Valproic acid-induced Stevens-Johnson syndrome

D. V. Somov, Alina Y Chernyaeva, Veronika A Mazus, Lyamam T Nurieva, Maksim A. Bobrov, D. A. Anichkov
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Abstract

A 27-year-old transgender female at the stage of gender transition with bipolar disorder for which she received valproic acid developed multiple petechial rashes on the chest, upper and lower extremities, local erythematous lesions with forming blisters, large-platelet peeling on the face, neck, chest and inguinal area, erosion on the oral mucosa. She was diagnosed with drug eruption, Stevens-Johnson syndrome. The diagnosis was verified on the basis of complaints, medical history, clinical picture, laboratory findings. Treatment included dexamethasone, infusion therapy, vancomycin, cyclosporine A, valproic acid withdrawal. Against the background of the therapy, skin condition was improved: there was the epithelization of ulcerative defects and the absence of new elements.
丙戊酸诱发史蒂文斯-约翰逊综合征
一名 27 岁的变性女性,正处于性别转换阶段,患有双相情感障碍,曾服用丙戊酸治疗,胸部、上肢和下肢出现多处瘀点状皮疹,局部红斑伴水疱形成,面部、颈部、胸部和腹股沟区出现大面积血小板脱落,口腔黏膜糜烂。她被诊断为药物性糜烂、史蒂文斯-约翰逊综合征。诊断是根据主诉、病史、临床表现和实验室检查结果核实的。治疗包括地塞米松、输液治疗、万古霉素、环孢素 A、丙戊酸停药。在治疗的背景下,皮肤状况有所改善:溃疡性缺损上皮化,没有新的元素。
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