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Cutaneous Tuberculosis (Cutaneous TB) — Complete MD Exam Notes


1. Introduction

Cutaneous tuberculosis (CTB) refers to skin lesions caused by Mycobacterium tuberculosis, M. bovis, or the BCG bacillus. It accounts for ~1–2% of all TB cases and ~2% of all dermatological conditions in endemic regions. The skin may be infected via exogenous inoculation, endogenous spread (hematogenous, lymphatic, contiguous), or hypersensitivity reactions (tuberculids).

2. Pathogen

  • Mycobacterium tuberculosis — aerobic, acid-fast bacillus (AFB)
  • M. bovis — from infected animals/unpasteurized milk
  • BCG strain — following BCG vaccination (rare, mostly in immunocompromised)

3. Pathogenesis / Routes of Infection

RouteType
Exogenous inoculationPrimary inoculation TB, Tuberculosis verrucosa cutis
Endogenous — hematogenousLupus vulgaris, Acute miliary TB, Metastatic tuberculous abscess
Endogenous — direct/lymphatic extensionScrofuloderma, Orificial TB
Immunological reaction (tuberculids)Lichen scrofulosorum, Papulonecrotic tuberculid, Erythema induratum of Bazin

4. Classification

A. TRUE CUTANEOUS TB (Organisms Present in Skin)

1. Primary Inoculation Tuberculosis (Tuberculous Chancre)

  • Occurs in: Previously uninfected individuals (primary infection)
  • Route: Direct inoculation (cuts, abrasions — laboratory workers, pathologists, medical personnel)
  • Features:
    • Chancre: Painless, indurated papule → ulcer at inoculation site (face, hands, feet)
    • After 3–8 weeks: Regional lymphadenopathy ("Primary complex" = chancre + lymphadenopathy)
    • Heals spontaneously in most, may disseminate
  • Histology: Initially non-specific inflammation → later caseating granulomas
  • AFB: Sometimes positive in lesion, usually positive in nodes

2. Tuberculosis Verrucosa Cutis (Warty TB)

  • Occurs in: Previously sensitized individuals (re-infection)
  • Route: Exogenous inoculation
  • At risk: Pathologists, butchers, laboratory workers, children (playing barefoot in endemic areas)
  • Features:
    • Begins as small, painless, hyperkeratotic papule
    • Evolves into verrucous (warty), irregular plaque with a "pebbly" or papillomatous surface
    • Site: dorsum of hands, fingers, feet, ankles
    • No lymphadenopathy (sensitized host)
    • Indolent; may persist for years
  • Old names: Prosector's wart, Butcher's wart, Anatomist's wart
  • Histology: Pseudoepitheliomatous hyperplasia, caseating granulomas in dermis, AFB rare
  • Mantoux: Strongly positive

3. Lupus Vulgaris

  • Most common form of CTB in India
  • Occurs in: Previously sensitized, high-immunity individuals
  • Route: Hematogenous spread; also direct extension from lymph nodes/bones; or post-primary inoculation
  • Features:
    • Most commonly on head and neck (nose, cheek — "butterfly" distribution), also extremities
    • Begins as soft, reddish-brown papules → coalesce into plaques
    • Pathognomonic sign — Apple-jelly (Lupoid) nodules: Yellowish-brown translucent nodules visible on diascopy (pressing glass slide on skin)
    • Central scarring with active spreading periphery
    • Active edge + healing periphery can coexist (see image below)
    • Slow, relentlessly progressive — can persist for decades
    • Complications: Destruction of nasal cartilage, ectropion; squamous cell carcinoma can develop in scars (Marjolin's ulcer)
  • Histology: Non-caseating or minimally caseating tuberculoid granulomas; Langerhans giant cells; AFB very rare
  • Mantoux: Strongly positive
According to Harrison's Principles of Internal Medicine, 21st Ed. (p. 1605): "Lesions occur primarily in the head and neck region and are red-brown plaques with a yellow-brown color on diascopy. Secondary scarring can develop within the central portion of the plaques. Cultures or PCR analysis of the lesions should be performed, along with an interferon γ release assay of peripheral blood, because it is rare for the acid-fast stain to show bacilli within the dermal granulomas."
Clinical photograph — Lupus Vulgaris:
Lupus Vulgaris
Large variegated plaque showing active erythematous border (double arrows) and healing/scarring periphery (single arrow) — characteristic of lupus vulgaris

4. Scrofuloderma

  • Occurs in: Children and young adults
  • Route: Contiguous spread from underlying infected lymph node (cervical most common), bone, or joint
  • Features:
    • Initially: Firm, painless, non-tender subcutaneous nodule overlying infected node (usually cervical, axillary, or inguinal)
    • Nodule softens → skin becomes bluish-red, adherent, fluctuant
    • Breaks down to form irregular ulcers with undermined, "collar-stud" edges, and sinuses discharging watery pus/caseous material
    • Heals with cord-like, bridge scars (pathognomonic)
  • Histology: Caseating necrosis, granulomas; AFB often found
  • Mantoux: Usually positive
  • DDx: Actinomycosis, atypical mycobacteriosis, syphilitic gumma, hidradenitis suppurativa

5. Orificial Tuberculosis (Tuberculosis Cutis Orificialis)

  • Rarest and most severe form
  • Occurs in: Severely immunocompromised with advanced internal TB
  • Route: Autoinoculation — organisms from internal lesions (pulmonary, GI, genitourinary TB) shed into body orifices
  • Features:
    • Sites: Around oral cavity (tongue, soft palate — from pulmonary TB), perianal region (from GI/GU TB), genitalia
    • Painful, punched-out ulcers with undermined edges, yellowish base; may have "soft palate perforations"
    • Poor prognosis; indicates terminal disease
  • Histology: Caseating granulomas; AFB readily found
  • Mantoux: May be negative (anergy due to severe immunosuppression)

6. Acute Miliary Tuberculosis Cutis

  • Occurs in: Severely immunocompromised (infants, HIV, post-measles)
  • Route: Hematogenous dissemination from primary focus
  • Features: Multiple tiny papules, vesicles, or pustules — widespread over trunk; poor prognosis
  • Histology: Non-specific initially; AFB may be found; granulomas form later

7. Metastatic Tuberculous Abscess (Tuberculous Gumma)

  • Occurs in: Immunocompromised (poor host immunity)
  • Route: Hematogenous spread from primary focus (often during latent TB reactivation)
  • Features:
    • Cold, painless, fluctuant subcutaneous abscess without signs of acute inflammation
    • "Cold abscess" — may be single or multiple
    • Spontaneously ruptures → sinus formation
  • Sites: Trunk, extremities
  • AFB: Usually found in aspirate

B. TUBERCULIDS (Immunological / Hypersensitivity Reactions)

Tuberculids are hypersensitivity reactions to M. tuberculosis antigens in a host with high immunity but no organisms in the skin. AFB are absent (or very rarely found by PCR). They resolve with anti-TB treatment.

1. Lichen Scrofulosorum

  • Most common tuberculid
  • Age: Children and adolescents
  • Features:
    • Asymptomatic, lichenoid, minute (1–3 mm) perifollicular or periductal papules
    • Grouped in discoid or annular plaques
    • Sites: Trunk (especially chest, abdomen)
    • Spontaneously resolves
  • Histology: Superficial perifollicular/periductal granulomas; no caseation; no AFB
  • Mantoux: Strongly positive
  • Association: Usually with underlying lymph node or bone TB

2. Papulonecrotic Tuberculid

  • Features:
    • Recurrent, symmetrical, necrotic papules and pustules
    • Heal with depressed, "punched-out" scars
    • Sites: Extensor surfaces of extremities (elbows, knees, buttocks)
  • Histology: Obliterative vasculitis, wedge-shaped necrosis; no AFB
  • Mantoux: Positive
  • DDx: Pityriasis lichenoides, leukocytoclastic vasculitis

3. Erythema Induratum of Bazin

  • Features:
    • Recurrent, tender, indurated erythematous nodules and plaques
    • Ulcerate and leave atrophic scars
    • Sites: Posterior calves (calves of legs — "stockings area")
    • Predominantly in middle-aged women
    • Associated with cold weather (cold panniculitis)
  • Pathology: Lobular panniculitis with vasculitis and granulomas
  • Note: When no TB link found → called "Nodular vasculitis"
  • Mantoux: Positive; MTB-PCR may be positive in lesion

4. Rosai-Dorfman Disease (associated in some classifications)

(Less commonly listed but some classify here)

5. Summary Comparison Table

FeaturePrimary Inoculation TBTB Verrucosa CutisLupus VulgarisScrofulodermaOrificial TBTuberculids
ImmunityNone (primary)Sensitized (high)Sensitized (high)VariableLowVery high
AFB in skin+/-RareVery rareOften +Readily +Absent
RouteExogenousExogenousHematogenousContiguousAutoinoculationHypersensitivity
Mantoux+ (late)+++++-/++++
Key featureChancre + LAPWarty plaqueApple-jelly nodulesCold abscess + bridge scarsPainful ulcers at orificesSterile; respond to ATT

6. Diagnosis

A. Clinical

  • Site, morphology, epidemiology, contact history, BCG scar

B. Mantoux (Tuberculin Skin Test)

  • Positive in most forms (strongly positive in tuberculids, lupus vulgaris, TB verrucosa)
  • Negative (anergy) in orificial TB and miliary TB (immunocompromised)

C. Laboratory

TestDetails
AFB smearLow sensitivity in CTB (bacilli sparse)
Culture (Lowenstein-Jensen medium)Gold standard — 6–8 weeks; low yield in paucibacillary forms
HistopathologyCaseating/non-caseating epithelioid granulomas with Langerhans giant cells (Bailey & Love, 28th Ed., p. 619)
PCR (IS6110 gene)Rapid, sensitive; best for paucibacillary forms (lupus vulgaris, tuberculids)
IGRA (Interferon-γ Release Assay)QuantiFERON-TB Gold / T-SPOT; confirms sensitization; unaffected by BCG
CBC, ESRNon-specific; elevated ESR
Chest X-rayDetect underlying pulmonary TB
Harrison's (p. 1605): "Cultures or PCR analysis of the lesions should be performed, along with an interferon γ release assay of peripheral blood."

D. Histopathology (Key for Exam)

  • Caseating granuloma: Epithelioid cells + Langerhans giant cells + lymphocytes surrounding central caseous necrosis
  • Non-caseating granuloma: Seen in lupus vulgaris, tuberculids (high immunity)
  • "Apple-jelly" correlate: Tuberculoid granulomas in upper dermis

7. Differential Diagnosis

CTB TypeKey DDx
Lupus vulgarisSarcoidosis, lupus erythematosus, leishmaniasis, leprosy
TB verrucosa cutisVerruca vulgaris, chromoblastomycosis, blastomycosis
ScrofulodermaActinomycosis, syphilitic gumma, hidradenitis suppurativa
Erythema induratumNodular vasculitis, erythema nodosum, polyarteritis nodosa
Orificial TBAphthous ulcers, Crohn's disease, SCC

8. Treatment

Anti-Tubercular Therapy (ATT)

Standard regimen (same as pulmonary TB):
PhaseDurationDrugs
Intensive phase2 monthsIsoniazid (H) + Rifampicin (R) + Pyrazinamide (Z) + Ethambutol (E) → 2HRZE
Continuation phase4 monthsIsoniazid (H) + Rifampicin (R) → 4HR
Total6 months
  • In lupus vulgaris and severe/extensive disease: may extend continuation phase to 7 months (total 9 months)
  • Tuberculids: Usually respond to 6-month regimen

Adjunctive / Surgical

  • Surgical excision for localized TB verrucosa cutis (small lesions)
  • Drainage for cold abscesses (scrofuloderma, tuberculous gumma)
  • Reconstructive surgery for disfiguring scars (post-treatment)

Monitoring

  • Clinical response in 4–8 weeks
  • LFTs at baseline and monthly (rifampicin/INH hepatotoxicity)
  • Visual acuity/color vision (ethambutol — optic neuritis)

9. Complications

ComplicationForm
Squamous cell carcinomaLupus vulgaris (Marjolin's ulcer)
Destruction of nasal cartilage, ectropionLupus vulgaris
Disfiguring bridge-like scarsScrofuloderma
Drug resistanceMDR-TB (if irregular treatment)

10. High-Yield Points for MD Exam

  1. Most common CTB in India = Lupus vulgaris
  2. Pathognomonic sign of LV = Apple-jelly nodules on diascopy
  3. Warty TB = TB verrucosa cutis (prosector's wart — occurs in sensitized)
  4. Bridge-like/cord scars = Scrofuloderma
  5. Mantoux negative in CTB = Orificial TB (anergy), Miliary TB
  6. No organisms in skin = Tuberculids
  7. Most severe form = Orificial TB (terminal disease)
  8. Cold abscess = Scrofuloderma or Tuberculous gumma
  9. Posterior calf ulcerating nodules in women = Erythema induratum of Bazin
  10. PCR target gene = IS6110 of M. tuberculosis
  11. Gold standard culture medium = Lowenstein-Jensen (L-J) medium
  12. Complication of LV = SCC in scar
  13. Treatment = 2HRZE + 4HR (6 months total)
  14. IGRA not affected by BCG vaccination (unlike Mantoux)

Sources: Harrison's Principles of Internal Medicine, 21st Ed. (p. 1605); Bailey & Love's Short Practice of Surgery, 28th Ed. (p. 619); supplemented from standard dermatology references (Rook's Textbook of Dermatology, IADVL Textbook of Dermatology)
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