Li C W, Sun N, Li S N, Zhang Y C, Ma J J
Department of Rheumatology & Clinical Immunology, Tianjin Children's Hospital, Tianjin 300134, China.
Zhonghua Er Ke Za Zhi. 2024 Nov 2;62(11):1103-1107. doi: 10.3760/cma.j.cn112140-20240813-00577.
To summarize the clinical features and outcomes of deflazacort-induced Steven Johnson syndrome (SJS)-toxic epidermal necrolysis (TEN) to raise awareness among patients with Duchenne muscular dystrophy (DMD), neurologists as well as other deflazacort users. The clinical data of a boy with DMD who had SJS induced by deflazacort treated at the Department of Rheumatology & Clinical Immunology of Tianjin Children's Hospital in July 2024 was analyzed retrospectively. Taking "deflazacort" "Steven-Johnson syndrome" "toxic epidermal necrolysis" in Chinese or English as the keywords, literature was searched at CNKI, Wanfang, China Biomedical Literature Database and PubMed up to July 2024. The clinical characteristics, treatment and outcomes of deflazacort-induced SJS-TEN were summarized. A 12-year-old boy was admitted with a 3-day history of rash. He was diagnosed with DMD at the age of 3 and had been treated with prednisolone since the age of 8. Forty-four days before admission, the patient started deflazacort to replace prednisolone. Three days before admission, progressively worsening erythematous maculopapular rashes, blisters and skin peeling (8% body surface area), oral mucosal erosion, and exudative conjunctivitis occurred, thus deflazacort was discontinued. Complete remission of SJS was achieved after treatment with intravenous immunoglobulin (IVIG, total 1.4 g/kg), 2 doses of etanercept (0.9 mg/kg, once), subcutaneous injection and intravenous methylprednisolone (0.7 mg/(kg·d)). Based on the literature, there were 5 reports in English while none in Chinese, altogether 7 cases were reported. All the patients were male, aged 3-45 years. Duration of deflazacort exposure was 2-8 weeks. Dermatology diagnosis of our case was SJS, and 5 cases were TEN. One patient was diagnosed with exudative erythema multiforme, and subsequent deflazacort oral challenge test was positive. Treatment included methylprednisolone or dexamethasone in 5 cases, IVIG in 6 cases, etanercept in 3 cases and cyclosporine in 1 case. All patients recovered completely. The synthetic corticosteroid deflazacort can cause rare but severe adverse reactions such as SJS-TEN, which needs close monitoring and prompt recognition and management.
总结地夫可特诱发的史蒂文斯-约翰逊综合征(SJS)-中毒性表皮坏死松解症(TEN)的临床特征及转归,以提高杜氏肌营养不良症(DMD)患者、神经科医生以及其他地夫可特使用者的认识。回顾性分析2024年7月在天津市儿童医院风湿免疫科接受治疗的1例因服用地夫可特诱发SJS的DMD男孩的临床资料。以中文或英文的“地夫可特”“史蒂文斯-约翰逊综合征”“中毒性表皮坏死松解症”为关键词,检索截至2024年7月的中国知网、万方、中国生物医学文献数据库和PubMed数据库中的文献。总结地夫可特诱发SJS-TEN的临床特征、治疗方法及转归。1例12岁男孩因皮疹3天入院。他3岁时被诊断为DMD,8岁起接受泼尼松龙治疗。入院前44天,患者开始用地夫可特替代泼尼松龙。入院前3天,出现逐渐加重的红斑丘疹、水疱及皮肤剥脱(体表面积8%)、口腔黏膜糜烂和渗出性结膜炎,因此停用了地夫可特。经静脉注射免疫球蛋白(IVIG,总量1.4 g/kg)、2剂依那西普(0.9 mg/kg,单次)皮下注射及静脉注射甲泼尼龙(0.7 mg/(kg·d))治疗后,SJS完全缓解。根据文献,英文报道有5例,中文报道无,共报道7例。所有患者均为男性,年龄3 - 45岁。地夫可特暴露时间为2 - 8周。本例经皮肤科诊断为SJS,5例为TEN。1例患者诊断为渗出性多形红斑,随后地夫可特口服激发试验呈阳性。治疗方法包括5例使用甲泼尼龙或地塞米松,6例使用IVIG,3例使用依那西普,1例使用环孢素。所有患者均完全康复。合成糖皮质激素地夫可特可引起罕见但严重的不良反应,如SJS-TEN,需要密切监测、及时识别和处理。