found in all except: A. Chronic myeloid leukemia B. Lymphoma C. Disseminated tuberculosis D. Acute lymphatic leukemia 6 / 50 6. Spur cell anaemia is seen in: A. Myxoedema B. Lymphoma C. Cirrhosis of liver D. Uremia 7 / 50 7. All of the following produce microcytic anaemia except: A. Sideroblastic anemia B. Lead poisoning C. Thalassemia D. Pernicious anemia 8 / 50 8. Which of the following is false in haemophilia? A. von Willebrand antigens level is grossly diminished B. Increased partial thromboplastin time C. Normal prothrombin time D. Absent factor VIII coagulant activity 9 / 50 9. Myelophthisic anemia is characterised by all except: A. Caused by disseminated malignancy B. Neutropenia C. Basophilic stippling D. Leucoerythroblastic blood picture 10 / 50 10. Patients on aspirin will have: A. Prolonged clotting time B. Prolonged bleeding time C. Prolonged APTT D. Prolonged PT 11 / 50 11. Bone marrow examination is essential in: A. Acute lymphoblastic leukemia B. Thalassemia C. Hairy cell leukaemia D. Megaloblastic anemia 12 / 50 12. alpha-interferon is not beneficial in: A. Hairy cell leukemia B. Kaposi's sarcoma C. Chronic granulomatous disease D. Chronic myeloid leukaemia 13 / 50 13. Warm-antibody mediated haemolysis is not found in: A. SLE B. Chronic lymphatic leukaemia C. Infectious mononucleosis D. Non-Hodgkin's lymphoma 14 / 50 14. Burr cells in the blood are seen in: A. Myxoedema B. Uremia C. Hemolytic anemia D. Cirrhosis of liver 15 / 50 15. Epitrochlear adenopathy may be produced by all except: A. Tularemia B. Secondary syphilis C. Leprosy D. Sarcoidosis 16 / 50 16. Haemolytic anaemia is not produced by: A. Quinidine B. Penicillin C. Lithium D. Methyldopa 17 / 50 17. Which isolated coagulation factor deficiency causes thrombosis? A. Factor V B. Factor XII C. Factor VII D. Factor XI 18 / 50 18. Splenectomy is contraindicated in: A. Agnogenic myeloid metaplasia B. Marrow failure C. Pyruvate kinase deficiency D. Immune thrombocytopenic purpura 19 / 50 19. Malignancy of which lineage is associated with autoimmune haemolytic anemia? A. B cell B. Pre-T cell C. Pre-B cell D. T cell 20 / 50 20. Thrombasthenia may be seen in all of the following except: A. Paraproteinemia B. Diabetes mellitus C. Uremia D. Myeloproliferative disorders 21 / 50 21. Which of the following is associated with prolonged bleeding time? A. von Willebrand's disease B. Polycythaemia vera C. Antiphospholipid syndrome D. Hemophilia 22 / 50 22. Which is not true in relation to multiple myeloma? A. Response to Melphalan B. Moderate splenomegaly C. Renal failure D. Hyperviscosity syndrome 23 / 50 23. Carcinoembryonic antigen is the tumour marker of: A. Colorectal carcinoma B. Bronchogenic carcinoma C. Ovarian carcinoma D. Hepatocellular carcinoma 24 / 50 24. Which of the following is false regarding Philadelphia chromosome? A. Shortening of the long arm of chromosome G22 B. Diagnostic of CML C. Philadelphia -ve cases have a bad prognosis D. Found in lymphocytes 25 / 50 25. Which of the following is not found in eosinophilic granuloma? A. Affects young adults B. Osteolytic lesions in bone C. Eosinophilia D. Absence of systemic manifestations 26 / 50 26. Thrombocytopenia is absent in: A. Myelosclerosis B. Disseminated intravascular coagulation C. Wiskott-Aldrich syndrome D. Henoch-Schonlein purpura 27 / 50 27. Sickle cell anaemia is not complicated by: A. Osteomyelitis B. Congestive cardiac failure C. Pancreatitis D. Papillary necrosis 28 / 50 28. Transient myeloproliferative disorder of the newborn is commonly seen in association with: A. Ataxia telangiectasia B. Down's syndrome C. Hurler syndrome D. Froehlich's syndrome 29 / 50 29. Erythropoietin is secreted from all of the following tumours except: A. Oat cell carcinoma of lung B. Renal cell carcinoma C. Cerebellar hemangioblastoma D. Pheochromocytoma 30 / 50 30. Which of the following may develop in sites other than bone marrow? A. Lymphocyte B. Neutrophil C. Monocyte D. Megakaryocyte 31 / 50 31. Pancytopenia may develop from all except: A. Acute myeloid leukemia (AML) B. Systemic lupus erythematosus C. Paroxysmal nocturnal hemoglobinuria (PNH) D. Hemosiderosis 32 / 50 32. Raised Fe and normal TIBC are found in: A. Hemosiderosis B. Disseminated malignancy C. Thalassaemia major D. Rheumatoid arthritis 33 / 50 33. Which of the following is not true in thrombasthenia? A. Prolonged bleeding time B. Platelet aggregation defect C. Prolonged clotting time D. Normal platelet count 34 / 50 34. Acanthosis nigricans may be associated with all except: A. Diabetes mellitus B. Stein-Leventhal syndrome C. Ulcerative colitis D. Carcinoma of the stomach 35 / 50 35. Low-dose arsenic trioxide has recently been used in relapsed patients of: A. Hairy cell leukemia B. Aplastic anemia C. Acute lymphoblastic leukemia D. Acute promyelocytic leukemia 36 / 50 36. Which of the following is false about methaemoglobinaemia? A. Hereditary variety is due to deficiency of methemoglobin reductase B. If exceeds >0.5 g/ dl, produces cyanotic hue C. Oral or I.V. methylene blue is treatment of choice D. Normal red cells contain <1 % methemoglobin 37 / 50 37. Auer rods are found in: A. Blast crisis of CML B. Acute lymphatic leukemia (ALL) C. Blast crisis of CLL D. Acute myeloid leukaemia (AML) 38 / 50 38. Among the following, the treatment of choice in hairy cell leukaemia is: A. Corticosteroid B. Splenectomy C. Deoxycoformycin D. Hydroxyurea 39 / 50 39. Agranulocytosis may be seen in treatment with: A. Chlorpromazine B. Clonidine C. Clozapine D. Risperidone 40 / 50 40. Which of the following anaemias is associated with splenomegaly? A. Chronic renal failure B. Hereditary spherocytosis C. Aplastic anemia D. Sickle cell anemia 41 / 50 41. Coagulation factor deficient in stored blood is: A. IX B. II C. VII D. V 42 / 50 42. Total serum LDH is not raised in: A. Hemolysis B. Stroke C. AMI D. Crush injury 43 / 50 43. Macrocytic-hypochromic anemia is found in: A. Iron deficiency anemia B. Pregnancy C. Thalassemia D. Pernicious anemia 44 / 50 44. All of the following may complicate bone marrow transplantation except: A. Cataract formation B. Cardiomyopathy C. Leukoencephalopathy D. Emphysema 45 / 50 45. Which of the following is not true in paroxysmal cold hemoglobinuria? A. Associated with mycoplasma infection B. IgG antibody-mediated C. Not a cold agglutinin disease D. Precipitated by exposure to cold 46 / 50 46. HAM test (acid serum test), now an obsolete test, was used to diagnose: A. Myelodysplastic syndrome B. Paroxysmal nocturnal haemoglobinuria C. Hemolytic-uremic syndrome D. G6PD deficiency 47 / 50 47. The largest organ system’ in the human body is: A. Skin B. GI tract C. Blood D. Endothelium 48 / 50 48. Circulating anticoagulants are found in: A. Hairy cell leukemia B. Multiple myeloma C. Dermatomyositis D. SLE 49 / 50 49. 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 50 / 50 50. ‘Cast iron spleen’ is classically found in: A. Chronic myeloid leukemia (CML) B. Myelofibrosis C. Thalassemia major D. Tropical splenomegaly syndrome LinkedIn Facebook Twitter VKontakte Visit our FB page Restart Quiz Send Feedback Previous Post Pulmonology Next Post Neurology