Subcutaneous apomorphine-induced pneumonitis: An uncommon pulmonary adverse event

IF 0.7 Q4 RESPIRATORY SYSTEM
Respiratory Medicine Case Reports Pub Date : 2026-01-01 Epub Date: 2026-06-04 DOI:10.1016/j.rmcr.2026.102446
Enrique Barrueco-Otero, Vanesa Hidalgo-Sierra, Patricia Torres Piñero, Isabel González Fernández, Laura Gil Pintor, María Bartol Sánchez, María Jesús Corbi Cobo-Losey, Carlos Montilla, Miguel Ángel Hernández-Mezquita
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引用次数: 0

Abstract

Introduction

Apomorphine is a potent dopaminergic agonist widely used in the management of motor fluctuations in advanced Parkinson's disease. Although generally well tolerated, rare pulmonary adverse drug reactions (ADRs) may occur. We report a case of probable apomorphine-induced pneumonitis associated with subcutaneous administration.

Case presentation

A 62-year-old Caucasian male with multiple comorbidities presented to the emergency department with headache, non-productive cough, central chest pain, fever, and dyspnea over the past 48 hours (3 weeks after initiation of subcutaneous apomorphin). Chest X-ray revealed bilateral hilar infiltrates and basal consolidation. CT scan showed organizing pneumonia (OP)-like pattern. Extensive microbiological evaluation of bronchoalveolar lavage and bronchial aspirate samples, including bacterial, fungal, mycobacterial, viral, and atypical pathogen testing, was negative. Lack of response to broad-spectrum antibiotics raised the suspicion of drug-induced pneumonitis due to subcutaneous apomorphine. Antibiotics were discontinued, and corticosteroid therapy (methylprednisolone 40 mg/day) was initiated with gradual tapering resulted in rapid clinical improvement and complete radiological resolution within one month.

Conclusion

The temporal relationship between apomorphine initiation and symptom onset, compatible clinical and radiological findings, extensive microbiological exclusion of infectious causes, and favorable response after drug withdrawal and corticosteroid therapy supported the diagnosis of probable apomorphine-induced pneumonitis.
阿帕吗啡诱发的皮下肺炎:一种罕见的肺部不良事件。
阿波啡是一种有效的多巴胺能激动剂,广泛用于治疗晚期帕金森病的运动波动。虽然一般耐受性良好,但可能会发生罕见的肺部药物不良反应(adr)。我们报告一例可能的阿帕吗啡引起的肺炎与皮下给药有关。病例介绍:一名62岁白人男性,患有多种合并症,在过去48小时内(开始皮下阿帕啡3周后)出现头痛、非咳、中枢性胸痛、发烧和呼吸困难。胸部x线显示双侧肺门浸润及基底实变。CT表现为组织性肺炎(OP)样。支气管肺泡灌洗和支气管吸入样本的广泛微生物学评估,包括细菌、真菌、分枝杆菌、病毒和非典型病原体检测,均为阴性。对广谱抗生素缺乏反应,引起了对皮下阿帕吗啡引起的药物性肺炎的怀疑。停用抗生素,并开始皮质类固醇治疗(甲基强的松龙40mg /天),逐渐减量导致临床快速改善,并在一个月内完全放射消退。结论:阿波吗啡起始与症状发作的时间关系、符合临床和影像学表现、广泛的微生物学排除感染原因、停药和皮质类固醇治疗后的良好反应支持阿波吗啡所致肺炎的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports RESPIRATORY SYSTEM-
CiteScore
2.10
自引率
0.00%
发文量
213
审稿时长
87 days
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