MCQs of Oral Pathology & Medicine – Diseases of Blood

All of the following statements about idiopathic thrombocytopenic purpura are true EXCEPT:

The oral findings in erythroblastosis fetalis include:

The red blood cells in beta thalassemia are typically:

Hair-on-end appearance in a skull roentgenogram is seen in:

Which of the following is not a finding in classical hemophilia (hemophilia A):

Neurological symptoms and premature graying of hair is associated with:

Which of the following is seen in idiopathic thrombocytopenic purpura:

Which of the following disease is known as the Kissing disease

To prevent excessive bleeding during surgery a patient with hemophilia A may be given:

Hemophilia B is due to:

Paul Bunnell test is positive in:

A young patient is hospitalized with petechiae of oral mucous membrane, marginal gingival hemorrhage and with a platelet count of 45,000/ cc The BT and Clot Retraction time are increased, RBC and TLC are normal He is suffering from:

Pinpoint hemorrhages of < 1cm diameter are known as:

Which of the following agents is of value in the postoperative care of the hemophilic patient?

Pernicious anemia is:

Which of the following is not associated with haemorrhage?

Necrotising ragged ulceration with no apparent inflammatory response is indicative of:

Leucocytopenia is seen in:

Bleeding time is prolonged in:

Clinical features of infectious mononucleosis

Petechial hemorrhage is seen in:

Christmas disease is due to deficiency of:

A boy complains of bleeding gums, swollen, joints with hemorrhage into joints His paternal and maternal uncle complains of same problem It is due to deficiency of factor:

Common oral change seen with nutritional anemia is:

Hypopigmentation, gray streaks of hair, degranulation defect of neutrophils and neuropathy are seen in:

Chronic granulocytic leukemia is due to:

Bleeding joints is a characteristic feature of:

Plummer – vinson syndrome:

Patient giving history of thrombocytopenic purpura reports for extraction What could be the most common postoperative complication:

For extraction in a leukemic patient:

All of the following statements about acute leukemia in children are true except:

Which of the following is the most serious and life threatening blood dyscrasias caused with a drug:

Monospot test is used to diagnose:

Precancerous potential in plummer-vinson’s syndrome may be due to change in the epithelium like:

Infectious mononucleosis has:

Chemotherapy can be successful during treatment of:

Virus responsible for infectious mononucleosis is:

Oral manifestations of infectious mononucleosis is most commonly:

megaloblastic anaemia occurs due to:

One of the following syndrome is characterized by an esophageal web with resulting dysphagia, atrophic changes in the mucous membranes of the mouth and a hypochromic microcytic anemia

Aplastic anaemia is common with:

Hemophilia is associated with:

Which of the following is sex linked disorder?

A hair on end appearance of the skull is seen in all of the following except:

A patient on warfarin sodium following myocardial infarction reports for an oral surgical procedure which one of the following laboratory tests should be preferred to ascertain the fitness:

Which of the following is not true about thalassemia?

Erythroblastosis fetalis can be prevented if the mother is injected at parturition, with an antibody called:

Deficiency of all the three components of coagulation factor VIII result in:

Cooley’s anemia is also known as:

The most striking haematological finding in agranulocytosis is:

The most common coagulation disorders haemophilia A and von Willebrand’s disease are due to:

In Radionucide imaging the most useful radio pharmaceutical for skeletal imaging is:

The most reliable criteria in Gustafson’s method of identification is:

Which of the following blood disease has a racial predilection?

All the following are TRUE in Immune thrombocytopenic Purpura (ITP) EXCEPT:

Chediak- Higashi syndrome is inherited as:

Commonest mode of inheritance of Von Willebrand’s disease is: