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Questions For Phase 2 MBBS General Pathology
Questions For Phase 2 MBBS General Pathology
Long Questions
Necrosis , types and examples, fate of necrosed area, difference between apoptosis and
necrosis
Define apoptosis, what are the cause of apoptosis. Write about the biochemical features and
mechanisms of apoptosis. Add a note on deregulated apoptosis
Types of degeneration, pathology of organ affected by fatty changes, add a note on fat
stains
Short Questions
Write about cell injury and write briefly about hyperplasia with suitable examples
Cellular swelling
Necrosis
Gangrenous necrosis
Fat necrosis
Tissue necrosis- Morphological patterns
Caseous necrosis
Definition and characteristic of types of necrosis
Free radical cell injury
Morphological changes in apoptosis
Mechanism of apoptosis
Classify pigments and write about lipofuscins
Hemosiderin deposits in the diseases
Difference between the dysplastic and metastatic calcification
Write about dystrophic and metastatic calcifications
Pathological calcification
Metastatic calcification
Define hyperplasia and give two examples
Define atrophy. Give two examples to physiological atrophy
Mention 4 nuclear changes in necrosis
Types of necrosis with examples
Enumerate four examples for metastatic calcification
Enlist two common stains used to demonstrate fat in tissues
INFLAMMATION
Long Questions
Long Questions
Long Questions
Short Questions
Long Questions
Define auto, iso, allo , xenografts, factors influencing allograft rejection, types and
mechanism of allograft rejection
Classify primary immunodeficiency syndrome, details about AIDS
Short Questions
Long Questions
Classify neoplasia, difference between benign and malignant tumor, mode of spread of
malignant tumor
Metastasis, different pathway of spread , details about anyone
Write in detail about carcinogenesis physical, chemical and biological and also molecular
basis of carcinogenesis
Define neoplasia, discuss in detail the pathogenesis and pathophysiology of radiation
oncogenesis
Mention oncogenic viruses. Describe oncogenesis by HPV
Short Questions
Tumor markers
Teratoma
Growth factors
Chemical carcinogen
Hamartoma
Carcinoma in situ
Paraneoplastic syndrome
FNAC
Laboratory diagnosis of cancer
Difference between benign and malignant tumors
Metaplasia
Dysplasia
Tumor metastasis
Tumor suppressor genes
Oncogenic RNA virus
Grading and staging of tumor
Automatic tissue processor
Differentiation and anaplasia
Trans coelomic spread of neoplasm
Molecular basis of cancer
P53
Tumor antigens
EBV
Lab diagnosis of neoplasm
Exfoliative cytology
Liquid base cytology
Define metaplasia and give 2 examples
Warburg effect
Two tumor suppressor genes
Name four virus implicated in carcinogenesis
INFECTIOUS DISEASE
Long Questions
Short Questions
PEM
Kwashiorkor
Vitamin A deficiency
Rickets
Vit D deficiency
Obesity
Lead poisoning
Vitamin C deficiency
Give two examples for trace elements and their deficiency states
Mention two causes for Basophilic Stippling
Gross skeletal changes in rickets
INFANCY AND CHILDHOOD
Short Questions
Long Questions
Classify hemolytic anemia, compare etiopathogenesis and lab findings of Thalassemia and
sickle cell anemia
Classify Hemolytic anemia, write in detail about the pathogenesis, Blood picture and clinical
features of Beta Thalassemia Major
How will you interpret bone marrow, bone marrow findings of megaloblastic anemia
Classify anemia, details about iron deficiency anemia
Classify thrombocytopenia, etiopathogenesis, details about idiopathic thrombocytopenic
purpura
Define Thrombocytopenia? Classify causes of thrombocytopenia? Discuss the various test in
evaluating bleeding disorders?
Short Questions
Reticulocyte
Evidences of haemolytic anemia
PCV estimation and its significance
Hematocrit
G6PD deficiency anemia
Sickle cell disease
Pathogenesis of sickle cell disease
Peripheral blood smear and bone marrow changes in Vitamin B12 deficiency (Megaloblastic
anemia ) (6)
Coomb’s test
Bone marrow changes in microcytic anemia
Microcytic hypochromic anemia
Etiology and morphology of bone marrow in Aplastic Anemia
Pancytopenia in peripheral smear
Aplastic anemia
Fanconi’s anemia
Polycythemia Vera
Prothrombin time
Bleeding time
Thrombocytopenia
Chronic ITP
Idiopathic thrombocytopenic purpura
Hemolytic Uremic Syndrome
Glanzmann’s disease
Coagulation disorders
Mention Important investigations necessary for diagnosis of Hemophilia
hemophilia A
Von Willebrand’s disease
Christmas disease
DIC
Pathogenesis of DIC
DIC lab diagnosis
Transfusion reaction
Complications of blood transfusion
Sideroblastic anemia
Osmotic fragility test
Indication of bone marrow aspiration
Laboratory Investigations done for diagnosis of Autoimmune Haemolytic Anaemia
What are red cell indices ?
MCV
Mention 4 applications of reticulocyte count
Heinz Bodies
Reticulocyte
Howell-jolly body
Tests for Sickling
Coomb’s test
Megaloblast
Mention two important marrow changes in B12 deficiency
Blood picture in Megaloblastic anemia
Give 4 causes for IDA
Mention two causes of pancytopenia
Prothrombin time
Mention the causes of Thrombocytopenia
Bernard Soulier syndrome
Hemophilia
What is cross matching?
What is Bombay Blood group?
Sea blue histiocytes
Mention 4 indications of Bone marrow aspiration
Cross matching
Blood components prepared in a blood bank
WBC DISORDERS
Long Questions
40 years male H/o chronic fatigue, weight loss since 6 months. O/E pallor, marked
splenomegaly+, laboratory report shows Hb 10 GM%, TC 215000/CMM. Platelets 4
lacks/mm. Answer the following: a) What is your diagnosis? b) What is common genetic
abnormality? c) Blood and Bone Marrow findings to confirm your diagnosis? d) Prognosis of
the condition?
A 70 year old women admitted with worsening anemia and pathological fracture of the
Humerus had an ESR of 120mm in 1 hour. Her peripheral smear showed increased rouleaux
formation. X-ray of skull showed multiple punched out osteolytic lesions. a) What is the most
probable diagnosis? Write briefly on the etiopathogenesis of this disease. b) Describe the
Bone Marrow Changes in this disease. c) Enumerate the common laboratory investigations
for this disease. d. Enlist the complications of this disease.
40 yrs female c/o loss of weight, huge splenomegaly with peripheral blood white blood cell
count of more than 1 lakh cells/cc a) What is the probable diagnosis? b) What are the
characteristic peripheral smear findings? c) What is the course of the disease? d) What is
the chromosomal abnormality involved?
60 yrs male presented with normocytic normochromic anaemia, pathological fracture femur
and proteinuria. X ray skull revealed punched out lesions in the calvarium and peripheral
smear studied show rouleaux formation. a) What is your probable diagnosis. b) Discuss in
detail the molecular pathogenesis, morphology and clinical features of above said disorder.
23 yrs female presented with oral ulcers, malar rash photosensitivity and non erosive arthritis
involving both knees. Laboratory investigations show persistent proteinuria and leucopenia.
What is your probable diagnosis.
40 yr old male presented with h/o fever, vomiting and diarrhoea. Patient had temperature of
103 degrees F. Weak rapid pulse, hypotension, tachypnea, cold, clammy, cyanotic skin.
Blood culture gram negative bacterial infection positive. a) What is your diagnosis? b)
Explain the pathogenesis and morphology.