Amiodarone-induced pulmonary toxicity can rarely present as unilateral pulmonary fibrosis, requiring high clinical suspicion for timely diagnosis and drug withdrawal.
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.
Wagle et al. (Sun,) studied this question.