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Hematology MCQs for Medical Students

This document contains a series of 37 multiple choice questions related to hematology. The questions cover topics such as causes of anemia, characteristics of various blood disorders, signs and symptoms, diagnostic features, treatment options and more. Philadelphia chromosome is incorrectly found in lymphocytes. Hereditary spherocytosis is associated with splenomegaly. Vasculitis does not typically cause abdominal pain in thalassemia major.

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Aydaross Kamal
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0% found this document useful (1 vote)
1K views5 pages

Hematology MCQs for Medical Students

This document contains a series of 37 multiple choice questions related to hematology. The questions cover topics such as causes of anemia, characteristics of various blood disorders, signs and symptoms, diagnostic features, treatment options and more. Philadelphia chromosome is incorrectly found in lymphocytes. Hereditary spherocytosis is associated with splenomegaly. Vasculitis does not typically cause abdominal pain in thalassemia major.

Uploaded by

Aydaross Kamal
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Hematology MCQ H.Y.

1-Which of the following is wrong concerning Philadelphia chromosome:


a -shortening of long arm of chromosome 22
b -Philadelphia –ve cases have bad prognosis
c -diagnostic of CML
d -found in lymphocytes(√)
2 -the commonest cause of jaundice in thalassemia is:
a -viral hepatitis c
b -iron deposition in liver
c -viral hepatitis B
d -haemolysis (√)
3-Waldeyer' ring does not include:
a -faucal tonsils
b -submandibular glands(√)
c -adenoids
d-lingual tonsils
4-whitch of the following anemias is associated with splenomegaly:
a -chronic renal failure
b -aplastic anemia
c -hereditary spherocytosis(√)
d -sickle cell anaemia
5 -all may cause abdominal pain in thalassemia major except:
a -vasculitis(√)
b -splenic infarction
c -dragging pain dt huge splenomegaly
d -pigment stones in gall bladder
6 -Virchow's node receives lymphatics from all except:
a -testes
b -stomach
c-prostate(√)
d -breast
7 -all produce microcytic anemia except:
a -sideroblastic an.
b -thalassemia
c-pernicious anemia(√)
d-lead poisoning
8 -Basophilic stippling is classically seen in:
1
Hematology MCQ H.Y.M

a -CML
b -myelosclerosis
c -chronic lead poisoning(√)
d -iron def anemia
9-Increase Fe & normal TIBC are found in:
a -thalassemia major
b -haemosidrosis
c-rheumatoid arthritis(√)
d-dissiminated malignancy
10 -Non thrombocytopenic purpurais seen in all except:
a-vasculitis
b-uraemia
c-hereditary haemorrhagic telangectasia
d-SLE(√)
11 -Gum bleeding is characteristic of all except:
a-chronic phenytoin therapy(√)
b-aplastic an.
c-scurvy
d-haemophilia
12-Which of the following is not true in thrombathenia:
a-prolonged bleeding time
b-normal plat .Count
c-plat .Aggregation defect
d-prolonged clotting time(√)
13 -Which is not associated with hypersplenism:
a-splenomegaly
b-pancytopenia
c-hyper cellular bone marrow(√)
d-reversibility by splenectomy
14-splenectomy is curative in:
a-G6PD def.
b-ITP
c-thalassemia
d-hereditary sphrocytosis(√)
15-Plummer Vinson syndrome is not associated with:
a-angular stomatitis
b-splenomegaly
c -clubbing(√)
2
Hematology MCQ H.Y.M

d -post cricoid web


16 haemolytic anemia is not produced by:
a-penicillin
b-lithium(√)
c -Quinidine
d -methyldopa
17-sideroblastic anemia may be treated by all except:
a-pyridoxine
b-hydroxy urea(√)
c -desferroxamine
d-androgens
18-Henoch schonlien purpura is not associated with:
a-thrombocytopenia(√)
b -palpable purpura
c-intussusception
d-acute diffuse glomerulonephritis
19 -Outstanding feature of ITP:
a-fever
b -gum bleeding(√)
c -moderate splenomegaly
d -sterna tenderness
20 -Thrombocytopenia is absent in:
a-DIC
b-Wiskottt Aldrich syndrome
c -Henoch schonlien purpura (√)
d -myelosclerosis
21 -Cooley's anemia is:
a-Sickle cell an.
b-thalassemia major(√)
c -high ESR
d-aplastic an.
22 -presence of an .–jaundice –splenomegaly with increase MCH is
seen in:
a-liver cirrhosis
b-th.major
c-PNH
d-herditary spherocytosis(√)
23-all may complicate BM transplantation except:
3
Hematology MCQ H.Y.M

a-cataract formation
b-leucoencephalopathy
c -cardiomyopathy
d -emphysema(√)
24-incorrect about pernicious an:.
a-hyperchlorhydria(√)
b-premature graying of hair
c -anti intrinsic factor antibody in 60℅ of pts.
d -gastric polyp may occur
25-Busulfan therapy lead to all except:
a-hyperpigmentation
b-pulm .Fibrosis
c-optic neuritis(√)
d -BM suppression
26-increase serum iron –decrease IBC a feature of:
a-Hookworm infestation
b-sideroblastic an(.√)
c-alcoholic liver dis.
d-th.major
27 -hepato-splenomegaly with lymphadenopathy occur in all
except:
a-ALL
b-lymphoma
c-CML(√)
d-dissiminated TB
28 – sickle cell an .Is not complicated by:
A -papillary necrosis
b-pancreatitis(√)
c -osteomyelitis
d -CHF
29 -decrease iron &decrease iron binding capacity are seen in:
a-recurrent GIT bleeding
b -intestinal resection
c -chronic infection(√)
d-menorrhagia
30-Plat .Transfusion is not indicated in:
a-aplastic an.
b-uraemia with bleeding
4
Hematology MCQ H.Y.M

c-DIC
d-immunogenic thrombocytopenia(√)
31-best ttt modality in CML is:
a-hydroxyurea
b-allogenic BMT(√)
c-interferon alpha
d-radiotherapy
32-G6PD reflect false normal report in:
a-iron def .an.
b -hypoplastic an.
c-hairy cell leuk.
d-shortly after haemolysis(√)
33-half life of plat .Is:
a-1-2days
b-3-4days(√)
c-5-6days
d-7-8days
34-Macrocytosis is a characteristic of all except:
a-an .Of myxedema
b -methotrexate induced
c -chronic alcoholism induced liver dis.
d -SLE(√)
35-which is associated with prolonged bleeding time:
a-polythycemia vera
b-Von Willebrand dis(.√)
c -antiphospholipid syndrome
d -haemophilia
36-peripheral bl .Picture is most useful in:
a-NHL
b-multiple myeloma
c-myelodysplastic syndrome
d -CML(√)
37 -splenectomy is contraindicated in:
a-pyruvate kinase def.
b-ITP
c-BM failure(√)
d-angiogenic myeloid metaplasia( myeloproliferative.

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