Hematology Mcqs

Hematology MCQs 2003 MEDKAAU 20 MCQs 3 short Assays ---choice 2 ……………………………………… 1. Major hematopeotic embryo: A. Yolk sac B. Bone marrow C. liver D. spleen E. lymph nodes 2. All can cause Iron deficiency anemia EXCEPT: A. Menorrhagia B. bleeding from GIT C. Pregnancy. D. Transcoblamin 1 deficiency 3. 1ry site of folate absorption is: A. Proximal jejunum. B. Duodenum C. both D. neither 4. Which of the following test is most helpful in diagnosis of thalassemia : A. serum iron and iron binding capacity B. bone marrow iron stain C. hemoglobin electrophoresis 5. all can be associated with Sickle Cell Anemia EXCEPT: A. vasoocclusive cresis B. infection C. bleeding disease D. organ damage E. chest Syndrome F. Aplastic cresis 6. Anemia characterized by increase RBCs production is: A. chronic renal failure B. Hereditary Spherocytosis C. Fanconi's Anemia D. Anemia of chronic disease 7. All of the following common finding in Acute Lymphocytic leukemia EXCEPT:

A. epistaxis B. fever C. marked elevation in WBCs D. Gum hypertrophy 8. In Acute myelocytic leukemia all of the following correct EXCEPT : A. Bone marrow examination is essential diagnosis B. Philadelphia +ve chromosome C. more common in adult D. it is worse prognosis than chronic myeloid leukemia 9. the Philadelphia chromosome observed in which one of the following leukemia: A. chronic myeloid leukemia B. Acute Lymphocytic Leukemia C. Both D. Neither 10. Diagnostic criteria of 2ry polycythemia all of the following EXCEPT: A. smoking B. renal cyst C. a high altitude D. D.M 11. Haemophilia A ( factor IIIV deficiency) EXCEPT: A. All males with defective gene have hemophilia B. It is Autosomal dominant inheritance C. 50% of daughter's of hemophilic man are carrier D. 50% of daughter's of hemophilic man are diseased 12. Thrombocytopenia can be all of the following EXCEPT: A. ITP B. ALL C. AML D. Essential thrombocytopenia 13. R factor for venous thrombosis include all EXCEPT: A. immobilization B. Estrogen therapy C. Anti thrombin III deficiency D. Exercise 14. which can cause thrombosis: A. liver disease B. thrombocytopenia C. Anti phospholipid Syndrome

15. Blood Transfusion for all EXCEPT: A. Hepatitis B & C virus B. Hepatitis A virus C. Syphilis D. HIV 16.

The packed RBCs are stored at :

A. 4 degree Centigrade B. 30 degree Centigrade C. 37 degree Centigrade D. 20 degree Centigrade (note: platelets at room temperature=25)

17. Vitamin K dependent coagulation Factors may include all EXCEPT: A. Factor 2 B. Factor 7 C. Factor 9 D. Factor 11 18. All of the following features of Multiple Myeloma EXCEPT: A. Pathological fracture B. Increase plasma abnormal cells in bone marrow C. Increase peak serum of monoclonal protein in electrophoresis D. Increase Hemoglobin level 19. Hodgkin's Disease the most common histological subtype is: A. Lymphocytic predominant B. Mixed Cellularity C. Nodular sclerosing D. Lymphocyte depleted 20. In which of the following Hematological disorders the polymerase chain reaction is helpful: A. Megaloblastic anemia B. Hemolytic anemia C. Iron deficiency anemia D. Hemolytic malignancy

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Important Assays in the Revisions • One Assay about blood transfusion (complication immediate & delayed) • One Assay about Malignancy (Myeloma, lymphoma, Leukemia, major criteria of polycythemia) • One Assay about Benign (anemia, thrombocytopenia, acute blood loss)

• Approach a patient with

1.Thrombocytopenia *********** 2. Leukemia(Acute and chronic) *********** 3. Normocytic normochromic anemia 4. Acute Lymophocytic Anemia 5. Acute Lymphoblastic Anemia 6. Lymphoma *********** 7. Hemolytic Anemia 8. Myeloma

• Investigation of Iron deficiency anemia? • Risk factors of venous thrombosis? • What are the major criteria of polycythemia?( 1ry, 2ry ) *********** • What are the major criteria of MM? • What are the myeloproliferative disorders? (4) • M3 in AML (Associated with DIC, Gum hyperatrophy) • Benign WBCs ………..MCQs • Causes of (Leukocytosis, leukopenia, reticulocytosis……in tables) ………..MCQs • • • •

NOT

Treatment involved Common presentation of G6PD deficiency Common presentation of Sickle Cell Anemia Investigation P58…….Important.

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