Amiodarone-Induced Pulmonary Toxicity Presenting as Unilateral Fibrosis: A Case Report

Amiodarone-induced pulmonary toxicity (APT) is a potentially life-threatening complication that most commonly presents as bilateral interstitial lung disease. This case highlights a rare presentation of APT manifesting as unilateral pulmonary fibrosis, posing a diagnostic challenge. An 86-year-old man on long-term amiodarone presented with gradually worsening dyspnea and cough. Chest imaging demonstrated pleural thickening, peripheral opacities, and fibrotic changes confined entirely to the left lung. A broad evaluation, including infectious studies, autoimmune testing, hypersensitivity panels, and bronchoscopy with lavage, did not identify another etiology. Amiodarone was promptly discontinued, and corticosteroid therapy was initiated, resulting in clinical improvement. This case highlights an atypical presentation of APT as unilateral pulmonary fibrosis, which can complicate timely diagnosis due to its asymmetrical radiographic features. Early recognition and withdrawal of amiodarone are essential to limit progression to irreversible fibrosis.

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Publication Details

Journal
Cureus
Published
2026-01-04
DOI
https://doi.org/10.7759/cureus.100729
Citations
1
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
36.44
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Amiodarone-Induced Pulmonary Toxicity Presenting as Unilateral Fibrosis: A Case Report

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1 citations
Cureus
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
36.44
article

Amiodarone-Induced Pulmonary Toxicity Presenting as Unilateral Fibrosis: A Case Report

Dharana Gelal, Aavash Mishra, Vikas Pathak, Anuj Timshina, Sishir Poudel, Laxman Wagle
article en
1 citations

Abstract

Amiodarone-induced pulmonary toxicity (APT) is a potentially life-threatening complication that most commonly presents as bilateral interstitial lung disease. This case highlights a rare presentation of APT manifesting as unilateral pulmonary fibrosis, posing a diagnostic challenge. An 86-year-old man on long-term amiodarone presented with gradually worsening dyspnea and cough. Chest imaging demonstrated pleural thickening, peripheral opacities, and fibrotic changes confined entirely to the left lung. A broad evaluation, including infectious studies, autoimmune testing, hypersensitivity panels, and bronchoscopy with lavage, did not identify another etiology. Amiodarone was promptly discontinued, and corticosteroid therapy was initiated, resulting in clinical improvement. This case highlights an atypical presentation of APT as unilateral pulmonary fibrosis, which can complicate timely diagnosis due to its asymmetrical radiographic features. Early recognition and withdrawal of amiodarone are essential to limit progression to irreversible fibrosis.

CureusVol. 18(1)
Saint Agnes Hospital (US), Good Samaritan Hospital (US), KIST Medical College (NP), Pulmonary and Critical Care Associates (US), B.P. Koirala Institute of Health Sciences (NP)
Openalex Percentile: Top 2%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
36.44
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