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头孢呋辛诱导的史蒂文斯-约翰逊综合征后发生闭塞性细支气管炎

Bronchiolitis Obliterans After Cefuroxime-Induced Stevens-Johnson Syndrome.

作者信息

Shabrawishi Mohammed, Qanash Sultan A

机构信息

Department of Inernal Medicine, King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia.

Department of Inernal Medicine, King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Jeddah, Saudi Arabia.

出版信息

Am J Case Rep. 2019 Feb 9;20:171-174. doi: 10.12659/AJCR.913723.

Abstract

BACKGROUND Bronchiolitis obliterans is the term used to describe a clinical syndrome of irreversible airflow obstruction. Among the etiologies linked to this entity is the rarely reported association with Stevens-Johnson syndrome, which has had a poor outcome in most of the previously published cases. The optimum management of bronchiolitis obliterans as a complication of Stevens-Johnson syndrome is not well defined. CASE REPORT A 41-year-old woman developed significant shortness of breath 3 months after recovering from Stevens-Johnson syndrome precipitated by a second-generation cephalosporin. She was found to have severe irreversible airway obstruction on physiology studies, and computed tomography scans of the inspiratory and expiratory phases of respiration showed air trapping that was more prominent on expiratory films. The patient was diagnosed with bronchiolitis obliterans, for which bronchodilators and long-term macrolide therapy were administered. Although she did not recover completely, her follow-up physiology studies showed that the bronchiolitis obliterans was stable. CONCLUSIONS Bronchiolitis obliterans secondary to Stevens-Johnson syndrome is a rare entity that is progressive and can lead to functional impairment. Identifying the disease at an early stage might stabilize or slow its progression. Herein, we describe a case of bronchiolitis obliterans as a complication of Stevens-Johnson syndrome and review the literature to raise awareness of this condition, highlight its course, and discuss the available treatments.

摘要

背景 闭塞性细支气管炎是用于描述不可逆气流阻塞临床综合征的术语。与该病症相关的病因中,有一种是与史蒂文斯-约翰逊综合征的关联,这种关联很少被报道,且在大多数已发表的病例中预后较差。作为史蒂文斯-约翰逊综合征并发症的闭塞性细支气管炎的最佳治疗方法尚不明确。病例报告 一名41岁女性在因第二代头孢菌素引发的史蒂文斯-约翰逊综合征康复3个月后出现明显气短。生理检查发现她存在严重的不可逆气道阻塞,呼吸吸气期和呼气期的计算机断层扫描显示存在空气潴留,呼气期影像上更为明显。该患者被诊断为闭塞性细支气管炎,给予支气管扩张剂和长期大环内酯类药物治疗。尽管她未完全康复,但随访生理检查显示闭塞性细支气管炎病情稳定。结论 史蒂文斯-约翰逊综合征继发的闭塞性细支气管炎是一种罕见的、进行性的病症,可导致功能损害。早期识别该疾病可能会使其病情稳定或减缓进展。在此,我们描述一例史蒂文斯-约翰逊综合征并发症所致的闭塞性细支气管炎病例,并回顾文献以提高对该病症的认识,突出其病程,并讨论可用的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a96d/6380208/82a7db3503f2/amjcaserep-20-171-g001.jpg

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