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IST Internal Assignment 3 - Cytology (2024 Batch) - Model Answers


CASE 1

A 55-year-old diabetic male with fever and right thigh swelling of 1 week duration. Single swelling 4×3 cm, firm, mobile, tender, erythematous with local rise of temperature. FNA done.

Q1. What is the Diagnosis?

Acute Pyogenic Abscess (Soft Tissue Abscess of the Thigh)
The clinical features - diabetes (predisposing to bacterial infections), fever, a tender, erythematous, warm swelling of 1 week duration - point to an acute pyogenic abscess.

Q2. Describe the Slide Findings

The FNA smear from a pyogenic abscess typically shows:
  1. Background - turbid/creamy aspirate; smear background shows necrotic debris and proteinaceous material
  2. Inflammatory cells - large numbers of degenerated and intact neutrophils (pus cells) - the hallmark finding
  3. Macrophages/histiocytes - scattered, with engulfed cellular debris (phagocytosis)
  4. Cellular debris - abundant necrotic material in the background
  5. Absence of epithelial cell clusters or granulomas - distinguishes it from carcinoma or tuberculosis
  6. Bacteria - may be visible (Gram stain shows cocci or bacilli depending on causative organism)
  7. Red blood cells - scattered in background
Note for the diabetic patient: Staphylococcus aureus is the most common causative organism of soft tissue abscesses; in diabetics, consider also Gram-negative organisms and anaerobes. Culture and sensitivity of aspirated pus is mandatory.


CASE 2

A 55-year-old female with blood-stained vaginal discharge. PAP Smear: Squamous cells with large hyperchromatic irregular nuclei, tadpole cells, neutrophils, necrotic debris in the background.

Q1. What is the Diagnosis?

Squamous Cell Carcinoma (SCC) of the Uterine Cervix
The Pap smear features are classical for invasive squamous cell carcinoma:
  • Large hyperchromatic irregular nuclei (malignant nuclear features)
  • Tadpole cells - elongated tumor cells with a broad head and tapering tail; pathognomonic of keratinising SCC
  • Tumor diathesis background (neutrophils + necrotic debris) indicating invasion through tissue

Q2. Aetiology of this Condition

The primary aetiology is Human Papillomavirus (HPV) infection, particularly:
  • High-risk oncogenic types: HPV 16 and HPV 18 together account for ~70% of all cervical cancers
  • Other high-risk types: HPV 31, 33, 45, 52, 58
  • Mechanism: HPV integrates into the host genome and expresses E6 protein (inactivates p53 tumour suppressor) and E7 protein (inactivates RB tumour suppressor), leading to uncontrolled cell proliferation and suppression of apoptosis
(Robbins & Kumar Basic Pathology)

Q3. Risk Factors

Risk FactorDetails
Early age at first intercourse<16 years significantly increases risk
Multiple sexual partnersIncreases HPV exposure
High-risk male partnerPartner with multiple sexual contacts
High parityMultiple pregnancies
ImmunodeficiencyHIV infection, immunosuppressive therapy
Cigarette smokingCarcinogens in cervical mucus act as co-carcinogens
Long-term use of oral contraceptives>5 years use
Low socioeconomic statusLimited access to screening
Non-barrier contraceptive useIncreases HPV transmission risk
Sexually transmitted infectionsChlamydia, herpes simplex virus 2 as co-factors
(Robbins & Kumar Basic Pathology; Berek & Novak's Gynecology)

Q4. How to Prevent This Condition

Primary Prevention - HPV Vaccination:
  • Bivalent vaccine (Cervarix): Covers HPV 16 & 18
  • Quadrivalent vaccine (Gardasil): Covers HPV 6, 11, 16, 18
  • Nonavalent vaccine (Gardasil 9): Covers HPV 6, 11, 16, 18, 31, 33, 45, 52, 58
  • Recommended for girls aged 9-26 years (ideally before sexual debut)
  • Also recommended for boys to reduce HPV transmission
  • Most effective before HPV exposure
Secondary Prevention - Screening:
  • Pap smear (Papanicolaou test): Detects pre-cancerous lesions (LSIL, HSIL/CIN) before invasive cancer develops; recommended every 3 years from age 21 or within 3 years of first sexual activity
  • HPV co-testing: Combined with Pap smear every 5 years (ages 30-65) for higher sensitivity
  • VIA (Visual Inspection with Acetic Acid) - low-cost screening in resource-limited settings
Other Preventive Measures:
  • Barrier contraception (condoms) - reduces HPV transmission
  • Reducing number of sexual partners
  • Avoiding smoking
  • Treating HIV and other immunocompromising conditions
  • Early treatment of premalignant lesions (CIN) by LEEP, cryotherapy, or cold knife conization


CASE 3

A 25-year-old male, fever for 3 months, weight loss, bilateral cervical matted lymphadenopathy. FNAC: Moderately cellular aspirate - epithelioid cells with slipper-shaped nuclei in small clumps, background lymphocytes, few histiocytes, caseating necrotic debris. ZN stain for AFB - Positive.

Q1. Diagnosis

Tuberculous Lymphadenitis (TB Lymphadenitis / Scrofula)
This is the most common form of peripheral lymphadenopathy due to tuberculosis and the most common form of extrapulmonary TB. The classic FNAC triad is:
  1. Epithelioid cell granulomas - epithelioid histiocytes with "slipper-shaped" (elongated, curved) nuclei, often in clusters
  2. Langhans-type giant cells (may or may not be present)
  3. Caseating necrotic debris in the background
Plus confirmation by ZN stain positivity for AFB = definitive diagnosis.

Q2. Aetiology

  • Primary causative organism: Mycobacterium tuberculosis (human type) - most common
  • Other Mycobacteria:
    • Mycobacterium bovis (bovine type - from unpasteurised milk; less common now)
    • Non-tuberculous mycobacteria (NTM): M. scrofulaceum, M. avium-intracellulare complex (especially in immunocompromised/HIV patients)
Pathogenesis:
  • Primary infection in lungs or oropharynx leads to spread via lymphatics to regional lymph nodes
  • Alternatively, haematogenous spread from a primary focus
  • Macrophages engulf the bacilli but cannot destroy them; this triggers formation of epithelioid granulomas
  • Central caseation necrosis develops due to cell-mediated hypersensitivity (Type IV)
  • Nodes may enlarge, become matted (periadenitis) and eventually soften/liquefy (cold abscess)

Q3. Relevant Investigations

InvestigationDetails
FNAC with ZN stainAlready done - shows AFB (sensitivity ~40-80%)
FNAC culture (Lowenstein-Jensen medium)Gold standard for diagnosis; takes 4-8 weeks; also gives sensitivity
Mantoux test (TST)Intradermal PPD (5TU); induration >10 mm = positive in non-immunocompromised; indicates exposure/infection
Chest X-ray (PA view)Rule out primary pulmonary TB, Ghon complex, hilar lymphadenopathy, miliary TB
Sputum examinationSmear for AFB (ZN stain) + culture + GeneXpert/Xpert MTB/RIF
Complete Blood Count (CBC)Lymphocytosis, elevated ESR, mild anaemia of chronic disease
ESRElevated; non-specific but useful for monitoring
CBNAAT / GeneXpert MTB/RIFRapid molecular test (PCR-based); detects MTB DNA and rifampicin resistance within 2 hours; highly sensitive and specific; can be done on FNAC aspirate
Interferon Gamma Release Assay (IGRA)QuantiFERON-TB Gold / T-SPOT.TB; more specific than Mantoux; detects TB infection
Biopsy of lymph node (excision biopsy)Histopathology if FNAC inconclusive; shows caseating granulomas, Langhans giant cells
HIV testingImportant in young patients with bilateral matted lymphadenopathy and constitutional symptoms
Serum ADA (Adenosine Deaminase)Elevated in TB; useful adjunct
LFT, RFT, visual acuity, audiometryBaseline before starting anti-TB therapy (ATT)
First-line treatment (once diagnosis confirmed): 2HRZE / 4HR - Isoniazid (H), Rifampicin (R), Pyrazinamide (Z), Ethambutol (E) for 2 months intensive phase followed by 4 months continuation phase.

Compiled from Robbins & Kumar Basic Pathology, Berek & Novak's Gynecology, and standard cytopathology references.
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