What are the diagnostic steps for cutaneous tuberculosis in a patient with skin lesions?

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Diagnostic Testing for Cutaneous Tuberculosis

For suspected cutaneous tuberculosis, obtain a skin biopsy for both histopathology and mycobacterial culture, perform tuberculin skin testing (TST) or interferon-gamma release assay (IGRA), and obtain a chest radiograph to evaluate for pulmonary involvement. 1, 2

Initial Clinical Assessment

When evaluating skin lesions suspicious for cutaneous TB, look for these specific features:

  • Lesion morphology patterns: Verrucous plaques, ulcerations, nodules, abscesses, or lupus vulgaris-type lesions 1, 3
  • Constitutional symptoms: Persistent cough >3 weeks, night sweats, weight loss, anorexia, or fever 4
  • Exposure history: Contact with active TB cases, travel to endemic areas, or residence in high-prevalence regions 4
  • HIV status: Must be determined as it affects diagnostic interpretation and treatment approach 4

Diagnostic Algorithm

Step 1: Skin Biopsy (Essential)

Obtain a skin biopsy and submit for BOTH culture and histopathology simultaneously 1, 2

  • Culture: Request mycobacterial culture specifically, as M. tuberculosis has a low bacillary load in cutaneous lesions 2, 5
  • Histopathology: Look for granulomatous inflammation, though some cases show only nonspecific inflammation without classic granuloma formation 1
  • Acid-fast bacilli (AFB) staining: Perform on tissue, though sensitivity is limited in paucibacillary forms 2, 5

Critical caveat: Multibacillary forms (tuberculous chancre, scrofuloderma, orificial TB) are easier to diagnose bacteriologically, while paucibacillary forms (lupus vulgaris, tuberculosis verrucosa cutis) require correlation of clinical, epidemiological, and histological data 5

Step 2: Tuberculin Skin Testing

Administer PPD using the Mantoux technique: 0.1 mL of PPD (5 tuberculin units) intracutaneously on the volar or dorsal forearm 4, 6

  • Proper injection: Should produce a 6-10 mm wheal 4, 6
  • Reading timing: Must be read by trained personnel at 48-72 hours, measuring only induration (not erythema) in millimeters 4, 6

Interpretation cutoffs:

  • ≥5 mm positive: HIV-infected patients, recent TB contacts, immunosuppressed patients (≥15 mg prednisone daily for ≥1 month), organ transplant recipients, or those with fibrotic chest radiograph changes 6, 7
  • ≥10 mm positive: Moderate-risk individuals 6
  • ≥15 mm positive: Low-risk individuals with no known risk factors 6

Important limitation: A negative TST does NOT rule out cutaneous TB, as false-negative rates reach 25% in active TB and are higher in HIV-infected patients 4, 7

Step 3: Chest Radiography

Obtain a chest radiograph in ALL suspected cutaneous TB cases 4, 7

  • Approximately one-third of cutaneous TB cases have concurrent systemic involvement 3
  • Look for apical cavitary disease, infiltrates in any lung zone, or mediastinal/hilar adenopathy 4
  • HIV-infected patients may have atypical radiographic presentations or even normal chest radiographs despite active disease 4

Step 4: Molecular Testing (When Initial Tests Are Inconclusive)

If histopathology is nonspecific and cultures are negative or pending, utilize PCR amplification 1, 2

  • PCR has proven invaluable for identifying M. tuberculosis from skin biopsies when cultures are negative 1
  • Offers rapid results with high sensitivity and specificity 2
  • Particularly useful in paucibacillary forms where AFB stains and cultures are typically negative 5

Alternative: Consider IGRA testing (QuantiFERON-TB Gold or T-SPOT.TB) as an adjunct or alternative to TST, especially if patient cannot return for TST reading 6

Step 5: Additional Bacteriologic Studies

If pulmonary symptoms are present or chest radiograph is abnormal, collect sputum specimens 4, 7

  • Obtain 3-5 sputum specimens on different days for AFB smear and mycobacterial culture 4
  • Negative sputum smears do not exclude pulmonary TB 4

Common Diagnostic Pitfalls

  • Do not dismiss positive TST in BCG-vaccinated patients: Interpret positive reactions as M. tuberculosis infection when the patient is at increased risk 7
  • Do not rely on anergy testing: The CDC explicitly recommends against anergy testing in HIV-infected or immunocompromised patients due to lack of standardization and poor reproducibility 4, 7
  • Do not accept patient self-reading of TST: Only trained personnel should read and interpret results 4, 6
  • Do not measure erythema: Only induration should be measured and recorded 4, 6, 7
  • Do not delay biopsy: Cutaneous TB diagnosis is challenging and requires tissue confirmation, as clinical mimicry of other conditions is common 3
  • Do not assume isolated cutaneous disease: Always evaluate for systemic involvement with chest radiograph and symptom assessment 3

Classification Context

Once diagnosis is established, patients should be classified according to the American Thoracic Society/CDC framework as Class 3 (clinically active tuberculosis) if they have clinical, bacteriological, and/or radiographic evidence of current disease 4

References

Research

Cutaneous Tuberculosis.

Microbiology spectrum, 2017

Research

Cutaneous tuberculosis: diagnosis and treatment.

American journal of clinical dermatology, 2002

Research

Cutaneous tuberculosis. Part I: Pathogenesis, classification, and clinical features.

Journal of the American Academy of Dermatology, 2023

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

[Clinical forms of the cutaneous tuberculosis].

Bulletin de la Societe de pathologie exotique (1990), 2003

Guideline

PPD Screening for Tuberculosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

TB Skin Test Interpretation in HIV/AIDS and Immunocompromised Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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