PA_ WBC Disorders LE A 60 year old man with massive splenomegaly and progressive anemia, very high leucocyte

ocyte count and

18.2 Q left sided abdominal pain. Enumerate the differential diagnoses. Discuss the laboratory findings in any
one of them. (4+6)
PA_ WBC Disorders LE 65 year old male patient with painless generalized lymphadenopathy of a few years duration otherwise
18.2 Q asymptomatic was found to have a total leucocyte count of 50,000 cells/cumm with predominance of
lymphocytes. His platelet count was normal. What is the probable diagnosis? Discuss the blood and bone
marrow findings in this case.(2+8)
PA_ WBC Disorders LE 2 year old boy with a history of fever of one month duration was found to have hepatosplenomegaly,
18.2 Q petichiae, leucocyte count of 70,000cells/cumm and thrombocytopenia. What is your diagnosis? Discuss
the blood and bone marrow findings. Add a note on the recent classification of this disease. (2+6+2)
PA_ WBC Disorders LE A 25 year old female with a history of one month fever which is not responding to any antibiotics found
18.2 Q to have swollen bleeding gums, splenomegaly, petichiae and a very high leucocyte count. What is your
diagnosis? Discuss the WHO classification of this disease. Give the blood and bone marrow findings of
this disease. (2+3+5)
PA_ WBC Disorders LE A 55 year old male with left upper quadrant abdominal pain found to have massive splenomegaly, high
18.2 Q leucocyte count, anemia and normal platelet count. What is your diagnosis? Discuss the genetic basis of
this disease. Give the peripheral blood findings. (2+3+5)
PA_ WBC Disorders LE A 60 year old man with massive splenomegaly and progressive anemia, very high leucocyte count and
18.2 Q left sided abdominal pain. Enumerate the differential diagnoses. Discuss the laboratory findings in any
one of them. (4+6)
PA_ WBC Disorders LE 65 year old male patient with painless generalized lymphadenopathy of a few years duration otherwise
18.2 Q asymptomatic was found to have a total leucocyte count of 50,000 cells/cumm with predominance of
lymphocytes. His platelet count was normal. What is the probable diagnosis? Discuss the blood and bone
marrow findings in this case.(2+8)
PA_ WBC Disorders LE 2 year old boy with a history of fever of one month duration was found to have hepatosplenomegaly,
18.2 Q petichiae, leucocyte count of 70,000cells/cumm and thrombocytopenia. What is your diagnosis? Discuss
the blood and bone marrow findings. Add a note on the recent classification of this disease. (2+6+2)
PA_ WBC Disorders LE A 25 year old female with a history of one month fever which is not responding to any antibiotics found
18.2 Q to have swollen bleeding gums, splenomegaly, petichiae and a very high leucocyte count. What is your
diagnosis? Discuss the WHO classification of this disease. Give the blood and bone marrow findings of
this disease. (2+3+5)
PA_ WBC Disorders LE A 55 year old male with left upper quadrant abdominal pain found to have massive splenomegaly, high
18.2 Q leucocyte count, anemia and normal platelet count. What is your diagnosis? Discuss the genetic basis of
this disease. Give the peripheral blood findings. (2+3+5)
PA_ RBC Disorders LE 35 year old male patient who under went ileal resection 5 years back, got admitted now for evaluation of
15.2 Q anemia. Discuss the possible pathogenesis of his anemia and write the blood and bone marrow findings
in this case. (2+3+5)
PA_ RBC Disorders LE 75 year old man who under went partial gastrectomy five years back and was admitted for evaluation of
15.2 Q his anemia. Discuss the pathogenesis of his anemia. What will be the peripheral blood and bone marrow
findings in this case. (4+6)
PA_ RBC Disorders LE An 10 year old male complains of pain in the right upper abdomen. USG abdomen showed multiple gall
16.3 Q stones and absence of spleen. Give the hematological diagnosis?
PA_ RBC Disorders LE A 16-year-old female Gitika notices that her urinebecomes red after she was given sulfonamides. Name
16.3 Q the disese. Discuss the etiopathogenesis and laboratory diagnosis of the disease. (1+4+5)
PA_ Hemodynamic LE A 20 year old male sustained fracture of femur in a road traffic accident. On the 3 day of hospital stay he
6.5 Disorders Q suddenly developed respiratory distress and died. What is the probable diagnosis? Discuss the
pathogenesis and pathology of this condition (1+5+4)
PA_ Neoplasia S Write the differences between benign and malignant lesions
7.2 E
Q
PA_ Neoplasia S Enumerate Growth Factor Signalling pathways in oncogenesis
7.2 E
Q
PA_ Neoplasia S Tumor suppressor genes
7.2 E
Q
PA_ Neoplasia S Warburg effect
7.2 E
Q
PA_ Neoplasia LE List the oncogenic viruses. Describe the mechanism of carcinogenesis by Human Papilloma Virus (3+7)
7.3 Q
PA_ Neoplasia LE What are carcinogens? Mention the types of carcinogens. Discuss the role of viruses in carcinogenesis.
7.3 Q (2+3+5)
PA_ Neoplasia LE Classify chemical carcinogens. Describe the mechanism of chemical carcinogenesis (3+7)
7.3 Q
PA_ Neoplasia LE Define neoplasia. Classify tumors based on cell of origin. Discuss the difference between benign and
7.3 Q malignant tumors. (1+4+5)
PA_ Neoplasia LE Define neoplasm. Describe the the clinical, gross and microscopic features of malignant neoplasm
7.3 Q (1+3+3+3)
PA_ WBC Disorders LE Define leukemia. Write the WHO calssification of acute leukemias and discuss the blood and bone
18.2 Q marrow findings in Acute lymphoblastic leukemia (1+3+2+4)
PA_ WBC Disorders LE Define leukemia. Write the WHO calssification of acute leukemias and discuss the blood and bone
18.2 Q marrow findings in Acute myeloid leukemia (1+3+2+4)
PA_ WBC Disorders LE Enumerate the WBC's along with their normal reference range.Define Leucocytosis. Mention the causes
18.2 Q of increase in WBC's. (3+1+6)
PA_ WBC Disorders LE Define leukemia. Classify acute leukemias and discuss the blood and bone marrow findings in Acute
18.2 Q myeloid leukemia (1+3+2+4)
PA_ WBC Disorders LE Define leukemia. Write FAB classification of acute leukemias. Describe the blood and bone marrow
18.2 Q findings in acute myeloid leukemia. (2+3+2+3)
PA_ WBC Disorders LE Define and classify leukemias. Describe the etiopathogenesis and laboratory investigations in acute
18.2 Q myeloid leukemia (1+2+3+4)
PA_ WBC Disorders LE Define leukemia. Discuss the pathogenesis, phases of disease and peripheral blood findings in Chronic
18.2 Q myeloid leukemia (1+2+3+4)
PA_ WBC Disorders LE Define leukemia. Classify acute leukemias and discuss the blood and bone marrow findings in Acute
18.2 Q myeloid leukemia (1+3+2+4)
PA_ WBC Disorders LE Define leukemia. Write FAB classification of acute leukemias. Describe the blood and bone marrow
18.2 Q findings in acute myeloid leukemia. (2+3+5)
PA_ WBC Disorders LE Define and classify leukemias. Describe the etiopathogenesis and laboratory investigations in acute
18.2 Q myeloid leukemia (1+2+3+4)
PA_ WBC Disorders LE Define leukemia. Describe the blood and bone marrow findings in Acute lymphoblastic leukemia.
18.2 Q Enumerate the special stains that may help in differentiating acute myeloblastic leukemia from
lymphoblatic leukemia. (1+3+2+4)
PA_ WBC Disorders LE Define leukemia. Discuss the blood and bone marrow findings in Acute lymphoblastic leukemia.
18.2 Q Enumerate the differences between myeloblast and lymphoblast (1+2+4+3)
PA_ WBC Disorders LE Define , classify and mention the causes of Leukaemoid reactions. How do you differentiate with Chronic
18.2 Q Myeloid Leukamia (1+4+5)
PA_ WBC Disorders LE Define leukemia. Describe the blood and bone marrow findings in Acute lymphoblastic leukemia.
18.2 Q Enumerate the special stains that may help in differentiating acute myeloblastic leukemia from
lymphoblatic leukemia. (1+3+2+4)
PA_ WBC Disorders LE Define leukemia. Discuss the blood and bone marrow findings in Acute lymphoblastic leukemia.
18.2 Q Enumerate the differences between myeloblast and lymphoblast (1+2+4+3)
PA_ WBC Disorders LE Define leukemia. Write the WHO calssification of acute leukemias and discuss the blood and bone
18.2 Q marrow findings in Acute lymphoblastic leukemia (1+3+2+4)
PA_ WBC Disorders LE Define leukemia. Write the WHO calssification of acute leukemias and discuss the blood and bone
18.2 Q marrow findings in Acute myeloid leukemia (1+3+2+4)
PA_ WBC Disorders LE Define leukemia. Discuss the pathogenesis, phases of disease and peripheral blood findings in Chronic
18.2 Q myeloid leukemia (1+2+3+4)
PA_ WBC Disorders LE Write the WHO classification of lymphomas. Discuss the blood and bone marrow findings in CLL. (5+3+2)
18.2 Q
PA_ Inflammation LE Define wound healing. Describe mechanism & morphology of cutaneous wound healing. Mention factors
5.1 Q affecting wound healing.(1+3+3+3)
PA_ Inflammation LE Describe hematopoesis and its regulation with a labelled diagram. List the causes for extramedullary
13.1 Q hematopoesis (3+2+5)
PA_ RBC Disorders LE Classify anemia. Discuss the investigations in anemia. (5+5)
13.2 Q
PA_ RBC Disorders LE Describe the laboratory approach to a case of anemia? Correlate the peripheral blood smear findings
13.5 Q with RBC indices in a case of anemia (5+5)
PA_ RBC Disorders LE Discuss iron metabolism. Describe the peripheral blood findings in iron deficiency anemia. (5+5)
14.1 Q
PA_ RBC Disorders LE Define anemia. Give the differential diagnosis of microcytic hypochromic anemia. Discuss the laboratory
14.1 Q investigation of microcytic hypochromic anemias? (2+3+5)
PA_ RBC Disorders LE Define anemia. Enumerate causes Iron deficiency. Discuss the laboratory investigation of Iron deficiency
14.2 Q anemia? (2+4+4)
PA_ RBC Disorders LE Define anemia. Enumerate causes for macrocytosis. Discuss the laboratory investigation of megaloblastic
15.1 Q anemia? (2+3+5)
PA_ RBC Disorders LE Describe the etiopathogenesis and lab investigations of megaloblastic anemia (5+5)
15.1 Q
PA_ RBC Disorders LE Define anemia. Enumerate causes for megaloblastic anemia. Discuss the laboratory investigation of
15.1 Q Pernicious anemia? (2+3)
PA_ RBC Disorders LE Define and classify hemolytic anemia, Describe the laboratory investigations of hemolytic anemia (1+3+6)
16.1 Q
PA_ RBC Disorders LE Define and classify hemolytic anemia ,Describe the laboratory findings in Thalesimia (1+3+6)
16.1 Q
PA_ RBC Disorders LE Define haemolytic anemias, classify and Describe the laboratory approach to hemolytic anemia (1+3+6)
16.1 Q
PA_ RBC Disorders LE Classify thalassemia, Describe etiopathogenesis and the laboratory findings of beta thallesemia (1+3+6)
16.1 Q
PA_ RBC Disorders LE Define haemolytic anemias. Classify and describe the etiology, pathogenesis, and peripheral blood
16.1 Q picture of Acquired hemolytic anemia (1+1+3+3+2)
PA_ RBC Disorders LE Describe the etiopathogenesis and laboratory diagnosis of sickle cell anemia (5+5)
16.3 Q
PA_ RBC Disorders LE Describe the etiopathogenesis and laboratory diagnosis of HEREDITRAY SPHEROCYTOSIS (5+5)
16.3 Q
PA_ WBC Disorders LE Define and classify plasma cell dyscrasias. Describe the lab inestigations in multiple myeloma.
20.1 Q
PA_ Inflammation LE Define inflammation. Mention the types of inflammation. Describe the Vascular events of inflammation
4.1 Q (2+2+6)
PA_ Inflammation LE Define inflammation. Describe Cellular events of inflammation (2+8)
4.1 Q
PA_ Inflammation LE Define inflammation. Describe role of Chemical mediators of inflammation (2+8)
4.2 Q
PA_ Hemodynamic LE Define Oedema. Enumerate the causes for edema. Describe pathogenesis of Renal edema. (1+4+5)
6.1 Disorders Q
PA_ Hemodynamic LE Define Oedema. Enumerate the causes for edema. Describe pathogenesis of cardiac edema. (1+4+5)
6.1 Disorders Q
PA_ Hemodynamic LE Define and classify Shock. Describe the pathogenesis of septic shock (1+3+6)
6.3 Disorders Q
PA_ Hemodynamic LE Define Thrombosis. Describe the etiopathogenesis, morphology and fate of thrombus (1+3+3+3)
6.4 Disorders Q
PA_ Hemodynamic LE Define thombosis. Discuss Virchow's triad. Describe the fate of thrombus (1+5+4)
6.4 Disorders Q
PA_ Hemodynamic LE Define embolism. Mention different types of emboli and discuss the pathogenesis and morphology of fat
6.5 Disorders Q embolism (1+3+3+3)
PA_ Infectious disease, S A 45 year old man presented in a dermatology OPD with hypopigmented anesthetic patch on his face.
10.3 Amyloidosis, E O/E peripheral nerves were thickened. a) What is your diagnosis? Â b) What are the investigations you
nutritional and Q want to do in this case? Â c) Describe the etiopathogenesis and morphology of this disease?
environmental
diseases
PA_ Diseases of immune S Define hypersensitivity reaction. Classify with examples
9.2 system E
Q
PA_ Diseases of immune S Define hypersensitivity reaction. Describe type IV hypersensitivity reaction
9.2 system E
Q
PA_ Infectious disease, S Describe the pathogenesis of health disorders due to air pollution (2+3)
12.1 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ Infectious disease, S Describe the pathogenesis of health disorders due to tobacco usage (2+3)
12.1 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ Infectious disease, S Describe the pathogenesis of health disorders due to alcohol (2+3)
12.1 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ Infectious disease, S Describe the pathogenesis of disorders caused by protein calorie malnutrition (2+3)
12.1 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ Infectious disease, S Describe the pathogenesis of disorders caused by starvation (2+3)
12.2 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ Infectious disease, S Describe the pathogenesis of obesity and its consequence (2+3)
12.3 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ Cellular Responses to S What is oxidative stress? Describe the pathomechanism of reactive oxygen species induced cell injury.
2.1 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Define necrosis and mention types of necrosis. Describe morphology of two types of necrosis with
2.4 Stress and Toxic E examples
Insults Q
PA_ Hemorrhagic S Enumerate the causes of thrombocytopenia. Describe the clinical features, invsetigations and prognosis
21.2 diathesis E of idiopathic thrombocytopenic purpura.
Q
PA_ Hemorrhagic S Describe the etiopathogenesis, complications and lab investigations in DIC.
21.4 diathesis E
Q
PA_ Blood banking and S Name four blood group systems. Describe in detail about principle of inheritance of ABO blood group
22.1 basic diagnostic E with a note on bombay blood group system.
cytology Q
PA_ Blood banking and S Discuss the preparation and uses of cell block technique.
8.3 basic diagnostic E
cytology Q
PA_ Diseases of immune S Definehypersensitivity reaction. Describe type II hypersensitivity reaction
9.2 system E
Q
PA_ WBC Disorders S Define Leukaemoid reaction. Classify them and write the features of any one
18.1 E
Q
PA_ WBC Disorders S Define Neutropenia and Neutrophilia. List out the causes of Neutrophilia and Neutropenia
18.1 E
Q
PA_ WBC Disorders S Define Eosinopenia and Eosinophilia. List out the causes of Eosinopenia and Eosinophilia
18.1 E
Q
PA_ WBC Disorders S Define Lymphopenia and Lymphocytosis. List out the causes of Lymphopenia and Lymphocytosis
18.1 E
Q
PA_ WBC Disorders S Classify AML based on genetic abnormalities
18.2 E
Q
PA_ WBC Disorders S What is Philadelphia chromosome. Describe the translocation seen in it. List TWO conditions where it is
18.2 E seen (1+2+2)
Q
PA_ Inflammation S Discuss differences between exudate and transudate
4.1 E
Q
PA_ Inflammation S Discuss the role of Phagocytosis in health and disease
4.1 E
Q
PA_ Inflammation S what is granulation tissue? Write the microscopy of Granulation Tissue with a labelled diagram.(1+4)
5.1 E
Q
PA_ Inflammation S Describe healing of fracture .
5.1 E
Q
PA_ Inflammation S Define Stem cell and describe its role in health and disease (1+2+2)
5.1 E
Q
PA_ Infectious disease, S Describe the etiopathogenesis and morphology of Cerebral malaria
10.1 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ Infectious disease, S Describe the etiopathogenesis and morphology of Secondary tuberculosis
10.3 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ Infectious disease, S Describe the pathogenesis and morphology of Cysticercosis
10.4 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ RBC Disorders S Describe the etiopathogenesis and lab diagnosis of Paroxysmal Nocturnal Hemoglobinuria
14.1 E
Q
PA_ RBC Disorders S classify and Describe the etiopathogenesis of hemolytic anemia
14.1 E
Q
PA_ RBC Disorders S Describe the laboratory findings in hemolytic anemia
14.1 E
Q
PA_ RBC Disorders S Describe the pathogenesis and lab diagnosis of sickle cell anemia
14.2 E
Q
PA_ RBC Disorders S Describe the pathogenesis and lab diagnosisof thallasemia
14.2 E
Q
PA_ RBC Disorders S Describe the etiopathogenesis and lab diagnosis of heriditary spherocytosis
14.2 E
Q
PA_ RBC Disorders S Describe the etiopathogenesis and laboratory diagnosis of G6PD deficiency
14.2 E
Q
PA_ RBC Disorders S Describe the etiopathogenesis and lab diagnosis Immune hemolytic anemia
14.3 E
Q
PA_ RBC Disorders S Discuss Vitamin A defeciency
15.1 E
Q
PA_ RBC Disorders S Write THREE complications of Lead toxicity.Detail about clinical features and lab investigations in lead
15.1 E toxicity.
Q
PA_ RBC Disorders S Describe the mechanism of action and use of various anticoagulants in pathology
15.2 E
Q
PA_ RBC Disorders S Discuss Hazards of smoking
15.2 E
Q
PA_ RBC Disorders S Discuss adverse effects of Alcohol
15.2 E
Q
PA_ RBC Disorders S Describe Obesity associated disease
15.2 E
Q
PA_ RBC Disorders S write classification of vitamins and Describe the METABOLISM and morphology of Vitamin A deficiency
15.2 E
Q
PA_ RBC Disorders S Describe the laboratory approach to a case of anemia
15.3 E
Q
PA_ RBC Disorders S Describe hematopoesis and its regulation with a labelled diagram
15.4 E
Q
PA_ RBC Disorders S Define microcytic hypochromic anemia . Its causes and Give the differential diagnosis for microcytic
16.3 E hypochromic anemia.
Q
PA_ RBC Disorders S List THREE Indications for bone marrow aspiration and biopsy . Describe the findings of bone marrow
16.1 E aspiration in megaloblastic anemia
Q
PA_ RBC Disorders S Define anemia. Classification of hemolytic anemia.List causes and peripheral blood picture of
16.2 E microangiopathic hemolytic anemia
Q
PA_ RBC Disorders S Describe laboratory investigations of macrocytic anemia
16.2 E
Q
PA_ RBC Disorders S Describe the etiopathogenesis of MACROCYTIC anemia
16.3 E
Q
PA_ RBC Disorders S Compare the laboratory findings in differential diagnosis of microcytic hypochromic anemia
16.3 E
Q
PA_ RBC Disorders S Describe the laboratory findings in microcytic hypochromic anemia
16.3 E
Q
PA_ RBC Disorders S Discuss in detail of iron metabolism. Draw a diagram of Peripheral blood picture in Iron deficiency
16.3 E anemia
Q
PA_ RBC Disorders S Differentiate megaloblastic anemia and non megaloblastic anemia based on etiopathogenic and
16.3 E laboratory findings
Q
PA_ RBC Disorders S list causes of macrocytic anemia, its differential diagnosis and peripheral blood smear picture of
16.3 E macrocytic anemia
Q
PA_ RBC Disorders S Define and classify Thalassemia. Discuss pathogenesis of thalassemia.
16.3 E
Q
PA_ RBC Disorders S Mention Membrane defects in RBCs.Add a note on Hereditary spherocytosis
16.3 E
Q
PA_ RBC Disorders S mention causes ofHemolytic anemia of newborn.Discuss lab investigations in hemolytic anemias
16.3 E
Q
PA_ RBC Disorders S Describe factors influencing severity of sickle cell anemia. Add a note on Clinical features of sickle cell
16.3 E anemia .
Q
PA_ RBC Disorders S How do you investigate a case of aplastic anemia?
16.3 E
Q
PA_ RBC Disorders S Write iron profile findings in Microcytic anemia. Diagram of peripheral blood picture in microcytic
16.4 E anemia
Q
PA_ RBC Disorders S Mention the Bone marrow picture in megaloblastic anemia.Discuss Lab diagnosis of megaloblastic
16.4 E anemia
Q
PA_ RBC Disorders S Describe clinical features of sickle cell disease. List tests for sickling
16.4 E
Q
PA_ RBC Disorders S List THREE important features of hemolytic disease of new born due to ABO incompatibility. Write lab
16.4 E investigations in hemolytic disease
Q
PA_ RBC Disorders S Clasify hemolytic anemia and draw a pheripheral picture of haemolytic anemia
16.4 E
Q
PA_ RBC Disorders S Describe Laboratory findings in pernicious anemia.
16.5 E
Q
PA_ Cellular Responses to S Describe Oxygen derived free radicals induced cell injury
2.1 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe Pathogenic mechanism in irreversible Cell injury
2.2 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe the pathogenesis of Reperfusion injury
2.2 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Explain the mechanism of fatty change of liver in chronic alcoholism
2.3 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Classify Pigments. Describe Exogenous pigments in health and diseases(1+4)
2.3 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe the etiopathogenesis and morphology of Fatty change (3+2)
2.3 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Discuss Endogenous pigment in health and disease (2+3)
2.3 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Define and classify Necrosis. Describe the fat necrosis (1+1+3)
2.4 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe the etiopathogenesis and morphology of Caseous Necrosis (3+2)
2.4 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Define and classify Necrosis. Describe the caseous necrosis (1+1+3)
2.4 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe the etiopathogenesis and morphology of Coagulative Necrosis (3+2)
2.4 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe the etiopathogenesis and morphology of Gangrene (3+2)
2.5 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Define and classify Necrosis .Describe the gross and microscopy of Gas Gangrene(1+1+3)
2.5 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe the etiopathogenesis and morphology of Pathologic Calcification (3+2)
2.5 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe Atrophy in health & Diseases with examples (2+3)
2.6 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe hyperplasia in health and diseases with examples (2+3)
2.6 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Define dysplasia. Describe its significance with examples (1+4)
2.6 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Describe hypertrophy in health and diseases with examples (2+3)
2.6 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S Define Metaplasia. Describe the different types of metaplasia with examples (1+4)
2.6 Stress and Toxic E
Insults Q
PA_ Cellular Responses to S What are Telomeres and what is their function in ageing and cancer? (1+2+2)
2.7 Stress and Toxic E
Insults Q
PA_ WBC Disorders S Define Bence Jones proteinuria? Describe the method of detecting them. Name two causes of Bence
20.1 E Jones Proteinuria (1+3+1)
Q
PA_ Blood banking and S List out the blood components prepared in Blood Bank. Mention the indications of any one of them (2+3)
22.2 basic diagnostic E
cytology Q
PA_ Blood banking and S Classify Transfusion reactions. Mention the steps followed in investigating a transfusion reaction.
22.2 basic diagnostic E
cytology Q
PA_ Infectious disease, S Describe the etiopathogenesis and morphology of amyloidosis (2+3)
3.1 Amyloidosis, E
nutritional and Q
environmental
diseases
PA_ Inflammation S What are the cardinal signs of inflammation? Discuss their pathologic basis (2+3)
4.1 E
Q
PA_ Inflammation S Define inflammation. Describe the vasuclar events in inflammation (1+4)
4.1 E
Q
PA_ Inflammation S Define chemotaxis and discuss the mechanism of Chemotaxis (1+4)
4.2 E
Q
PA_ Inflammation S Discuss the role of chemical mediators in inflammation
4.2 E
Q
PA_ Inflammation S Describe the role of Cytokines in inflammation.
4.2 E
Q
PA_ Inflammation S Define inflammation. Describe the cellular events in inflammation(1+4)
4.3 E
Q
PA_ Inflammation S Describe role of macrophage in chronic inflammation
4.3 E
Q
PA_ Inflammation S Define granuloma and describe the mechanism of formation of granuloma. (2+3)
4.3 E
Q
PA_ Inflammation S Define & Classify Granuloma. Write neat labelled diagram of Granuloma (1+2+2)
4.3 E
Q
PA_ Inflammation S Draw a neat diagram of caseating granuloma and name condition associated with caseating granulomas
4.4 E (4+1)
Q
PA_ Inflammation S Define inflammation. Describe the microscopic features of acute inflammation (1+4)
4.4 E
Q
PA_ Hemodynamic S Describe the mechanisms of cardiac edema
6.1 Disorders E
Q
PA_ Hemodynamic S Describe the mechanisms of Renal edema
6.1 Disorders E
Q
PA_ Hemodynamic S What is the mechanism behind the nut meg appearance of liver in chronic venous congestion
6.2 Disorders E
Q
PA_ Hemodynamic S Describe the etiopathogenesis and morphology of of chronic venous congestion of lung.(3+2)
6.2 Disorders E
Q
PA_ Hemodynamic S Describe the etiopathogenesis and morphology of chronic venous congestion of spleen.(3+2)
6.2 Disorders E
Q
PA_ Hemodynamic S Define and classfy Shock. Describe etiopathogenesis of cardiogenenic shock.(1+2+2)
6.3 Disorders E
Q
PA_ Hemodynamic S Discuss the pathogenesis of septic shock
6.3 Disorders E
Q
PA_ Hemodynamic S Enumerate the components of Virchow's triad. Discuss their role in thrombogenesis (1+4)
6.4 Disorders E
Q
PA_ Hemodynamic S Discuss the mechanism and morphology of Amniotic fluid embolism (3+2)
6.5 Disorders E
Q
PA_ Hemodynamic S Discuss the mechanism and morphology of Fat embolism (3+2)
6.5 Disorders E
Q
PA_ Neoplasia S Describe the mechanism and pathways of spread of malignant tumors.
7.1 E
Q
PA_ Neoplasia S Discuss the morphologic and molecular changes in Adenoma-Carcinoma sequence (2+3)
7.1 E
Q
PA_ Neoplasia S Discuss the role of p53 in tumorigenesis.
7.2 E
Q
PA_ Neoplasia S What are oncogenes? Describe their role in tumorogenesis.
7.2 E
Q
PA_ Neoplasia S Write five differences between initiators and promotors of carcinogenesis
7.3 E
Q
PA_ Neoplasia S Discuss the role of viruses in carcinogenesis.
7.3 E
Q
PA_ Neoplasia S Describe the mechanism of Chemical carcinogenesis.
7.3 E
Q
PA_ Neoplasia S Describe the role of Tumor markers in the diagnosis and management of cancer patients.
7.4 E
Q
PA_ Neoplasia S Discuss the laboratory diagnosis of cancers.
7.4 E
Q
PA_ Neoplasia S What are Paraneoplastic syndromes? Discuss their pathogenesis.
7.4 E
Q
PA_ Blood banking and S Discuss technique, indications and findings in cervical pap smear
8.2 basic diagnostic E
cytology Q
PA_ Blood banking and S Discuss advantages and disadvantages of Frozen section
8.2 basic diagnostic E
cytology Q
PA_ Diseases of immune S Describe the etiopathogenesis and morphology of Type-I hypersensitivity reaction (3+2)
9.2 system E
Q
PA_ Diseases of immune S Describe the mechanism of Type-III hypersensitivity reaction with an example
9.2 system E
Q
PA_ Diseases of immune S Describe the etiopathogenesis and morphology of Graft versus host disease
9.3 system E
Q
PA_ Diseases of immune S Describe the etiopathogenesis and morphology of Graft rejection
9.3 system E
Q
PA_ Diseases of immune S Discuss the role of HLA system in health & disease
9.3 system E
Q
PA_ Diseases of immune S List primary immunodeficiency diseases and discuss Di George syndrome
9.3 system E
Q
PA_ Diseases of immune S List primary immunodeficiency diseases and discuss Chronic granulomatous disease
9.3 system E
Q
AETC AETCOM S Describe Autonomy, Beneficence and Non-maleficence
OM_ E
2.2 Q
AETC AETCOM S Define patient autonomy and contrast atonomy with paternalism
OM_ E
2.5 Q
PA_ Diseases of immune S Define hypersensitivity reaction. Describe type I hypersensitivity reaction
9.2 system E
Q