Internal Medicine/ Hematology
- Basics of Hematology.
- Hematology.***) The majority of hemoglobin in erythrocytes from the normal adults is termed:
- Hemoglobin F
- Hemoglobin A
- Hemoglobin A2
- Hemoglobin C
- Hemoglobin Bart'sAnswer: B* Hemoglobin A***) Platelets normally have a half life of:
- 7 minutes
- 7 hours
- 7 days
- 4 weeks
- 3 monthsAnswer: C* 7 days***) In human being, normal red blood cell survival time is approximately:
- One month
- 80 Days
- Three months
- 120 days
- Five monthsAnswer: D* 120 days***) All the following are true concerning lymphocytes, except:
- Are formed in the spleen
- Enters the circulation via lymphatics
- Are the precursors of platelets
- Are reduced in number by immunosuppressive therapy
- Are more sensitive to irradiation than granulocytesAnswer: C* Are the precursors of platelets***) Phagocytosis is a primary function of:
- Neutrophils
- Monocytes
- Lymphocytes
- Eosinophiles
- ErythrocytesAnswer: A* Neutrophils
- Erythrocyte Sedimentation Rate (ESR).***) All of the following may cause very high ESR, except:
- Active rheumatoid arthritis
- Giant cell arteritis
- Sickle cell anemia
- Carcinomatosis
- Multiple myelomaAnswer: C* Sickle cell anemia
- Common Presentations.
- Skin Pigmentation Disorders.***) Generalized increased pigmentation may be seen in all of the following, except:
- Hypopituitarism
- Chronic liver disease
- Addison disease
- Hemochromatosis
- Ectopic ACTH secretionAnswer: A* Hypopituitarism***) Generalized increased pigmentation may be seen in all of the following, except:
- Nelson's syndrome
- Hemochromatosis
- Chronic renal failure
- Panhypopituitarism
- Primary biliary cirrhosisAnswer: D* Panhypopituitarism***) All of the following are known causes of hypopigmentation except:
- Albinism
- Tuberous sclerosis
- Post inflammatory
- Addison disease
- VitiligoAnswer: D* Addison disease
- Palmar Erythema.***) All of the following can cause palmar erythema, except:
- Epilepsy
- Alcoholism
- Rheumatoid arthritis
- Pregnancy
- PolycythemiaAnswer: A* Epilepsy***) All of the following can cause palmar erythema, except:
- Rheumatoid arthritis
- Pregnancy
- Thyrotoxicosis
- Multiple sclerosis
- Liver cirrhosisAnswer: D* Multiple sclerosis
- Splenomegaly.***) Splenomegaly is expected to be present in all of the following, except:
- Glucose-6-phosphate dehydrogenase deficiency
- Congenital spherocytosis
- Hemoglobin H disease
- Pyruvate kinase deficiency
- Chronic immune hemolytic anemiaAnswer: A* Glucose-6-phosphate dehydrogenase deficiency***) Splenomegaly can occur in all of the following, except:
- Celiac disease
- Portal hypertension
- Tuberculosis
- Sarcoidosis
- Infectious mononucleosisAnswer: A* Celiac disease***) Splenomegaly can occur in all of the following, except:
- Celiac disease
- Myelofibrosis
- Kala azar
- Typhoid fever
- EndocarditisAnswer: A* Celiac disease***) Splenomegaly can occur in all of the following, except:
- Thalassemia
- Portal hypertension
- Celiac disease
- Early in sickle cell anemia
- Leishmaniasis (Kala-azar)Answer: C* Celiac disease***) Splenomegaly can occur in all of the following, except:
- Chronic granulocytic leukemia
- Chronic malaria
- Amyloidosis
- Celiac disease
- BrucellosisAnswer: D* Celiac disease
- Lymphadenopathy.***) Generalized lymphadenopathy is seen in all of the following, except:
- Sarcoidosis
- Hepatic cirrhosis
- Lymphoma
- HIV infection
- Infectious mononucleosisAnswer: B* Hepatic cirrhosis***) All of the following are causes of cervical lymph node enlargement, except:
- Infectious mononucleosis
- Toxoplasmosis
- Anemia
- Tuberculosis
- Rheumatic feverAnswer: C* Anemia***) All of the following are causes of cervical lymph node enlargement, except:
- Multiple myeloma
- Sarcoidosis
- Tuberculosis
- Chronic lymphoid leukemia
- PhenytoinAnswer: A* Multiple myeloma
- Polycythemia.***) All of the following may produce polycythemia, except:
- Cushing’s syndrome
- Primary hepatoma
- Heavy smoking
- Gastric carcinoma
- High altitudesAnswer: D* Gastric carcinoma***) All of the following may produce polycythemia, except:
- Hepatoma
- Right to the left shunt
- Hematoma
- Multiple myeloma
- Fibroma of uterusAnswer: D* Multiple myeloma***) All of the following are causes of polycythemia, except:
- High altitude
- Right to left shunt
- Lymphoma
- Massive uterine fibroma
- Renal cell carcinomaAnswer: C* Lymphoma
- Thrombocytopenia.***) Thrombocytopenia caused by increased platelet destruction is most closely associated with which of the following:
- Aplastic anemia
- Acute leukemia
- Combination chemotherapy
- Systemic lupus erythematosus SLE
- Excessive ethanol uptakeAnswer: E* Excessive ethanol uptake***) Causes of thrombocytopenia include all of the following, except:
- Aplastic anemia
- Pernicious anemia
- Polycythemia rubra vera
- Hypersplenism
- Disseminated intravascular coagulationAnswer: C* Polycythemia Rubra Vera***) Which of the following laboratory procedure can detect thrombocytopenia:
- Clotting time
- Prothrombin time
- Bleeding time
- Partial thromboplastin time
- Thrombin timeAnswer: C* Bleeding time
- Pancytopenia.***) All of the following can cause pancytopenia, except: Q2012
- Leukemoid reaction
- Aplastic anemia
- Hypersplenism
- Myelofibrosis
- Megaloblastic anemiaAnswer: A* Leukemoid reaction***) All of the following can cause pancytopenia, except:
- Aplastic anemia
- Megaloblastic anemia
- Iron deficiency anemia
- Hypersplenism
- Systemic lupus erythematosusAnswer: C* Iron deficiency anemia***) All of the following are causes of pancytopenia, except:
- Hereditary spherocytosis
- Aplastic anemia
- Megaloblastic anemia
- Hypersplenism
- MyelofibrosisAnswer: A* Hereditary spherocytosis
- Neutrophilia.***) All of the following are causes of neutrophil leucocytosis, except:
- Bacterial infection
- Myocardial infarction
- Viral infection
- Leukemia
- Leukemoid reactionAnswer: C* Viral infection***) Leucocytosis may occur in all of the following, except:
- Brucellosis
- Myocardial infarction
- Bacterial infection
- Burns
- InfancyAnswer: E* Infancy
- Neutropenia.***) All of the following are causes of neutropenia, except:
- Viral infections
- Felty's syndrome
- Typhoid fever
- Myocardial infarction
- CongenitalAnswer: D* Myocardial infarction***) Which of the following is not a recognized cause of neutropenia:
- Multiple myeloma
- Corticosteroids
- Cytotoxic drugs
- Typhoid fever
- Felty's syndromeAnswer: B* Corticosteroids***) Neutropenia is least likely to be caused by one of the following:
- Cytotoxic therapy
- Bone marrow transplant
- Radiotherapy
- Diabetic ketoacidosis
- Splenic enlargementAnswer: D* Diabetic ketoacidosis
- Eosinophilia.***) Which of the following would be least likely to be associated with eosinophilia: Q2012
- Asthma
- Contact dermatitis
- Parasitic infection
- Mycobacterial infection
- Prednisone administrationAnswer: E* Prednisone administration***) Which of the following would be least likely to be associated with eosinophilia:
- Toxoplasmosis
- Hypoadrenocorticism
- Loeffler's endocarditis
- Allergic vasculitis
- MyxedemaAnswer: E* Myxedema
- Microcytic Anemia.
- Microcytic Anemia.***) Which of the following may be a cause of microcytosis:
- Vitamin B12 deficiency
- Folic acid deficiency
- Beta-thalassemia
- Reticulocytosis
- Aplastic anemiaAnswer: C* Beta-thalassemia***) Which of the following would be most likely to be a cause of hypochromic microcytic anemia:
- Thalassemia
- Immune hemolytic anemia
- Methotrexate therapy
- Obstructive jaundice
- Phenytoin therapyAnswer: A* Thalassemia***) Microcytic anemia can be caused by all of the following, except:
- Iron deficiency
- Anemia of chronic disease
- Thalassemia
- Sideroblastic anemia
- Folate deficiencyAnswer: E* Folate deficiency***) Microcytic hypochromic anemia is associated with all except:
- Thalassemia
- Iron deficiency anemia
- Vitamin B12 deficiency
- Chronic infection
- Lead poisoningAnswer: C* Vitamin B12 deficiency***) Microcytic hypochromic blood picture is seen in all of the following, except:
- Iron deficiency anemia
- Lead poisoning
- Thalassemia
- Sideroblastic anemia
- Sickle cell anemiaAnswer: E* Sickle cell anemia
- Iron Metabolism.***) All of the following increase iron absorption in the small intestine, except:
- Increased acidity
- When iron is complemented with lactose
- Ascorbic acid
- Tea drinking
- Iron of animal sourceAnswer: D* Tea drinking***) All of the following about iron are true, except:
- Ferrous iron absorbed better than ferric
- Iron absorption takes place in the terminal ileum
- The average daily iron intake is 10-20 mg
- Alcohol increases iron absorption
- Iron deficiency is the commonest anemiaAnswer: B* Iron absorption takes place in the terminal ileum
- Iron Deficiency Anemia.***) All of the following about iron deficiency anemia are true, except:
- Is the commonest type of anemia in Jordan
- May occur during pregnancy
- Stomatitis may occur
- Treatment of choice is intravenous iron
- Causes microcytosis with hypochromiaAnswer: D* Treatment of choice is intravenous iron***) In iron deficiency anemia which of the following is true:
- Serum binding capacity is decreased
- Marrow iron stores are normal
- Sideroblasts in the marrow are increased
- Serum iron concentration is decreased
- Tear drop cells on blood filmAnswer: D* Serum iron concentration is decreased***) In a patient with anemia all of the following might suggest the presence of iron deficiency anemia, except:
- Microcytosis
- Koilonychia
- Peripheral neuropathy
- High iron binding capacity
- Low serum ferritinAnswer: C* Peripheral neuropathy***) The appropriate treatment of iron deficient anemia is:
- Just encourage red meat in the diet
- Iron and vitamins must be supplemented
- Elemental iron is mandatory at a dose of 4-6 mg/kg/day orally
- Blood transfusion to supply RBSs as well as iron
- Injectable ironAnswer: C* Elemental iron is mandatory at a dose of 4-6 mg/kg/day orally
- Normocytic Anemia.
- Aplastic Anemia.***) All of the following are causes of aplastic anemia, except:
- Fanconi's anemia
- Benzene
- Insecticides
- Viral hepatitis
- MeningitisAnswer: E* Meningitis***) Aplastic anemia may occur following the administration of which of the following:
- Penicillin
- Prednisolone
- Tetracycline
- Chloramphenicol
- ErythromycinAnswer: D* Chloramphenicol
- Hemolytic Anemia.
- Hemolytic Anemia.***) Hemolysis may occur in all of the following, except:
- Hereditary spherocytosis
- Aplastic anemia
- Thalassemia
- Sickle cell anemia
- Glucose-6-phosphate deficiencyAnswer: B* Aplastic anemia***) All of the following are hemolytic anemias, except:
- Hereditary spherocytosis
- Hereditary elliptocytosis
- G-6-PD deficiency
- Sickle cell anemia
- Aplastic anemiaAnswer: E* Aplastic anemia***) The presence of hemolysis is indicated by all of the following clinical manifestations, except:
- Present or reduced serum haptoglobin
- Increased number of reticulocytes
- Elevated serum lactate dehydrogenase
- Microcytic red blood cell indices
- Shortened red blood cell survivalAnswer: D* Microcytic red blood cell indices***) The hemolytic anemia is associated with the following, except:
- Increased indirect bilirubin
- Decreased haptoglobin
- Increased reticulocytes count
- Decreased free hemoglobin
- Increased PCVAnswer: D* Decreased free hemoglobin***) The following are characteristic of hemolytic type of jaundice, except:
- Increased serum unconjugated bilirubin
- Bilirubin does not appear in the urine
- Abnormal liver function tests
- Increased urinary urobilinogen
- AnemiaAnswer: C* Abnormal liver function tests
- Thalassemia.***) All of the following are features of thalassemia, except: Q2012
- Bone marrow hyperplasia
- Hair on end appearance
- Hypochromic microcytic RBCs
- Increased osmotic fragility
- SplenomegalyAnswer: D* Increased osmotic fragility***) All of the following are acquired anemia, except:
- Iron-deficiency anemia
- Megaloblastic anemia
- Aplastic anemia
- Thalassemia
- Auto-immune hemolytic anemiaAnswer: D* Thalassemia***) One of the following is not true of Beta-thalassemia trait (minor):
- Mild anemia is usually present
- Spleen is usually palpable
- Peripheral smear is usually abnormal
- Mean corpuscular volume is usually low
- Hemoglobin A2 is usually elevatedAnswer: B* Spleen is usually palpable***) Beta-thalassemia (major) usually manifests at the age of:
- Newborn period
- 4 months
- 8 months
- 12 months
- 24 monthsAnswer: C* 8 months***) Concerning Thalassemia major, all the following are true, except:
- Hemolytic anemia resulting from imbalance of alpha and beta globin chains
- Patient becomes symptomatic in the second 6 months
- Facial deformities are present from expansion of the bone marrow
- Splenomegaly is present after 2 years from presentation
- Hypochromic microcytic anemiaAnswer: D* Splenomegaly is present after 2 years from presentation***) All of the following are features of Beta-thalassemia major, except:
- Skull X-ray show "hair on end" appearance
- Blood film shows hypochromic and microcytic picture
- It is usually asymptomatic
- Hepatosplenomegaly is a feature
- It is inherited diseaseAnswer: C* It is usually asymptomatic***) In the treatment of thalassemia syndromes which of the following is true:
- Splenectomy is contraindicated in thalassemia major
- Transfusion is unnecessary if the hemoglobin remains above 10 g/dl
- Small iron supplements are beneficial even in the absence of iron deficiency anemia
- The level of fetal hemoglobin is 2-5% during the first year of life
- Immunization with pneumococcal polysaccharide vaccine is not recommendedAnswer: B* Transfusion is unnecessary if the hemoglobin remains above 10 g/dl
- Sickle Cell Disease.***) All of the following about sickle cell anemia are true, except:
- More common in black
- Increased incidence of salmonella osteomyelitis
- Predisposes to auto-splenectomy
- More susceptible to falciparum malaria
- Sickle cell tract are usually asymptomaticAnswer: D* More susceptible to falciparum malaria***) The following features may be found in an adult with sickle cell anemia, except:
- Aseptic necrosis of bone
- Massive splenomegaly
- Chronic leg ulcers
- Hematuria
- Impaired ability to concentrate urineAnswer: B* Massive splenomegaly***) All can be associated with Sickle Cell Anemia, except:
- Vaso-occlusive crisis
- Infection
- Bleeding disease
- Organ damage
- Chest SyndromeAnswer: C* Bleeding disease
- G6PD Deficiency.***) All the following are oxidant stress which can cause hemolysis in patient with Glucose-6-phosphate dehydrogenase (G6PD) deficiency, except:
- Infection
- Sulfa drugs
- Vit E
- Fava beans
- NitrofurantoinAnswer: C* Vit E***) Favism is a hemolytic anemia caused by deficiency of:
- Pyruvate kinase
- Glucose-6-phosphate dehydrogenase
- Al-antitrypsin
- Alanine aminotransferase
- Acid phosphataseAnswer: B* Glucose-6-phosphate dehydrogenase
- Macrocytic Anemia.
- Vitamin B12 Deficiency.***) All of the following are features of pernicious anemia, except:
- Usually over 30 years, with blue eyes
- Microcytic and hypochromic anemia
- Subacute combined degeneration of the cord can occur
- Dementia is a feature
- Optic atrophy can occurAnswer: B* Microcytic and hypochromic anemia***) All of the following about pernicious anemia are true, except:
- Is a disease of elderly
- Weight loss is a common feature
- Subacute combined degeneration can occur
- Gastric atrophy with achlorhydria
- Treatment should be continued for two yearsAnswer: E* Treatment should be continued for two years***) All of the following are causes of macrocytic anemia, except: Q2012
- Vit B12 deficiency
- Folate deficiency
- Hypothyroidism
- Hyperthyroidism
- Chronic liver diseaseAnswer: D* Hyperthyroidism***) A macrocytic peripheral blood smear may be seen in any of the following, except:
- Alcoholism
- Hypothyroidism
- Celiac disease
- Folate deficiency
- Iron deficiencyAnswer: E* Iron deficiency***) All of the following are causes of macrocytic anemia, except:
- Vit B12 deficiency
- Chronic liver disease
- Sickle cell anemia
- Hypothyroidism
- Folate deficiencyAnswer: C* Sickle cell anemia***) All of the following are causes of macrocytosis (large red cells), except:
- Alcoholism
- Hypothyroidism
- Chronic renal failure
- Sideroblastic anemia
- HemolysisAnswer: D* Sideroblastic anemia***) All about vitamin B12 are true, except:
- It is a cobalt containing substance
- Deficiency causes large primitive red cell precursors to appear in the peripheral blood
- It is mainly absorbed in terminal ileum
- It is bound firmly to intrinsic factor prior to absorption
- It presents in high amount of vegetablesAnswer: E* It presents in high amount of vegetables
- Folate Deficiency.***) Megaloblastic anemia secondary to folate deficiency is best corrected by administering folate:
- Intravenously 10 mg daily
- Intramuscularly 1 gm daily
- Orally 5 mg daily
- Subcutaneously 100 mg monthly
- In combination with ascorbic acidAnswer: C* Orally 5 mg daily***) Which of the following statements about megaloblastic anemia is not true:
- Serum folic acid and vitamin B12 may be normal
- Manifestation may appear in the first year of life
- White blood cells and platelets are normal
- Occasionally treatment is required for life
- In Jordan goat's milk may be a factor in its etiologyAnswer: A* Serum folic acid and vitamin B12 may be normal
- Hemostasis.
- Hemostasis.***) A boy bleeding a lot after circumcision may have any of the following, except:
- Factor XIII deficiency
- Factor XII deficiency
- Factor XI deficiency
- Factor X deficiency
- Factor IX deficiencyAnswer: B* Factor XII deficiency***) In vascular injury the immediate response that produce hemostasis is:
- Platelet adherence at the injury site
- Vasoconstriction
- Liberation of serotonin
- Thrombus formation
- Platelet plug formationAnswer: B* Vasoconstriction
- Heparin-Induced Thrombocytopenia.***) Anticoagulant effect of heparin is based on: Q2012
- Alteration of thrombin levels
- Potentiation of antithrombin III
- Activation of plasmin into plasminogen
- Inactivation of ionized calcium
- Reduction of available factor VIIAnswer: B* Potentiation of antithrombin III***) With anti-coagulant (heparin) therapy the antidote treatment of choice is: Q2012
- Calcium gluconate
- Protamine sulfate
- Potassium chloride
- Vitamin K
- Cetrovorum factorAnswer: B* Protamine sulfate***) The most useful test in monitoring heparin therapy is:
- Bleeding time
- Prothrombin time
- Platelet aggregation
- Clot retraction
- Partial thromboplastin time (PTT)Answer: E* Partial thromboplastin time (PTT)***) Important uses of acetylsalicylic acid include all of the following, except:
- Acute rheumatic fever
- Antipyretic
- Thrombocytopenia
- Transient ischemic attacks
- Mild migraine headacheAnswer: C* Thrombocytopenia***) Which of the following drugs should not be given together:
- Streptomycin and INH
- Penicillin and gentamycin
- Warfarin and aspirin
- Glycosides and metformin
- Vitamin B12 and folic acidAnswer: C* Warfarin and aspirin***) Contraindications to the use of streptokinase therapy include all of the following, except:
- Bleeding peptic ulcer
- Infective endocarditis
- Surgery to eye
- Cor pulmonale
- Severe hepatic insufficiencyAnswer: D* Cor pulmonale
- Vitamin K Deficiency.***) The most frequent and clinically important vitamin deficiency developing in patients with cholestatic liver disease is which of the following:
- Vitamin D
- Vitamin A
- Vitamin B12
- Vitamin Bl
- Vitamin KAnswer: E* Vitamin K***) Vitamin K dependent coagulation factors may include all the following, except:
- Factor 2
- Factor 7
- Factor 9
- Factor 11
- Factor 10Answer: D* Factor 11
- Disseminated Intravascular Coagulation.***) All of the following can cause disseminated intravascular coagulation, except:
- Gram negative septicemia
- Von Willebrand's disease
- Falciparum malaria
- Snake bites
- SurgeryAnswer: B* Von Willebrand's disease
- Neoplasms.
- Polycythemia Rubra Vera.***) Polycythemia Rubra Vera is associated with all of the following, except:
- Raised ESR
- Pruritus
- Hemorrhage
- Hyperuricemia
- ThrombosisAnswer: A* Raised ESR
- Acute Lymphoblastic Leukemia.***) Concerning acute lymphocytic leukemia all of the following are true, except:
- Most patients will have anemia
- Most patients will have thrombocytopenia
- Spleen is generally not enlarged
- Leukemic lymphocytes in blood smear are present
- Bone marrow is essential for the diagnosisAnswer: C* Spleen is generally not enlarged
- Lymphoma.***) Which of the following tumors has a strong association with a viral infection:
- Acute lymphoblastic leukemia
- Acute myelogenous leukemia
- Histiocytosis
- Burkitt's lymphoma
- Hodgkin's diseaseAnswer: D* Burkitt's lymphoma
- Hodgkin Lymphoma.***) Concerning Hodgkin's lymphoma all of the following are correct, except:
- It occurs in both males and females but more in males
- It occurs in children and old ages
- Histologically it is multi-cellular infiltration with a characteristic giant cells
- It starts usually in extra-nodal tissues
- Radiotherapy forms the main line of treatment in early stagesAnswer: D* It starts usually in extra-nodal tissues***) All the following are histological subtype of Hodgkin's lymphoma except:
- Lymphocyte predominant
- Lymphocyte depleted
- Mixed cellularity
- Nodular sclerosis
- Leukemic lymphocytic predominantAnswer: E* Leukemic lymphocytic predominant
- Multiple Myeloma.***) The following are features of multiple myeloma, except: Q2012
- Renal failure
- Hypocalcemia
- Lytic bone lesions
- Anemia
- M-band on protein electrophoresisAnswer: B* Hypocalcemia***) All of the following about multiple myeloma is correct, except:
- It is a disease of elderly
- Backache is a common symptom
- Renal failure can occur
- The ESR is usually slightly elevated
- Bence-Jones protein is present in urineAnswer: D* The ESR is usually slightly elevated***) All of the following about multiple myeloma are true, except:
- Backache
- Recurrent infections
- May cause hypercalcemia
- Presence of Bence-Jones protein in urine
- High alkaline phosphataseAnswer: E* High alkaline phosphatase***) The following are features of multiple myeloma, except:
- Bone pain
- Hypercalcemia
- Renal failure
- Bleeding tendency
- PolycythemiaAnswer: E* Polycythemia
- Blood Products and Transfusions.
- Blood Products.***) Plasma from group-A blood will agglutinate:
- Only group AB blood
- Only group B blood
- Group B blood and group AB blood
- Group AB blood, and group O blood
- Group B blood and group O bloodAnswer: C* Group B blood and group AB blood
- Platelets.***) The most helpful and reliable bedside platelet function is:
- Platelet adhesiveness
- Bleeding time
- Clot retraction
- Platelet size
- Clotting timeAnswer: B* Bleeding time
- Coagulation Factors.***) To stop bleeding in hemophilic baby you have to give:
- Fibrinogen
- Albumin
- Fresh frozen plasma
- Cryoprecipitate
- Platelet rich plasmaAnswer: D* Cryoprecipitate***) The liver is the sole site of synthesis of all of the following coagulation factors, except:
- Factor II
- Factor V
- Factor VII
- Factor IX
- Factor IVAnswer: E* Factor IV***) Stored blood is deficient in:
- Factor 2
- Factor 7
- Factor 8
- Factor 9
- Factor 10Answer: C* Factor 8
- Blood Transfusion.***) All of the following are complications of blood transfusion, except: Q2012
- Hypothermia
- Hypocalcemia
- Hyperkalemia
- Thrombocytopenia
- ThromboembolismAnswer: E* Thromboembolism***) All of the following are complications of blood transfusion, except:
- Hypercalcemia
- Hemolytic reactions
- Anaphylactic reactions
- Hepatitis C
- HIV infectionAnswer: A* Hypercalcemia***) In massive blood transfusion, all the following are complication except:
- Acute congestive heart failure
- Transmission of infection
- Transfusion reaction
- Hypercalcemia
- HyperkalemiaAnswer: D* Hypercalcemia***) All of the following are potential risks of massive blood transfusion, except:
- Acidosis
- Impaired hemostasis
- Hypokalemia
- Citrate toxicity
- Impaired oxygen deliveryAnswer: C* Hypokalemia***) All the following are possible complications of blood transfusion except:
- Hypercalcemia
- Congestive cardiac failure
- Hyperkalemia
- Incompatibility
- Non-cardiogenic pulmonary edemaAnswer: A* Hypercalcemia***) The most fatal complication of blood transfusion is:
- Allergic reactions
- Anaphylactic reaction
- Human error
- Bacterial contamination
- Pyrogenic reactionAnswer: C* Human error***) All the following diseases are transmitted through blood transfusion except:
- Syphilis
- Helicobacter Pylori
- Malaria
- Hepatitis B and C
- Epstein-Bar virusAnswer: B* Helicobacter Pylori
- Immunosuppressive Drugs.
- Steroids.***) Prolonged use of corticosteroids may cause the following, except: Q2012
- Proximal myopathy
- Metabolic alkalosis
- Avascular necrosis of the head femur
- Thrombocytopenia
- LeukocytosisAnswer: D* Thrombocytopenia***) The following complicate steroid therapy, except:
- Hyperglycemia
- Osteoporosis
- Hyperkalemia
- Skin atrophy
- Weight gainAnswer: C* Hyperkalemia***) All of the following are side effects of steroids, except:
- Cataract
- Retardation of growth in children
- Increased incidence of vascular thrombosis
- Hyperglycemia
- OsteoporosisAnswer: C* Increased incidence of vascular thrombosis***) All of the following are side effects of corticosteroids, except:
- Hypertension
- Peptic ulcer disease
- Hyperkalemia
- Osteoporosis
- AcneAnswer: C* Hyperkalemia***) All of the following are side effects of long term steroid therapy, except:
- Osteoporosis
- Hypertension
- Hematuria
- Diabetes mellitus
- Delayed healing of woundsAnswer: C* Hematuria***) Prolonged use of corticosteroids may cause the following, except:
- Adrenocortical suppression
- Skin malignancy
- A papulopustular facial rash
- Purpura
- Cutaneous striaeAnswer: B* Skin malignancy***) Corticosteroids could be used in the treatment of all the following, except:
- Acute leukemia
- Nephrotic syndrome
- Sydenham's chorea
- Rheumatoid iridocyclitis
- Addison's diseaseAnswer: C* Sydenham's chorea
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