Scrofuloderma full details for md exams

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Scrofuloderma tuberculosis skin clinical features diagnosis treatment

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Scrofuloderma skin lesion tuberculosis cutaneous

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Here is a comprehensive exam-oriented breakdown of Scrofuloderma for MD examinations:

Scrofuloderma

Definition

Scrofuloderma (also called tuberculosis colliquativa cutis) is a form of cutaneous tuberculosis (TB) caused by direct extension of a tuberculous focus in an underlying structure (lymph node, bone, joint, epididymis) to the overlying skin, resulting in cold abscess formation, ulceration, and sinus tract/fistula development.

Key High-Yield Points at a Glance

FeatureDetail
Causative organismMycobacterium tuberculosis (occasionally M. bovis)
TypeTrue cutaneous TB (reactivation/direct extension)
PathogenesisPer continuitatem spread from underlying focus
Most common underlying focusCervical lymph nodes
Most common siteNeck / submandibular / parotid region
Tuberculin/Mantoux testStrongly positive
Lepromin testNegative
HistologyCaseating granuloma
TreatmentStandard anti-TB regimen (2HRZE + 4HR)

Etiology & Pathogenesis

  • Causative agent: Mycobacterium tuberculosis (acid-fast bacillus)
  • Route: NOT from external inoculation. The bacilli spread per continuitatem (by direct continuity) from an underlying infected focus through the dermis to the skin surface
  • Underlying foci (in order of frequency):
    1. Cervical lymph nodes (most common) — classical "scrofula"
    2. Parotid and submandibular lymph nodes
    3. Infected bones/joints (especially sternoclavicular, sternal)
    4. Epididymis, testis
    5. Lacrimal glands
    6. Salivary glands

Clinical Features

Sites

  • Neck (most common — overlying cervical lymph nodes) — submandibular, parotid, supraclavicular regions
  • Axilla, groin (overlying axillary/inguinal nodes)
  • Chest wall (overlying infected ribs/sternum)

Stages of Lesion Progression

  1. Stage 1 — Subcutaneous nodule: Firm, painless, skin-colored or bluish subcutaneous nodule; overlying skin initially normal
  2. Stage 2 — Softening (fluctuant): Nodule becomes fluctuant (cold abscess) — no warmth, no redness = "cold abscess" (key exam point)
  3. Stage 3 — Ulceration: Skin breaks down → irregular, undermined, ragged, violaceous ulcer with bluish-red overhanging edges
  4. Stage 4 — Sinus/fistula formation: Multiple discharging sinuses and fistulous tracts with thin, seropurulent or caseous discharge
  5. Stage 5 — Healing: Characteristic cord-like, bridge scars (pathognomonic — "bridging scars" or papillomatous scarring)

Exam-Relevant Clinical Points

  • Painless (unless secondary bacterial infection)
  • Cold abscess (no signs of acute inflammation)
  • Undermined/overhanging edges of ulcer
  • Bluish-red to violaceous skin discoloration over the lesion
  • Characteristic bridging/cord scars on healing — pathognomonic
  • Associated systemic TB signs: fever, night sweats, weight loss, malaise
Scrofuloderma showing multiple irregular, deeply ulcerated plaques and nodules on the anterior chest and cervical region with crusted necrotic centers and surrounding post-inflammatory hyperpigmentation and fibrotic scarring
Classic scrofuloderma: ulcerated nodules and plaques in cervical/chest region with fistulous tracts and scarring

Classification of Cutaneous TB (Exam Context)

Scrofuloderma fits into this framework:
TypePathogenesisExample
Primary inoculation TB (chancre)External inoculation, no prior immunityTuberculous chancre
Lupus vulgarisHematogenous/lymphatic spreadMost common cutaneous TB in India
ScrofulodermaDirect extension from underlying focusCold abscess, sinus tracts
Warty TB (TB verrucosa cutis)Exogenous re-inoculation, high immunityVerrucous plaques on hands/feet
Miliary TBHematogenous spread (severe immunosuppression)Disseminated papules
TuberculidsHypersensitivity reaction (not direct infection)Erythema induratum, PNT

Diagnosis

1. Mantoux (Tuberculin Skin Test / PPD)

  • Strongly positive (>10 mm in immunocompetent; >5 mm in immunocompromised)
  • High-grade immunity in scrofuloderma

2. Histopathology (Biopsy — Gold Standard for Morphology)

  • Caseating epithelioid granulomas in the dermis
  • Langhans giant cells surrounded by epithelioid histiocytes
  • Central caseous necrosis
  • Peripheral lymphocytic infiltrate

3. Microbiological Investigations

  • Ziehl-Neelsen (ZN) stain: AFB (acid-fast bacilli) may be seen in discharge/biopsy — key exam point
  • Culture on Lowenstein-Jensen (LJ) medium: Gold standard for confirmation; slow (6–8 weeks)
  • CBNAAT/GeneXpert (Nucleic Acid Amplification Test): Rapid molecular diagnosis; also detects rifampicin resistance

4. IGRA (Interferon-Gamma Release Assay)

  • QuantiFERON-TB Gold or T-SPOT.TB
  • Positive; more specific than Mantoux (no false positives with BCG)

5. Imaging

  • Chest X-ray: Look for pulmonary TB (primary focus)
  • Ultrasound neck: Assess underlying lymph node involvement, matting, cold abscess
  • CT scan: Defines extent of deep tissue involvement

Differential Diagnosis

ConditionDifferentiating Feature
ActinomycosisSulphur granules in discharge; jaw/neck; Gram+ filamentous organisms
BotryomycosisBacterial; Gram stain shows cocci/rods
SporotrichosisLymphocutaneous pattern; fungal (Sporothrix schenckii)
Syphilitic gummaTertiary syphilis; VDRL/TPHA positive; non-caseating gumma
Hidradenitis suppurativaAxilla/groin; recurrent abscesses; no TB
Atypical mycobacterial infectionCulture differentiates (M. avium, M. scrofulaceum)
Lymphoma with cutaneous involvementBiopsy; lymph node histology

Treatment

Anti-TB Regimen (Standard WHO/RNTCP/NTEP)

2HRZE / 4HR
PhaseDurationDrugs
Intensive phase2 monthsIsoniazid (H) + Rifampicin (R) + Pyrazinamide (Z) + Ethambutol (E)
Continuation phase4 monthsIsoniazid (H) + Rifampicin (R)
  • Total duration: 6 months for cutaneous TB (most forms)
  • Some guidelines recommend 9 months if bone/joint involvement coexists
  • Daily regimen preferred over intermittent (NTEP, India)

Adjunctive Measures

  • Treat underlying focus (lymph node drainage if very large and tense; surgical excision rarely needed)
  • Incision and drainage alone is contraindicated — risk of chronic sinus formation and spread
  • Nutritional support, address HIV/immunosuppression

Monitoring

  • Clinical response (healing of ulcers, closure of sinuses) expected within 2–3 months
  • Liver function tests (HRZE are all hepatotoxic — especially INH, RIF, PZA)
  • Ophthalmic review if on Ethambutol (ethambutol optic neuropathy)

Prognosis & Complications

  • Good prognosis with complete anti-TB therapy
  • Residual scarring is universal — characteristic cord/bridge scars
  • Complications:
    • Secondary bacterial infection
    • Lymphedema from lymph node destruction
    • Contractures due to extensive fibrosis
    • Marjolin's ulcer (squamous cell carcinoma arising in chronic scrofuloderma scar — rare but important exam point)

High-Yield Mnemonics & Exam Traps

PointDetails
"Scrofula" = cervical TB lymphadenitisScrofuloderma = when scrofula breaks through skin
Cold abscessNo heat/redness — classic for TB abscess
Bridging scars = pathognomonicAsk in MCQs
ZN stain positiveUnlike lupus vulgaris (AFB rarely seen) — scrofuloderma has more bacilli
Do NOT I&DIncision alone worsens disease
Marjolin's ulcer riskIn long-standing unhealed scrofuloderma
Most common cutaneous TB in IndiaLupus vulgaris (not scrofuloderma)
Scrofuloderma vs. Lupus vulgarisLV = hematogenous spread + apple jelly nodules on diascopy; Scrofuloderma = direct extension + cold abscess

Summary Box (Quick Recall)

Scrofuloderma = Cutaneous TB caused by direct extension (per continuitatem) from underlying TB focus (most commonly cervical lymph nodes) → cold abscess → ulcer with undermined edgesdischarging sinuses → heals with bridging cord scars (pathognomonic). Diagnosed by caseating granuloma on histology + AFB on ZN stain. Treated with 2HRZE/4HR.
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