A clinical case of a combination of rheumatoid arthritis that debuted with the development of bronchiectasis

The article presents a description of a clinical case of rheumatoid arthritis (RA) that debuted with the development of bronchiectasis (BE) without symptoms of systemic disease. The course of the disease was characterized by insufficient effectiveness of standard therapy for BE and frequent exacerbations of the disease that had no obvious cause. Clinical symptoms of RA appeared 5 years after the onset of the disease. The article also provides a review of the literature on the pulmonary manifestations of RA and the relationship between the pathogenetic mechanisms of RA and BE.

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Publication Details

Journal
Journal of Respiratory Medicine
Published
2026-07-02
DOI
https://doi.org/10.17116/respmed2026202156
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
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article

A clinical case of a combination of rheumatoid arthritis that debuted with the development of bronchiectasis

S. Yu. Chikina, A. V. Kuleshov
Journal of Respiratory Medicine
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

A clinical case of a combination of rheumatoid arthritis that debuted with the development of bronchiectasis

S. Yu. Chikina, A. V. Kuleshov
article en

Abstract

The article presents a description of a clinical case of rheumatoid arthritis (RA) that debuted with the development of bronchiectasis (BE) without symptoms of systemic disease. The course of the disease was characterized by insufficient effectiveness of standard therapy for BE and frequent exacerbations of the disease that had no obvious cause. Clinical symptoms of RA appeared 5 years after the onset of the disease. The article also provides a review of the literature on the pulmonary manifestations of RA and the relationship between the pathogenetic mechanisms of RA and BE.

Journal of Respiratory MedicineVol. 2(2)
Sechenov University (RU), Integrative Medicine Institute (US)
Good health and well-being
Openalex Percentile: Top 8%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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