Pneumology - Original Articles
4 September 2025

Diagnostic utility of flexible bronchoscopy in smear-negative and atypical lung infections: identifying tuberculosis, fungal, and non-tuberculous mycobacteria infections and malignancy

Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
29
Views
9
Downloads

Authors

Fiber-optic bronchoscopy (FOB) plays a crucial role in the diagnosis and management of various pulmonary diseases by offering direct visualization of the airways and enabling targeted sampling for microbiological and histopathological evaluation. This study aimed to assess the clinical, radiological, microbiological, and histopathological profiles of patients undergoing FOB. A retrospective analysis of 103 participants who underwent the procedure over one year was conducted. After obtaining informed consent, demographic and clinical information was recorded, and relevant radiological findings were noted. The procedure was performed under local anesthesia. In all cases with inconclusive sputum evaluation, bronchoalveolar lavage (BAL) was conducted, with additional brushing and biopsy performed in selected participants. The collected samples were analyzed to determine the underlying etiology. Among the 103 individuals studied, 52.4% were female, with a mean age of 54.82 years, and the majority (82.5%) were over 40 years old. Cough was the most common symptom (73.78%), followed by breathlessness. The frequent comorbidities included diabetes (27.18%) and hypertension (18.4%). Radiological patterns commonly included consolidation (59%) and cavitary lesions (30.1%). On bronchoscopy, secretions (67%) and inflamed mucosa (26%) were the most frequent findings. BAL cultures were positive in 48% of cases, with Klebsiella being the predominant organism. Tuberculosis was confirmed in 32% of the cases. Histopathology confirmed malignancy in 5.8%, mainly adenocarcinoma. In 24.2% of participants, the procedure was inconclusive. Overall, FOB was found to be a safe and valuable tool in diagnosing a spectrum of pulmonary conditions, especially in smear-negative tuberculosis, fungal and atypical infections, and malignancies, aiding targeted therapy and better clinical outcomes.

Altmetrics

Downloads

Download data is not yet available.

Citations

Mullerova H, Shukla A, Hawkins A, et al. Risk factors for acute exacerbations of COPD in a primary care population: a retrospective observational cohort study. BMJ Open 2014;4:e006171. DOI: https://doi.org/10.1136/bmjopen-2014-006171
Merino-Sanchez M, Alfageme-Michavila I, Reyes Nuñez N, et al. Prognosis in patients with pneumonia and chronic obstructive pulmonary disease. Arch Bronconeumol 2005;41:607-11. [Article in Spanish]. DOI: https://doi.org/10.1016/S1579-2129(06)60294-2
Prakash UB, Offord KP, Stubbs SE. Bronchoscopy in North America: the ACCP survey. Chest 1991;100:1668-75. DOI: https://doi.org/10.1378/chest.100.6.1668
Prabhakar, K, Gattu, R Reddy, et al. Diagnostic role of fiberoptic bronchoscopy in various respiratory diseases at esic medical college hospital Sanath Nagar. Int J Health Sci 2022;6:3125-31. DOI: https://doi.org/10.53730/ijhs.v6nS9.13223
Alamoudi OS, Attar SM, Ghabrah TM, et al. Bronchoscopy, indications, safety and complications. Saudi Med J 2000;21:1043-7.
Alzeer AH, Al-Otair HA, Al-Hajjaj MS. Yield and complications of flexible fiberoptic bronchoscopy in a teaching hospital. Saudi Med J 2008;29:55-9.
Sawy MS, Jayakrishnan B, Behbehani N, et al. Flexible fiberoptic bronchoscopy. Diagnostic yield. Saudi Med J 2004;25:1459-63.
Taha AS. Flexible fibreoptic bronchoscopy in Basra, Iraq: a 20-month experience. East Mediterr Health J 2000;6:226-32. DOI: https://doi.org/10.26719/2000.6.2-3.226
Qanash S, Hakami OA, Al-Husayni F, et al. Flexible fiberoptic bronchoscopy: indications, diagnostic yield and complications. Cureus 2020;12:e11122. DOI: https://doi.org/10.7759/cureus.11122
Iyer VN, Joshi AY, Boyce TG, et al. Bronchoscopy in suspected pulmonary TB with negative induced-sputum smear and MTD((R)) Gen-probe testing. Resp Med 2011;105:1084-90. DOI: https://doi.org/10.1016/j.rmed.2011.03.003
Singhal S, Gaidhane AM, Khatib N, et al. Use of flexible bronchoscopy for rapid diagnosis of suspected tubercular cases in rural India. J Infect Dev Ctries 2009;3:860-4. DOI: https://doi.org/10.3855/jidc.608
Thorat J, Malhotra P, Bhanshe P, et al. Clinical utility of stepwise bronchoalveolar lavage fluid analysis in diagnosing and managing lung infiltrates in leukemia/lymphoma patients with febrile neutropenia. JCO Glob Oncol 2024;10:e2300292. DOI: https://doi.org/10.1200/GO.23.00292
Yamasaki K, Kawanami T, Yatera K, et al. Significance of anaerobes and oral bacteria in community-acquired pneumonia. PLoS One 2013;8:e63103. DOI: https://doi.org/10.1371/journal.pone.0063103
Jacomelli M, Silva PR, Rodrigues AJ, et al. Bronchoscopy for the diagnosis of pulmonary tuberculosis in patients with negative sputum smear microscopy results. J Bras Pneumol 2012;38:167-73. DOI: https://doi.org/10.1590/S1806-37132012000200004
Oh JY, Lee SS, Kim HW, et al. Additional usefulness of bronchoscopy in patients with initial microbiologically negative pulmonary tuberculosis: a retrospective analysis of a Korean nationwide prospective cohort study. Infect Drug Resist 2022;15:1029-37. DOI: https://doi.org/10.2147/IDR.S354962
Vélez L, Correa LT, Maya MA, et al. Diagnostic accuracy of bronchoalveolar lavage samples in immunosuppressed patients with suspected pneumonia: analysis of a protocol. Respir Med 2007;101:2160-7. DOI: https://doi.org/10.1016/j.rmed.2007.05.017
Kottmann RM, Kelly J, Lyda E, et al. Bronchoscopy with bronchoalveolar lavage: determinants of yield and impact on management in immunosuppressed patients. Thorax 2011;66:823. DOI: https://doi.org/10.1136/thx.2010.145540
Vivek KU, Nutan Kumar DM. Microbiological profile of bronchoalveolar lavage fluid in patients with chronic respiratory diseases: a tertiary care hospital study. Int J Med Res Rev 2016;4:330-7. DOI: https://doi.org/10.17511/ijmrr.2016.i03.08
Lin SH, Kuo PH, Hsueh PR, et al. Sputum bacteriology in hospitalized patients with acute exacerbation of chronic obstructive pulmonary diseasein Taiwan with an emphasis on Klebsiella pneumonia and Pseudomonas aeruginosa. Respirology 2007;12:81-7. DOI: https://doi.org/10.1111/j.1440-1843.2006.00999.x
Singh AK, Sen MR, Anupurba S, et al. Antibiotic sensitivity pattern of the bacteria isolated from nosocomial infections in ICU. J Commun Dis 2002;34:257-63.
Han SJ, Chung C, Park D. Complete resolution of non-tuberculous mycobacterial pulmonary nodule following cryobiopsy: the first case report. Diagn Pathol 2025;20:42. DOI: https://doi.org/10.1186/s13000-025-01644-z
Bethencourt Mirabal A, Nguyen AD, Ferrer G. Lung nontuberculous mycobacterial infections. Treasure Island, FL, USA: StatPearls Publishing; 2025.
Urabe N, Sakamoto S, Ito A, et al. Bronchial brushing and diagnosis of pulmonary nontuberculous mycobacteria infection. Respiration 2021;100:877-85. DOI: https://doi.org/10.1159/000515605
Andolfi M, Potenza R, Capozzi R, et al. The role of bronchoscopy in the diagnosis of early lung cancer: a review. J Thorac Dis 2016;8:3329-37. DOI: https://doi.org/10.21037/jtd.2016.11.81

Ethics approval

The study was approved by the Institutional Ethics Committee ( FMIEC/CCM/712/2024 ). The committee assessed the planned project as ethically unobjectionable.

How to Cite



“Diagnostic Utility of Flexible Bronchoscopy in Smear-Negative and Atypical Lung Infections: Identifying Tuberculosis, Fungal, and Non-Tuberculous Mycobacteria Infections and Malignancy”. 2025. Monaldi Archives for Chest Disease, September. https://doi.org/10.4081/monaldi.2025.3562.