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Latest Medical MCQs – Competitive Diseases of Blood And Lymphnodes ( Pathology ) MCQs

Latest Medical MCQs – Competitive Diseases of Blood And Lymphnodes ( Pathology ) MCQs

This post is comprising of latest ” ( Pathology ) MCQs – Latest Competitive Medical MCQs “. Here you’ll get latest Software engineering mcqs for written test, interview with answers. If you want to improve your knowledge regarding Software engineering then read these mcqs of Design of Steel Structures.

Latest Medical MCQs

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Latest Diseases of Blood And Lymphnodes ( Pathology ) Mcqs

The most occurred mcqs of Diseases of Blood And Lymphnodes ( Pathology ) in past papers. Past papers of Diseases of Blood And Lymphnodes ( Pathology ) Mcqs. Past papers of Diseases of Blood And Lymphnodes ( Pathology ) Mcqs . Mcqs are the necessary part of any competitive / job related exams. The Mcqs having specific numbers in any written test. It is therefore everyone have to learn / remember the related Diseases of Blood And Lymphnodes ( Pathology ) Mcqs. The Important series of Diseases of Blood And Lymphnodes ( Pathology ) Mcqs are given below:

A patient’s urine with a particular protein appears normal, but on standing it becomes dark. The dark colour disappears on heating. The patent is suffering from______________?

A. Infectious mononcleosis
B. Multiple myeloma
C. Osteoporosis
D. T – cell tumour

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

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

The characteristic finding in chronic myeloid leukemia is______________?

A. Reduced score of alkaline phosphatase in granulocytes
B. Total lack of platelets
C. Reduced score of acid phosphatase in granulocytes
D. Total lack of neutrophils

Sickle cell anemia precipitates when______________?

A. There is dehydration
B. Increased viscosity of blood
C. Oxygen tension goes down
D. All of the above

Neurologic abnormalities occur with_______________?

A. Foliate deficiency anemia
B. Vitamin B12 deficiency anemia
C. Pernicious anemia
D. Both B and C

Deposition of bile pigment in the basal ganglia is called________________?

A. Haemosiderosis
B. Kernicterus
C. jaundice
D. All of the above

A shift to left indicates an increase in number of______________?

A. immature neutrophils
B. matures neutrophils
C. erythrocytes
D. Platelets

Increased bleeding time is seen in all except______________?

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

The following are recognized causes of neutropenia Except_______________?

A. Corticosteroid therapy
B. Aplastic anemia
C. Typhoid fever
D. Viral infection

Prothrombin time indicates the integrity of ____________________?

A. Capillary function
B. Extrinsic pathway
C. Intrinsic pathway
D. All of the above

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

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

Which of the following is a nutritional deficiency anemia______________?

A. sickle cell anemia
B. aplastic anemia
C. megaloblastic anemia
D. hemolytic anemia

IN fanconi anemia there is a_______________?

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

Hemophilia A is caused due to deficiency of___________________?

A. Factor XI
B. Factor X
C. Factor IX
D. Factor VIII

Healing MCQs

Sideroblastic anemia is caused due to______________?

A. Lead
B. Mercury
C. Arsenic
D. Iron

Which of the following is not an example of massive splenomegaly ________________?

A. Chronic malaria
B. Chronic myeloid leukemia
C. Tropical splenomegaly
D. Acute lymphoblastic leukemia

Target cells are seen in peripheral blood in_______________?

A. Thalassemia
B. Aplastic anemia
C. Pernicious anemia
D. Sickle cell anemia

Schilling test is performed to find out______________?

A. Pancreatic enzyme deficiency
B. B12 malabsroption
C. Folic acid level
D. Coronary artery disease

Hemophilics show_________________?

A. Decreased bleeding time and clotting time
B. Increased bleeding time and clotting time
C. Decreased bleeding time and increased clotting time
D. Normal bleeding time and increased clotting time

Reed – Sternberg cells are seen in histopathological examination of_______________?

A. Burkitt’s lymphoma
B. Hodgkin’s disease
C. African jaw lymphoma
D. Infectious mononucleosis

Gingiva are enlarged in leukemia because of____________________?

A. Aplastic anaemia
B. Hemolytic anaemia
C. Hemophilia
D. Megaloblastic anemia

A patient with a bleeding disorder with increased bleeding time and normal clotting time is suffering from________________?

A. Christmas disease
B. Classic hemophilia
C. Vitamin K deficiency
D. Idiopathic thrombocytopenic purpura

The protein that carries iron from the gut to the body tissues is called________________?

A. Haemosiderin
B. Ferritin
C. Myoglobin
D. Transferrin

A 14 year old boy complains with gingival bleeding oral ulcers, anaemia with hepatomegaly but no lymphadenopathy, total eukocyte count of one-lakh cells per mm3 is suffering from________________?

A. Acute myeloid leukemia
B. Chronic lymphoblastic leukemia
C. Chronic monocytic leukemia
D. Chronic myeloid leukemia

Which of the following is not true for hemophilia A ________________?

A. In hemophilia A females are carriers
B. Hemophilia A is due to deficiency of factor VIII
C. Desmopressin is useful in the management of hemophilia A
D. Levels of factor VIII less than 50% are associated with spontaneous hemorrhage

Normal adult haemoglobin contains________________?

A. One alpha chains and two beta chains
B. One alpha chain and one beta chain
C. One beta chains and two alpha chains
D. Two alpha chains and two beta chains

Reduced number of platelet is found in all the conditions except____________________?

A. Aplastic anaemia
B. Disseminated intravascular coagulation
C. Acute myelocytic leukemia
D. Von willebrand disease

Chicken-wire appearance of enlarged bone marrow spaces is seen in_______________?

A. Haemophilia A
B. Sickle cell anaemia
C. Fetal alcohol syndrome
D. Beta thalassemia majon

Syndrome associated with increased risk of leukemia is_____________?

A. Sturge weber syndrome
B. Klinefelter syndrome
C. Plummer Vinson syndrome
D. Multiple hamartoma syndrome

Cell In Health And Diseases MCQs

Cooley’s anemia is also called___________________?

A. Beta – Thalassemia major
B. Mediterranean anemia
C. Erythroblastic anema
D. All of the above

In Troisiers sign the lymph nodes involved are_________________?

A. Left axillary nodes
B. Right axillary nodes
C. Right supraclavicular nodes
D. Left supraclavicular nodes

Thrombocytosis is seen in_______________?

A. DIsseminated intravascular coagulation
B. Osteopetrosis
C. Haemolytic anaemia
D. Thiazide therapy

The type of acute myelogenous leukemia associated with a high incidence of disseminated intravascular coagulation in________________?

A. Acute megakaryocytic leukaemia
B. Acute promyelocytic leukaemia
C. Acute erythroleukaemia
D. Acute myelomonocytic leukaemia

Lymphatic leukemoid reaction is usually seen in the following EXCEPT________________?

A. Pertussis
B. Tuberculosis
C. Lobar pneumonia
D. Viral infections

Amyloid material can be best diagnosed by___________________?

A. Polarized microscopy
B. X-ray crytallography
C. Electron microscopy
D. Scanning electron miscroscopy

Osteomalacia is associated with_________________?

A. Decrease in osteoid surface
B. Decrease in osteoid volume
C. Increase in osteoid maturation time
D. Increase in mineral apposition rate

All of the following causes excessive bleeding during tooth extraction except _______________?

A. Haemophilia – B
B. Haemophilia – A
C. Anti thrombin – III deficiency
D. Von-willebrand disease

All of the following can be transmitted through blood tranfusion except ______________?

A. Hepatitis
B. Leukemia
C. Malaria

Erythroblastosis fetalis is a condition seen when there is________________?

A. Rh +ve mother and Rh -ve foetus
B. Rh -ve mother and Rh +ve foetus
C. Rh -ve mother and Rh -ve foetus
D. Rh +ve mother and Rh +ve foetus

Aplastic anemia results from______________?

A. Whole body irradiation
B. Cytotoxic drugs
C. HIV infection
D. All of the above

Intrinsic factor for absorption of Vit B12 secreted in ______________?

A. Intestine
B. Stomach
C. Duodenum
D. Ileum

Pallor, spoon shaped nails, atrophic glossitis, with accompanied dysphagia is typical picture of ______________?

A. Plummer – Vinson syndrome
B. Vincent stomatitis
C. Trotters syndrome
D. None of the above

Increase in number of RBC is seen in ____________?

A. Leukemia
B. Neutropenia
C. Polycythemia
D. Anaemia

Hemophilia is best treated by _____________?

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

Torniquet test is function of________________?

A. Intrinsic pathway
B. capillary fragility
C. Platelet function
D. Extrinic pathway

Reliable screening test for hemophilia is_______________?


Normocytic, Normochromic anemia is seen in______________?

A. chronic disease
B. Hemolytic anemia
C. Acute blood loss
D. All of the above

Growth Disorders And Neoplasia MCQs

Which of the following is a hemolytic anemia________________?

A. Thalassemia
B. Sickle cell anemia
C. Hereditary spherocytosis
D. All of the above

Bence jones proteins are associated with__________________?

A. Burkitt’s lymphoma
B. Multiple myeloma
C. Hodgkin’s lymphoma
D. Infectious mononucleosis

In megaloblastic anaemia the cells are___________________?

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

In Hodgkin’s disease the lymphoa cells seen are__________________?

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

Which of the following is commonly involved in multiple myeloma_______________?

A. Pelvis
B. Vertebrae
C. Clavicle
D. Lungs

Hyper segmented neutrophils are seen in_________________?

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

Christmas disease is due to deficiency of________________?

A. Factor IX
B. Factor VIII
C. Factor X
D. Factor V

Both beta chains of haemoglobin are abnormal in_________________?

A. Homozygous sickle cell anemia
B. Thalassemia major
C. Heterozygous sickle cell trait
D. Megaloblastic anemia

In iron deficiency anemia there is_________________?

A. Decrease in hemoglobin
B. Increase in palatelets
C. Increase in hemoglobin
D. Decrease in platelets


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

In leucopenia, which cell type is predominantly involved ?

A. Eosinophils
B. Granulocytes
C. Erythrocytes
D. Monocytes

Gingiva are enlarged in leukemia because of__________________?

A. Erythrocyte engorgement
B. Capillary dilation
C. Edema
D. WBC infiltration

A patient reports with dyspnoea on slight exertion. He also has multiple petechial spots and spontaneous hemorrhage. His RBC count is less than one lakh/mm3 His hematocrit and hemoglobin is low. Most probable diagnosis is______________?

A. Thalassemia
B. Pernicious anemia
C. Aplastic anemia
D. Sprue

Pernicious anaemia is associated with the deficiency of________________?

A. Vitamin B1
B. Folic acid
C. Vitamin B6
D. Vitamin B12

In sickle cell anemia there is substitution of_________________?

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

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

A. Factor VIII concentrate
C. Cryoprecipitate
D. Platelet factor

A reduction in the total leucocyte count is called_________________?

A. Leucorrhoea
B. Leucopenia
C. Leucocytosis
D. Leukemia

Latest Medical MCQs – Competitive Diseases of Blood And Lymphnodes ( Pathology ) MCQs