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新发传染病电子杂志 ›› 2026, Vol. 11 ›› Issue (2): 66-70.doi: 10.19871/j.cnki.xfcrbzz.2026.02.013

• 病例报道 • 上一篇    下一篇

左氧氟沙星抗结核治疗致中毒性表皮坏死松解症1例报道

胡少瑜1,2, 冯艳仪1, 戚振红2   

  1. 1.佛山市第四人民医院结核科,广东 佛山 528200;
    2.广州中医药大学第八临床医学院,广东 佛山 528200
  • 收稿日期:2025-07-28 出版日期:2026-04-30 发布日期:2026-05-18
  • 通讯作者: 戚振红,Email:qizhenhong82@163.com
  • 基金资助:
    1.佛山市科学技术局2023年自筹经费类科技创新项目培育项目(2320001006800); 2.2024年度佛山市卫生健康局医学科研项目(20240720A010635)

A case report of toxic epidermal necrolysis induced by levofloxacin during anti-tuberculosis treatment

Hu Shaoyu1,2, Feng Yanyi1, Qi Zhenhong2   

  1. 1. Department of Tuberculosis, Foshan Fourth People's Hospital, Guangdong Foshan, 528200, China;
    2. The Eighth Clinical Medical College of Guangzhou University of Chinese Medicine, Guangdong Foshan, 528200, China
  • Received:2025-07-28 Online:2026-04-30 Published:2026-05-18

摘要: 本文报道1例因使用左氧氟沙星进行抗结核治疗引起中毒性表皮坏死松解症(toxic epidermal necrolysis,TEN)的病例。患者肺癌治疗后并发活动性肺结核,后出现了由抗结核药物诱发的罕见而致命的TEN。诊疗上立即停用可疑药物,使用表皮坏死松解症药物因果关系算法分析,确认左氧氟沙星为致病药物,TEN严重程度评分评估患者病死率达62%。治疗团队联用糖皮质激素、免疫球蛋白、TNF-α拮抗剂治疗TEN,同时启动强效的二线抗结核治疗,有效降低免疫治疗诱发结核菌播散的风险。在TEN痊愈后,治疗团队实施了药物激发试验,验证了患者对异烟肼、乙胺丁醇、吡嗪酰胺的耐受性,并以此制定后续的抗结核方案。本病例不仅警示了左氧氟沙星导致TEN的罕见严重风险,也为肺结核合并TEN的诊疗提供参考。

关键词: 中毒性表皮坏死松解症, 结核病, 左氧氟沙星

Abstract: This report describes a case of levofloxacin-induced toxic epidermal necrolysis (TEN) occurring during antituberculosis therapy. A patient developed active pulmonary tuberculosis following treatment for lung cancer and subsequently experienced a rare and potentially fatal case of toxic epidermal necrolysis induced by anti-tuberculosis drugs. In clinical management, suspicious medications were immediately discontinued, and an analysis using the Algorithm of Drug Causality for Epidermal Necrolysis identified levofloxacin as the causative drug. The Severity-of-Illness Score for Toxic Epidermal Necrolysis estimated the patient's mortality risk at 62%. To manage TEN, the treatment team initiated a combination of corticosteroids, immunoglobulins, and TNF-α antagonists, while concurrently starting intensive second-line anti-tuberculosis therapy. This approach effectively reduced the risk of tuberculosis dissemination triggered by immunotherapy. Following the resolution of TEN, a drug provocation test was performed to evaluate the patient's tolerance to isoniazid, ethambutol, and pyrazinamide, which subsequently informed the formulation of a revised anti-tuberculosis regimen. This case underscores the rare and severe risk of TEN induced by levofloxacin and provides valuable insights into the management of pulmonary tuberculosis complicated by TEN.

Key words: Toxic epidermal necrolysis, Tuberculosis, Levofloxacin

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