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美罗培南:嗜酸性粒细胞性肺疾病中一个可能的新病因。

Meropenem: A possible new culprit in eosinophilic lung diseases.

作者信息

Hatem Nathalie Abi, Campbell Sabrina, Rubio Edmundo, Loschner Anthony Lukas

机构信息

Department of Pulmonary, Critical Care, Environmental and Sleep Medicine, Roanoke, USA.

出版信息

Lung India. 2017 Sep-Oct;34(5):461-464. doi: 10.4103/lungindia.lungindia_328_16.

Abstract

Eosinophilic lung diseases are a diverse group of pulmonary disorders with an extensive list of differential diagnoses. Multiple drugs particularly antibiotics can cause pulmonary eosinophilia with variable pulmonary manifestations. Cutaneous drug reactions are common. Diagnosis is usually made on clinical history and blood eosinophilia with an accumulation of eosinophils in alveolar spaces on histologic analysis. Imaging findings are nonspecific. Stopping the offending agent is often enough while a short course of corticosteroids can hasten recovery. We present a unique case of eosinophilic pneumonia due to meropenem that highlights the importance of keeping a low threshold of suspicion regarding the etiology of drug-induced lung diseases as the current list is not exhaustive, and new agents are being identified continuously. A 51-year-old African American woman presented with fever, dyspnea, and diffuse pustular rash. She had been treated with meropenem intravenously through a peripherally inserted central catheter for 6 weeks before presentation for Pseudomonas aeruginosa septic arthritis of the left knee. She had a temperature of 102.2 F and SpO2of 86% on room air. Chest roentgenogram had scattered infiltrates and chest tomography showed bilateral ground-glass opacities. Laboratory workup showed peripheral eosinophilia. Bronchoalveolar lavage revealed a white blood cell of 2230 with 89% eosinophils. Skin lesions' biopsies showed pustular dermatosis, compatible with acute drug-induced eosinophilic lung disease with skin involvement. As meropenem was the only medication she had been exposed to, it was stopped and systemic steroids were initiated with improvement in respiratory and clinical status and complete recovery on follow-up.

摘要

嗜酸性粒细胞性肺疾病是一组多样的肺部疾病,鉴别诊断范围广泛。多种药物尤其是抗生素可导致肺嗜酸性粒细胞增多,并伴有多种肺部表现。皮肤药物反应很常见。诊断通常基于临床病史、血液嗜酸性粒细胞增多以及组织学分析显示肺泡腔内嗜酸性粒细胞聚集。影像学表现不具有特异性。停用致病药物通常就足够了,而短期使用皮质类固醇可以加速恢复。我们报告了一例由美罗培南引起的嗜酸性粒细胞性肺炎的独特病例,强调了对药物性肺病病因保持低怀疑阈值的重要性,因为目前的清单并不详尽,并且不断有新的药物被发现。一名51岁的非裔美国女性出现发热、呼吸困难和弥漫性脓疱疹。在因左膝铜绿假单胞菌败血症性关节炎就诊前,她通过外周静脉置入中心静脉导管接受了6周的美罗培南静脉治疗。她体温为102.2°F,室内空气中SpO2为86%。胸部X线片有散在浸润影,胸部CT显示双侧磨玻璃样混浊。实验室检查显示外周血嗜酸性粒细胞增多。支气管肺泡灌洗显示白细胞计数为2230,其中嗜酸性粒细胞占89%。皮肤病变活检显示脓疱性皮炎,符合伴有皮肤受累的急性药物性嗜酸性粒细胞性肺病。由于美罗培南是她唯一接触过的药物,故停用该药并开始使用全身性类固醇,患者呼吸和临床状况改善,随访时完全康复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dd2/5592760/170436055d20/LI-34-461-g001.jpg

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