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. Thrombocytopenia is absent in: A. Disseminated intravascular coagulation B. Myelosclerosis C. Henoch-Schonlein purpura D. Wiskott-Aldrich syndrome 2 / 50 2. Which of the following is not a myelodysplastic syndrome (MDS)? A. Refractory anemia with ring sideroblasts B. Acute myelomonocytic leukemia C. Refractory anemia with excess blasts D. Refractory anemia 3 / 50 3. Packed red cells are constructed by: A. Precipitation B. Filtration C. Sedimentation D. Centrifugation 4 / 50 4. In chronic granulomatous disease, which is false? A. Diagnosed by amount of nitroblue tetrazolium reduction B. Prone to infection by staphylococci C. Difficulty in phagocytosis D. Neutrophil count is normal 5 / 50 5. Which of the following is not associated with hypersplenism? A. Pancytopenia B. Splenomegaly C. Hypocellular bone marrow D. Reversibility by splenectomy 6 / 50 6. In polycythaemia vera, which is not true? A. Increased LAP score B. Low level of erythropoietin C. High ESR D. High serum vitamin B12 level 7 / 50 7. Which of the following is false about methaemoglobinaemia? A. If exceeds >0.5 g/ dl, produces cyanotic hue B. Normal red cells contain <1 % methemoglobin C. Hereditary variety is due to deficiency of methemoglobin reductase D. Oral or I.V. methylene blue is treatment of choice 8 / 50 8. Warm-antibody mediated haemolysis is not found in: A. Non-Hodgkin's lymphoma B. Infectious mononucleosis C. Chronic lymphatic leukaemia D. SLE 9 / 50 9. Which is a bad prognostic sign of Hodgkin’s disease? A. Lymphocytopenia B. Thrombocytopenia C. Eosinophilia D. Reed-Sternberg cells in marrow 10 / 50 10. Sickle cell anaemia is associated with: A. Cerebral embolism B. Diastolic murmur over precordium C. Fish-mouth vertebrae D. High ESR 11 / 50 11. Features of sickle cell anaemia do not include: A. Nocturia B. Hypersplenism C. Leg ulcers D. Priapism 12 / 50 12. Which of the following is false in haemophilia? A. Normal prothrombin time B. Increased partial thromboplastin time C. von Willebrand antigens level is grossly diminished D. Absent factor VIII coagulant activity 13 / 50 13. Which of the following is false regarding Philadelphia chromosome? A. Diagnostic of CML B. Shortening of the long arm of chromosome G22 C. Found in lymphocytes D. Philadelphia -ve cases have a bad prognosis 14 / 50 14. vW antigen level is increased in: A. Multiple myeloma B. Pregnancy C. von Willebrand disease D. Lymphoma 15 / 50 15. Pseudolymphoma may be produced by all except: A. Lithium B. Primidone C. Cyclosporine D. Phenytoin 16 / 50 16. Which of the following anaemias is associated with splenomegaly? A. Sickle cell anemia B. Hereditary spherocytosis C. Aplastic anemia D. Chronic renal failure 17 / 50 17. Henoch-Schonlein purpura is not associated with: A. Intussusception B. Palpable purpura C. Thrombocytopenia D. Acute diffuse glomerulonephritis 18 / 50 18. Which of the following factors is unstable in stored blood? A. VII B. V C. II D. X 19 / 50 19. Sezary syndrome is: A. A variety of alopecia mucinosa B. B-cell lymphoma C. T-cell lymphoma D. Arsenical hyperkeratosis 20 / 50 20. G6PD may reflect a ‘false normal’ report in: A. Hairy cell leukemia B. Shortly after haemolysis C. Iron deficiency anemia D. Hypoplastic anemia 21 / 50 21. Circulating anticoagulants are found in: A. SLE B. Dermatomyositis C. Hairy cell leukemia D. Multiple myeloma 22 / 50 22. The prominent feature of idiopathic thrombocytopenic purpura (ITP) is: A. Presence of sternal tenderness B. Gum bleeding C. Moderate splenomegaly D. Fever 23 / 50 23. The half-life of a platelet is: A. 10-12 days B. 5-6 days C. 1-2 days D. 3-4 days 24 / 50 24. Which of the following may develop in sites other than bone marrow? A. Neutrophil B. Monocyte C. Lymphocyte D. Megakaryocyte 25 / 50 25. Schumm test is done to detect? A. Citrulline B. Methaemalbumin C. Haptoglobin D. Haemopexin 26 / 50 26. Which of the following is false in hereditary haemorrhagic telangiectasis? A. Telangiectasia does not blanch on pressure B. May have hematemesis C. Positive familial pattern D. Telangiectasia in skin and mucous membrane 27 / 50 27. Haemolytic anaemia is not produced by: A. Lithium B. Penicillin C. Quinidine D. Methyldopa 28 / 50 28. Pancytopenia may develop from all except: A. Acute myeloid leukemia (AML) B. Systemic lupus erythematosus C. Hemosiderosis D. Paroxysmal nocturnal hemoglobinuria (PNH) 29 / 50 29. Leucocyte alkaline phosphatase (LAP) score is high in all except: A. Polycythaemia vera B. Chronic myeloid leukaemia C. After steroid administration D. Myelosclerosis 30 / 50 30. Which of the following is not true in paroxysmal cold hemoglobinuria? A. IgG antibody-mediated B. Precipitated by exposure to cold C. Associated with mycoplasma infection D. Not a cold agglutinin disease 31 / 50 31. Which of the following is not true in thrombasthenia? A. Normal platelet count B. Prolonged clotting time C. Platelet aggregation defect D. Prolonged bleeding time 32 / 50 32. All are true regarding midline granuloma except: A. Produces perforation of nasal septum B. Pathological hallmark is non-caseating granuloma C. The treatment of choice is radiotherapy D. More common in men 33 / 50 33. Leucoerythroblastic blood picture may be seen in all except: A. Sickle cell anemia B. Myelophthisic anemia C. Gaucher's disease D. Myelofibrosis 34 / 50 34. Eosinophilia is caused by all except: A. Oxyphenbutazone B. Sulphonamides C. Iodides D. Nitrofurantoin 35 / 50 35. Conditions resistant to malaria are all except: A. Thalassemia major B. Sickle cell disease C. Duffy -ve blood group D. Hb C disease 36 / 50 36. Macrocytic-hypochromic anemia is found in: A. Pernicious anemia B. Iron deficiency anemia C. Pregnancy D. Thalassemia 37 / 50 37. Virchow’s node receives lymphatics from all except: A. Breast (left) B. Testes C. Prostate D. Stomach 38 / 50 38. Hepatosplenomegaly with lymphadenopathy is found in all except: A. Chronic myeloid leukemia B. Disseminated tuberculosis C. Lymphoma D. Acute lymphatic leukemia 39 / 50 39. The largest organ system’ in the human body is: A. Blood B. GI tract C. Endothelium D. Skin 40 / 50 40. Commonest pathogen involved in sickle cell anemia-induced osteomyelitis is: A. Nocardia B. Staphylococcus C. Streptococcus D. Salmonella 41 / 50 41. Decreased iron and decreased iron-binding capacity are seen in: A. Chronic infections B. Menorrhagia C. Intestinal resection D. Recurrent GI tract hemorrhage 42 / 50 42. All of the following produce microcytic anaemia except: A. Thalassemia B. Pernicious anemia C. Lead poisoning D. Sideroblastic anemia 43 / 50 43. Bone marrow examination is essential in: A. Acute lymphoblastic leukemia B. Hairy cell leukaemia C. Thalassemia D. Megaloblastic anemia 44 / 50 44. Cooley’s anemia is: A. Thalassemia major B. Aplastic anemia C. Sickle cell anemia D. Megaloblastic anemia 45 / 50 45. Non-Hodgkin’s lymphoma is classified under the name: A. Dorothy Reed B. Ann Arbor C. Rye D. Rappaport 46 / 50 46. Malignancy of which lineage is associated with autoimmune haemolytic anemia? A. T cell B. Pre-B cell C. B cell D. Pre-T cell 47 / 50 47. Waldeyer’s ring does not include: A. Submandibular glands B. Lingual tonsils C. Faucal tonsils D. Adenoids 48 / 50 48. Transient myeloproliferative disorder of the newborn is commonly seen in association with: A. Froehlich's syndrome B. Hurler syndrome C. Down's syndrome D. Ataxia telangiectasia 49 / 50 49. Which is not a vitamin K-dependent factor: A. Factor VII B. Factor VIII C. Factor II D. Factor X 50 / 50 50. Low-dose arsenic trioxide has recently been used in relapsed patients of: A. Acute lymphoblastic leukemia B. Hairy cell leukemia C. Acute promyelocytic leukemia D. Aplastic anemia LinkedIn Facebook Twitter VKontakte Visit our FB page Restart Quiz Send Feedback Previous Post Pulmonology Next Post Neurology
