Explore topic-wise MCQs in Medical Subjects .

This section includes 313 Mcqs, each offering curated multiple-choice questions to sharpen your Medical Subjects knowledge and support exam preparation. Choose a topic below to get started.

151.

Lepra cells seen in leprosy are_____________?

A. Lymphocytes
B. Plasma cells
C. Vacuolated Histocytes
D. Neutrophils
Answer» D. Neutrophils
152.

Lepra cells are seen in abundance in_______________?

A. Tuberculoid leprosy
B. Lepromatous leprosy
C. Histoid leprosy
D. Intermediate leprosy
Answer» C. Histoid leprosy
153.

Left side heart failure results in______________?

A. Oedema of lungs
B. Oedema of spleen
C. Oedema of legs
D. Oedema of liver
Answer» B. Oedema of spleen
154.

Large open wounds that are characterized by tissue loss and repaired by formation of granulation tissue in the floor of the wound is characteristic of______________?

A. Secondary healing
B. Primary healing
C. Cicatrisation
D. Regeneration
Answer» B. Primary healing
155.

Kviem’s test is diagnostic test for_________________?

A. Actinomycosis
B. Diphtheria
C. Tuberculosis
D. Sarcoidosis
Answer» E.
156.

Keratin pearls with downward proliferation of epithelial masses is characteristic of_______________?

A. Squamous cell carcinoma
B. Basal cell carcinoma
C. Epidermoid carcinoma
D. Melanoma
Answer» B. Basal cell carcinoma
157.

Intrinsic factor for absorption of Vit B12 secreted in ______________?

A. Duodenum
B. Stomach
C. Intestine
D. Ileum
Answer» C. Intestine
158.

Inflammation is characterized by________________?

A. Transudation -> exudation -> oedena
B. Oedema -> exudation
C. Exudation -> transudation -> oedema
D. Only by exudation -> oedema
Answer» B. Oedema -> exudation
159.

Infarcts are not common in______________?

A. Liver
B. Lung
C. Kidney
D. Both A and B
Answer» E.
160.

Increased proliferation of cells is called_______________?

A. Hypertrophy
B. Atrophy
C. Hyperplasia
D. Metaplasia
Answer» D. Metaplasia
161.

Increased levels of haemoglobin A2 is characteristic of________________?

A. Sickle cell trait
B. b-thalassaemia crait
C. Glucose-6 phosphate dehydrogenase deficiency
D. a-Thalassamia
Answer» C. Glucose-6 phosphate dehydrogenase deficiency
162.

Increased iron binding capacity and decreased serum iron is seen in which anemia________________?

A. Iron deficiency
B. Aplastic
C. Sickle cell
D. Chronic infections
Answer» B. Aplastic
163.

Increased bleeding time is seen in all except______________?

A. Thrombocytopenia
B. Von Willebrand disease
C. Hemophilia
D. Ehlers danlos syndrome
Answer» D. Ehlers danlos syndrome
164.

Increase in number of RBC is seen in ____________?

A. Neutropenia
B. Leukemia
C. Polycythemia
D. Anaemia
Answer» D. Anaemia
165.

Incomplete fractures of the bone are called___________?

A. Comminuted fracture
B. Compound fracture
C. Simple fracture
D. Green stick fracture
Answer» E.
166.

Incidence of most common malignant tumours in women is_____________?

A. Breast
B. Lung
C. Cervix
D. Ovary
Answer» B. Lung
167.

In which one of the following organs the venous emboli are most often iodged ?

A. Lungs
B. Kidneys
C. Intestines
D. Heart
Answer» B. Kidneys
168.

In Troisiers sign the lymph nodes involved are_________________?

A. Right axillary nodes
B. Left axillary nodes
C. Right supraclavicular nodes
D. Left supraclavicular nodes
Answer» E.
169.

In sickle cell anaemia there is_____________?

A. 75 to 100% haemoglobins
B. 10 to 20% haemoglobins
C. 20 to 30% haemoglobins
D. 50 to 60% haemoglobins
Answer» B. 10 to 20% haemoglobins
170.

In sickle cell anemia there is substitution of_________________?

A. Valine for glutamic acid at the sixth position of beta chain
B. Phenylalanine for glutamic acid
C. Tyrosine for valine at the 6th position at beta chain
D. All of the above
Answer» B. Phenylalanine for glutamic acid
171.

In megaloblastic anaemia the cells are___________________?

A. Macrocytic hyperchromic
B. Macrocytic hypochromic
C. Macrocytic normochromic
D. None of the above
Answer» D. None of the above
172.

In left ventricular cardiac failure there is_____________?

A. Passive Congestion in lungs
B. Passive congestion in liver
C. Active hyperemia in lungs
D. None of the above
Answer» B. Passive congestion in liver
173.

In leucopenia, which cell type is predominantly involved ?

A. Erythrocytes
B. Granulocytes
C. Eosinophils
D. Monocytes
Answer» C. Eosinophils
174.

In iron deficiency anemia there is_________________?

A. Decrease in hemoglobin
B. Increase in hemoglobin
C. Increase in palatelets
D. Decrease in platelets
Answer» B. Increase in hemoglobin
175.

In hypovolemic shock_____________?

A. The central venous pressure ins high
B. The extremities are pale, cold and sweating
C. There is always s site of bleeding
D. Urine output is unaffected
Answer» C. There is always s site of bleeding
176.

In Hodgkin’s disease the lymphoa cells seen are__________________?

A. Eosinophilis
B. Plasma cells
C. Reed-sternberg cells
D. Giant cells
Answer» D. Giant cells
177.

In hemephilic patient which of the following should not be given_______________?

A. Factor VIII concentrate
B. Cryoprecipitate
C. EACA
D. Platelet factor
Answer» E.
178.

In hemorrhager lost plasma is replaced by______________?

A. Bone marrow
B. Kidney
C. Spleen
D. Muscle
Answer» C. Spleen
179.

In granuloma, epithelial and giant cells are derived from_____________?

A. T cells
B. B cells
C. Plasma cells
D. Monocyte
Answer» E.
180.

IN fanconi anemia there is a_______________?

A. Deficiency of copper
B. Mutation of DNA repair gene
C. No increased risk of Sq. cell carcinoma
D. Purely nutritional disorder etiology
Answer» C. No increased risk of Sq. cell carcinoma
181.

In dysplasia mitotic figures are seen in_________________?

A. In basal layers of epithelium
B. In surface layers only
C. From basal layer to surface
D. None of the above
Answer» D. None of the above
182.

In chronic, granulomatous inflammation, which of the following processes is most likely to predominate ?

A. Exudation
B. Congestion
C. Transudation
D. Proliferation
Answer» E.
183.

In acute inflammation, immediate transient permeability in cells is increased by__________?

A. Direct injury & necrosis
B. Endothelial Gaps by histamine
C. Leucocyte mediated endothelial injury
D. Increased tissue oncotic pressure
Answer» C. Leucocyte mediated endothelial injury
184.

In a thrombus, the dark lines of zahn are due to_______________?

A. Coagulated fibrin
B. Aggregated proteins
C. Aggregated platelets
D. Aggregated R.B.C
Answer» E.
185.

Important components of collagen synthesis, wound strength and contraction include all of the following EXCEPT ?

A. Fibroblasts
B. Myofibroblasts
C. Vitamin C
D. Vitamin D
Answer» E.
186.

Immune response to tumour is mediated by_______________?

A. Cytotoxic T – lymphocytes
B. Natural killer cells
C. Humoral mechanism
D. All of the above
Answer» E.
187.

IL-1 helps in_____________?

A. Stimulation of T-lymphocytes
B. Inhibits of B-lymphocytes
C. Inhibits the chemotaxis of neutrophils and macrophages
D. Decreases firbroblast and bone resorption activity
Answer» B. Inhibits of B-lymphocytes
188.

Hypoxic death leads to__________________?

A. Liquefactive necrosis
B. Coagulative nacrosis
C. Caseous necrosis
D. Fat necrosis
Answer» C. Caseous necrosis
189.

Hypovolemic shock develops after loss of______________?

A. 10% blood
B. 20% blood
C. 30% blood
D. 40% blood
Answer» E.
190.

Hyper segmented neutrophils are seen in_________________?

A. Megaloblastic anemia
B. Iron deficiency anemia
C. Thalassemia
D. Idiopathic thrombocytopenic purpura
Answer» B. Iron deficiency anemia
191.

Hydrolytic degeneration is characterised by__________________?

A. Caseation
B. Coagulation
C. Liquefaction
D. Fibrinoid
Answer» D. Fibrinoid
192.

HOX gene is responsible for which malformation_____________?

A. Polysyndactyly
B. Holoprosencephaly
C. Mayer Rokitansky syndrome
D. Gorlin syndrome
Answer» B. Holoprosencephaly
193.

Hodgkin’s lymphoma can be distinguished from non – Hodgkin’s lymphomas by_________________?

A. Reed – Sternberg cells
B. Systemic manifestations
C. Occurence in young adults
D. All of the above
Answer» E.
194.

Highly infection stage of syphilis______________?

A. Primary
B. Secondary
C. Tetriary
D. Congenital
Answer» C. Tetriary
195.

Heterozygous sickle cell anaemia gives protection against______________?

A. G6PD
B. Malaria
C. Thalassemia
D. Dengue fever
Answer» C. Thalassemia
196.

Hemophilics show_________________?

A. Increased bleeding time and clotting time
B. Decreased bleeding time and clotting time
C. Decreased bleeding time and increased clotting time
D. Normal bleeding time and increased clotting time
Answer» E.
197.

Hemophilia_______________?

A. Affects males and females equally
B. Increased clotting time in all patients
C. Nerve blocks can be given safely
D. Is a congenital disorder
Answer» C. Nerve blocks can be given safely
198.

Hemophilia is best treated by _____________?

A. dried freeze plasma
B. factor VIII concentrate
C. Whole blood
D. cryoprecipitate
Answer» C. Whole blood
199.

Hemophilia A is caused due to deficiency of___________________?

A. Factor X
B. Factor XI
C. Factor IX
D. Factor VIII
Answer» E.
200.

Heart failure cells are____________?

A. Fibrocytes in myocardium
B. Aschoji’s giant cells
C. Heamosiderin laden macrophages in alveoli
D. Hypertrophic myocardial fibres
Answer» D. Hypertrophic myocardial fibres