🇮🇳 AIIMS PG (DM/MCh) Entrance · flashcards

AIIMS PG (DM/MCh) Entrance Pathology, Microbiology and Laboratory Medicine Flashcards

56 question-and-answer cards covering Pathology, Microbiology and Laboratory Medicine as it is examined in AIIMS PG (DM/MCh) Entrance. 24 of them are printed below, taken from across the deck — no signup, no paywall on the preview.

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24 sample cards from the Pathology, Microbiology and Laboratory Medicine deck

Sampled from the end of the deck, so these are different cards from the ones shown on the syllabus page.

  1. What is the diagnostic cell of Hodgkin lymphoma and its immunophenotype?

    Reed-Sternberg cell — a large binucleate ('owl-eye') cell, classically CD15-positive and CD30-positive, CD45-negative, CD20-negative (classical HL).

  2. Which translocation and oncogene characterize Burkitt lymphoma, and what is the histologic appearance?

    t(8;14) juxtaposing MYC to the IgH locus. 'Starry sky' appearance from tingible-body macrophages amid a sea of monomorphic intermediate B cells; very high proliferation (Ki-67 ~100%).

  3. What defines multiple myeloma diagnostically (CRAB criteria)?

    CRAB: hyperCalcemia, Renal insufficiency, Anemia, Bone lytic lesions. Plus clonal plasma cells ≥10% in marrow, M-protein (monoclonal spike), Bence-Jones proteinuria, and rouleaux on smear.

  4. Describe the coagulation cascade's intrinsic vs extrinsic pathway and the tests that assess each.

    Intrinsic pathway (factors XII, XI, IX, VIII) assessed by aPTT. Extrinsic pathway (factor VII + tissue factor) assessed by PT/INR. Common pathway (X, V, II, fibrinogen) affects both.

  5. Differentiate Hemophilia A from von Willebrand disease in terms of deficiency and lab findings.

    Hemophilia A: factor VIII deficiency, X-linked, prolonged aPTT, normal bleeding time/platelets. von Willebrand disease: vWF deficiency, autosomal, prolonged aPTT and bleeding time, abnormal ristocetin aggregation; most common inherited bleeding disorder.

  6. What are the major ABO blood group compatibility rules for RBC transfusion?

    Type O is universal RBC donor (no A/B antigens); type AB is universal RBC recipient (no anti-A/anti-B antibodies). For plasma, AB is universal donor and O is universal recipient (reverse of RBC).

  7. Distinguish acute hemolytic transfusion reaction from febrile non-hemolytic reaction.

    Acute hemolytic: ABO incompatibility, complement-mediated intravascular hemolysis, fever, flank pain, hemoglobinuria, DIC, shock — a medical emergency. Febrile non-hemolytic: most common, from recipient antibodies to donor leukocytes/cytokines, fever and chills without hemolysis.

  8. Give the Gram stain mechanism and classify Staphylococcus vs Streptococcus on catalase.

    Gram-positive bacteria retain crystal violet (thick peptidoglycan, stain purple); gram-negative lose it and take safranin (pink). Staphylococcus is catalase-positive; Streptococcus is catalase-negative.

  9. How is Staphylococcus aureus distinguished from coagulase-negative staphylococci, and what test identifies it?

    S. aureus is coagulase-positive (and DNase/mannitol-fermenting on MSA, golden colonies). Coagulase-negative staphylococci (S. epidermidis, S. saprophyticus) are coagulase-negative; S. saprophyticus is novobiocin-resistant.

  10. Classify streptococci by hemolysis and Lancefield grouping with key species.

    Alpha-hemolytic (green): S. pneumoniae (optochin-sensitive, bile-soluble), viridans (resistant). Beta-hemolytic: Group A S. pyogenes (bacitracin-sensitive), Group B S. agalactiae (CAMP-positive). Gamma (non-hemolytic): Enterococcus.

  11. What is the mechanism of action of the diphtheria and cholera toxins (ADP-ribosylation targets)?

    Diphtheria toxin ADP-ribosylates elongation factor 2 (EF-2), halting protein synthesis. Cholera toxin ADP-ribosylates Gs (stimulatory G protein), permanently activating adenylate cyclase, raising cAMP and causing watery diarrhea.

  12. Which acid-fast organism causes tuberculosis and what stain identifies it?

    Mycobacterium tuberculosis, identified by the Ziehl-Neelsen (acid-fast) stain due to mycolic acid in its cell wall; auramine-rhodamine fluorescent stain is more sensitive for screening.

  13. Describe the Baltimore classification basis and give an example of a positive-sense ssRNA virus.

    The Baltimore system classifies viruses by genome type and mRNA synthesis strategy (I dsDNA, II ssDNA, III dsRNA, IV +ssRNA, V -ssRNA, VI ssRNA-RT, VII dsDNA-RT). Example of +ssRNA: poliovirus, hepatitis C, SARS-CoV-2.

  14. Interpret the hepatitis B serology pattern: HBsAg+, anti-HBc IgM+, HBeAg+.

    Acute hepatitis B infection with high infectivity. HBsAg = active infection; anti-HBc IgM = recent/acute; HBeAg = active viral replication and high transmissibility. (Anti-HBs alone = immunity/vaccination.)

  15. Which malaria species causes the most severe disease and relapse, respectively, and why?

    P. falciparum causes the most severe disease (cerebral malaria, high parasitemia, no hypnozoites). P. vivax and P. ovale cause relapses due to dormant liver hypnozoites (treated with primaquine).

  16. Name the dimorphic fungi and the diagnostic India ink finding for Cryptococcus.

    Dimorphic fungi (mold in cold/environment, yeast at 37°C in body): Histoplasma, Blastomyces, Coccidioides, Paracoccidioides, Sporothrix. Cryptococcus neoformans shows a halo (clear capsule) around yeast on India ink prep of CSF.

  17. Classify the four Gell and Coombs hypersensitivity reactions with one example each.

    Type I (IgE/immediate — anaphylaxis, atopy); Type II (antibody-mediated cytotoxic — autoimmune hemolytic anemia, Goodpasture); Type III (immune complex — SLE, serum sickness); Type IV (delayed cell-mediated/T cell — TB skin test, contact dermatitis).

  18. What is the gold-standard surveillance metric for hospital-acquired infection control and a key prevention bundle?

    Surgical site infection and device-associated infection rates (CLABSI, CAUTI, VAP) per 1000 device-days. Hand hygiene (WHO 5 moments) is the single most effective measure; central-line bundles prevent CLABSI.

  19. Differentiate the Papanicolaou (Pap) stain components and the Bethesda system's purpose.

    Pap stain: hematoxylin (nuclei blue), with OG-6 and EA cytoplasmic counterstains showing transparency for cell overlap. The Bethesda system standardizes cervical cytology reporting (e.g., ASC-US, LSIL, HSIL) including specimen adequacy.

  20. What fixative is standard for histopathology and what is the principle of immunohistochemistry?

    10% neutral buffered formalin (cross-links proteins via methylene bridges) is the standard fixative. IHC uses labeled antibodies (with chromogen like DAB) to detect specific tissue antigens, localizing protein expression in situ.

  21. Explain the principle of PCR and the key role of Taq polymerase.

    Polymerase chain reaction exponentially amplifies a target DNA sequence through repeated cycles of denaturation (~95°C), primer annealing (~50-65°C), and extension (~72°C). Taq, a thermostable polymerase from Thermus aquaticus, survives denaturation temperatures.

  22. What does the Ct (cycle threshold) value indicate in real-time quantitative PCR?

    Ct is the cycle number at which fluorescent signal crosses the detection threshold; it is inversely proportional to the starting target nucleic acid amount (lower Ct = higher initial template/viral load).

  23. Define the components and purpose of a Westgard rule and a Levey-Jennings chart in lab QC.

    A Levey-Jennings chart plots control results against mean ± SD over time. Westgard multirules (e.g., 1-3s, 2-2s, R-4s, 1-2s warning) detect random and systematic error to flag out-of-control runs before reporting patient results.

  24. What are the four biosafety levels (BSL) and an example organism handled at BSL-3?

    BSL-1 (non-pathogenic, e.g., E. coli K-12), BSL-2 (moderate, e.g., Staph, Salmonella, HBV), BSL-3 (serious airborne, e.g., Mycobacterium tuberculosis, SARS-CoV-2), BSL-4 (lethal, no treatment, e.g., Ebola, Marburg) requiring maximum containment.

What this deck covers

The Pathology, Microbiology and Laboratory Medicine deck follows the AIIMS PG (DM/MCh) Entrance Pathology, Microbiology and Laboratory Medicine syllabus — 4 chapters and 14 topics — so questions land on material that is genuinely examinable rather than trivia around it. That works out to roughly 14.0 cards per chapter.

Answers are written to be recallable, not just readable — averaging about 217 characters, which is long enough to carry the reasoning and short enough to say out loud.

A deck like this earns its keep on the second and third pass. Read the syllabus first so you know the shape of the subject, then use the cards to find the specific facts that have not stuck.

Pathology, Microbiology and Laboratory Medicine flashcards FAQ

How many Pathology, Microbiology and Laboratory Medicine flashcards are in this AIIMS PG (DM/MCh) Entrance deck?

56 cards. This page previews 24 of them, sampled evenly across the deck so you can judge the difficulty before installing anything.

Are these AIIMS PG (DM/MCh) Entrance flashcards free?

Yes. The preview here is free to read with no signup, and the full 56-card deck is free inside the Examius app.

What do the Pathology, Microbiology and Laboratory Medicine cards cover?

They follow the AIIMS PG (DM/MCh) Entrance Pathology, Microbiology and Laboratory Medicine syllabus — 4 chapters and 14 topics — so the questions track what is actually examinable.

How should I use these flashcards?

Read the syllabus first so you know the shape of the subject, then drill the deck. Examius schedules each card with spaced repetition, so cards you keep missing come back sooner and ones you know drift further apart.