Pulmonology focuses on diagnosing and treating lung and airway conditions such as asthma, COPD, and pneumonia, as well as overall respiratory health.

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The Diagnostic Puzzle

Diagnosing tuberculosis is a complex process that requires integrating clinical clues, immunological evidence, radiographic patterns, and microbiological data. Because latent tuberculosis infection is asymptomatic and active disease can be subtle or atypical, Liv Hospital utilizes a comprehensive diagnostic algorithm. The goal is two-fold: to identify those with latent infection who would benefit from preventive therapy, and to diagnose active disease to initiate treatment and rapidly stop transmission.

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Immunological Testing: Determining Infection Status

These tests tell us if the immune system has “seen” the TB bacteria, but they cannot distinguish between latent infection and active disease.

The Tuberculin Skin Test (TST) / Mantoux

This is the traditional screening method, in use for over a century.

  • Technique: A standardized dose of PPD (Purified Protein Derivative) is injected intradermally (between skin layers) on the forearm.
  • Reading: The test must be read by a trained professional within 48-72 hours. The measurement is based on the induration (palpable hardness), not the redness (erythema).
  • Interpretation Criteria: The threshold for a tuberculosis mantoux test positive result varies by risk:
    • >5 mm: Positive for HIV+ persons, recent contacts of active cases, or those with fibrotic chest X-rays.
    • >10 mm: Positive for recent immigrants from high-prevalence countries, IV drug users, residents of high-risk settings, children <4 years, and those with medical risk factors (diabetes, kidney failure).
    • >15 mm: Positive for persons with no known risk factors.
  • The Booster Phenomenon: In older adults, the first test may be negative due to waned immunity. A second test, 1-3 weeks later, may elicit a positive reaction (a boost), indicating an old infection rather than a new conversion. This is the basis for “two-step testing.”

Interferon-Gamma Release Assays (IGRAs)

Modern blood tests like QuantiFERON-TB Gold Plus and T-SPOT.TB.

  • Mechanism: They measure the release of interferon-gamma by T-cells in response to specific M. tuberculosis antigens (ESAT-6, CFP-10).
  • Advantages:
    • Specificity: These antigens are not found in the BCG vaccine strain, so IGRAs do not produce false positives in vaccinated individuals—a huge advantage in many countries.
    • Logistics: Single patient visit; no need to return for reading.
    • Objectivity: No reader bias compared to measuring skin induration.
  • Role: They are the preferred test for BCG-vaccinated individuals and those who may not return for TST reading.
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Radiological Imaging: Visualizing the Damage

Chest Radiography

The chest x-ray is the cornerstone of evaluation for pulmonary TB.

  • Primary TB: Often seen in children. Typically shows lower lobe infiltrates and hilar/mediastinal lymphadenopathy (enlarged lymph nodes).
  • Reactivation TB: The classic adult presentation. Typically involves the apical and posterior segments of the upper lobes (where oxygen tension is highest).
    • Cavitation: The hallmark of advanced, highly infectious disease. Thick-walled cavities may show air-fluid levels.
    • Fibrosis: Scarring and volume loss in the upper lobes.
  • Miliary TB: A distinct pattern of diffuse, uniform, millet-seed-sized nodules (1-2mm) distributed throughout both lung fields.
  • HIV/TB Coinfection: The pattern changes as immunity declines. In advanced HIV, X-rays may look like primary TB (lower lobe, adenopathy) or may even be normal.

Computed Tomography (CT)

CT scans are far more sensitive than X-rays.

  • Early Detection: Can detect subtle “tree-in-bud” opacities (indicating endobronchial spread) or small cavities invisible on X-ray.
  • Extrapulmonary: Essential for evaluating bone destruction (spine CT/MRI), abdominal involvement, or brain lesions.

Microbiological Confirmation: The Gold Standard

While other tests suggest TB, identifying the organism is proof.

Sputum Collection

Three separate sputum specimens are collected, ideally 8-24 hours apart, with at least one early morning sample (when bacterial load is highest). Induced sputum (using nebulized saline) or bronchoscopy may be needed if the patient cannot cough.

Smear Microscopy

  • AFB Smear: Staining the sputum (Ziehl-Neelsen or fluorochrome stain) to look for Acid-Fast Bacilli.
  • Pros: Rapid (results in 24 hours), identifies the most infectious patients.
  • Cons: Low sensitivity (requires >5,000 bacilli/mL), cannot distinguish viable from dead bacteria, cannot distinguish TB from non-tuberculous mycobacteria (NTM).

Nucleic Acid Amplification Tests (NAAT) / PCR

Tests like the Xpert MTB/RIF Ultra have revolutionized diagnosis.

  • Mechanism: Amplifies DNA sequences specific to the M. tuberculosis complex.
  • Pros: Highly sensitive and specific. Provides results in <2 hours. Crucially, it can also detect mutations conferring Rifampin resistance, acting as an early warning for MDR-TB.
  • Role: Recommended by WHO as the initial diagnostic test for all persons with signs of TB.

Bacterial Culture

Still the definitive “gold standard.”

  • Solid Media (Lowenstein-Jensen): Traditional, takes 4-8 weeks for growth.
  • Liquid Media (MGIT): Faster, takes 1-3 weeks.
  • Importance: Culture is the only method for comprehensive Drug Susceptibility Testing (DST) of all first- and second-line drugs, which is essential for designing effective treatment regimens. It also confirms the bacteria are alive.

Diagnosis of Extrapulmonary TB

Requires obtaining tissue or fluid from the affected site.

  • Biopsy: Fine needle aspiration (FNA) of lymph nodes or surgical biopsy of pleura/bone. Histology shows “caseating granulomas.”
  • Fluid Analysis: Pleural fluid, CSF, or ascites fluid usually shows high protein, low glucose, and a predominance of lymphocytes. ADA (Adenosine Deaminase) levels in these fluids are a valuable marker for TB.

Diagnostic Algorithms in Special Populations

  • Children: Often swallow sputum. Gastric aspirates (suctioning stomach fluid in the morning) are used for culture. Diagnosis often relies on the “triad” of a positive skin test, an abnormal X-ray, and a history of exposure.

HIV: Diagnosis is more complex due to atypical presentation and lower bacterial loads (paucibacillary disease). Urine LAM (lipoarabinomannan) antigen testing is a functional bedside test for advanced HIV patients.

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Assoc. Prof. MD. Engin Aynacı Assoc. Prof. MD. Engin Aynacı Pulmonology Overview and Definition
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FREQUENTLY ASKED QUESTIONS

Can I have a false positive skin test?

Yes, if you received the BCG vaccine (common in Europe/Asia/Africa) or were exposed to non-tuberculosis mycobacteria (environmental bacteria), the skin test can be falsely positive; a blood test (IGRA) avoids this.

This specific CT scan pattern resembling a budding tree branch indicates that infection is spreading through the small airways (bronchioles) and is highly suggestive of active TB.

Because TB bacteria grow very slowly, a final culture result can take 2 to 8 weeks, although liquid cultures usually turn positive within 10 to 14 days.

Yes, the Xpert MTB/RIF test is highly accurate, detecting TB in about 98% of smear-positive cases and about 70% of smear-negative instances, and it also detects drug resistance.

Since bacteria are not released continuously, taking three samples (especially morning samples) significantly increases the chance of finding them if they are present.

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