中华皮肤科杂志 ›› 2025, e20230345.doi: 10.35541/cjd.20230345

• 研究报道 • 上一篇    下一篇

羟氯喹所致急性泛发性发疹性脓疱病3例基因变异研究

邵依1    张帅1    窦进法1    卞璐1    樊星1    李明2    刘鸿伟1    王建波1    李建国1   

  1. 1河南省人民医院  郑州大学人民医院 河南大学人民医院皮肤科,郑州  450003;2复旦大学儿童医院皮肤科,上海  200032
  • 收稿日期:2023-06-15 修回日期:2024-07-18 发布日期:2025-02-10
  • 通讯作者: 王建波;李建国 E-mail:wangjianbo1020@163.com; drljg006@163.com
  • 基金资助:
    河南省卫生中青年学科带头人培养项目

Genetic variation analysis in three cases of acute generalized exanthematous pustulosis caused by hydroxychloroquine

Shao Yi1, Zhang Shuai1, Dou Jinfa1, Bian Lu1, Fan Xing1, Li Ming2, Liu Hongwei1, Wang Jianbo1, Li Jianguo1   

  1. 1Department of Dermatology, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Henan University People's Hospital, Zhengzhou 450003, China; 2Department of Dermatology, Children's Hospital of Fudan University, Shanghai 200032, China
  • Received:2023-06-15 Revised:2024-07-18 Published:2025-02-10
  • Contact: Wang Jianbo; Li Jianguo E-mail:wangjianbo1020@163.com; drljg006@163.com
  • Supported by:
    Henan Health Young and Middle-aged Discipline Leader Training Project

摘要: 【摘要】 报道3例羟氯喹所致急性泛发性发疹性脓疱病。3例均为女性,年龄23、30、28岁,例1、例3加用羟氯喹治疗系统性红斑狼疮4 d、12 d后出现皮疹,例2早孕8周,加用羟氯喹治疗抗磷脂抗体综合征10 d后出现皮疹。临床均表现为高热,面颈部、躯干、四肢泛发圆形或类圆形水肿性红斑,上有大量针尖大小脓疱,躯干部和双上肢多发多形红斑样病变,可见靶形损害。3例患者均检测出IL36RN基因突变,例1为IL36RN c.115+6T>C纯合突变,父母均为杂合突变携带者;例2从母亲遗传了IL36RN c.115+6T>C杂合突变;例3为IL36RN c.115+6T>C杂合突变,为新生突变。诊断:急性泛发性发疹性脓疱病。治疗:例1和例2在原有基础疾病治疗上加用皮下注射阿达木单抗治疗,1周后皮损明显消退;例3应用大剂量糖皮质激素治疗,4周后皮损消退;例1和例2未见明显不良反应,例3后期出现股骨头坏死。随访42个月,3例患者均未出现皮损反复,例2在治疗8个月后产下1名健康男婴。

关键词: 急性泛发性发疹性脓疱病, 羟氯喹, IL36RN基因, 阿达木单抗注射液

Abstract: 【Abstract】 To report 3 cases of acute generalized exanthematous pustulosis (AGEP) caused by hydroxychloroquine. All three patients were females, aged 23, 30, and 28 years respectively. In cases 1 and 3, the rashes appeared 4 days and 12 days after the treatment with hydroxychloroquine for systemic lupus erythematosus; case 2, who was 8 weeks pregnant, developed rashes 10 days after starting hydroxychloroquine treatment for antiphospholipid syndrome. All the 3 patients had high fever, and clinically presented with generalized round or oval-shaped edematous erythema on the face, neck, trunk and limbs, covered with a large number of pinhead-sized pustules, and with multiple erythema multiforme-like lesions on the trunk and both upper limbs, including targetoid lesions. Mutations in the IL36RN gene were identified in all the 3 patients: a homozygous mutation c.115+6T>C in the IL36RN gene was found in case 1, and her parents were heterozygous carriers; case 2 inherited the heterozygous mutation c.115+6T>C in the IL36RN gene from her mother; the heterozygous mutation c.115+6T>C found in case 3 was a de novo mutation. A diagnosis of AGEP was made. Cases 1 and 2 received subcutaneous injections of adalimumab in addition to the treatment of their underlying diseases, and skin lesions markedly regressed after 1 week of treatment; case 3 was treated with high-dose glucocorticoids, and lesions subsided after 4 weeks; no significant adverse reactions were observed in cases 1 and 2, however, femoral head necrosis was noted in case 3. During a follow-up period of 42 months, none of the patients experienced a recurrence, and case 2 gave birth to a healthy baby boy after 8-month treatment.

Key words: Acute Generalized Exanthematous Pustulosis, Hydroxychloroquine, IL36RN gene, Adalimumab

引用本文

邵依 张帅 窦进法 卞璐 樊星 李明 刘鸿伟 王建波 李建国. 羟氯喹所致急性泛发性发疹性脓疱病3例基因变异研究[J]. 中华皮肤科杂志, 2025,e20230345. doi:10.35541/cjd.20230345

Shao Yi, Zhang Shuai, Dou Jinfa, Bian Lu, Fan Xing, Li Ming, Liu Hongwei, Wang Jianbo, Li Jianguo. Genetic variation analysis in three cases of acute generalized exanthematous pustulosis caused by hydroxychloroquine[J]. Chinese Journal of Dermatology,2025,e20230345. doi:10.35541/cjd.20230345