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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, reticulocytosisin tables)


..MCQs

NOT

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

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