Anuntrangsee Tanaporn, Chanprapaph Kumutnart, Iamsumang Wimolsiri
Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Clin Cosmet Investig Dermatol. 2024 Oct 28;17:2409-2415. doi: 10.2147/CCID.S489028. eCollection 2024.
D-penicillamine is used as the mainstay of chelation therapy for Wilson's disease and for heavy metal intoxication. D-penicillamine itself has been noted to cause several systemic side effects as well as symptoms related to the skin. Common cutaneous side effects such as acute hypersensitivity reactions, elastic fiber abnormalities, and bullous diseases have been occasionally described. Herein, we report a case of a 23-year-old Thai female with gold intoxication who developed Stevens-Johnson syndrome (SJS) following the treatment of D-penicillamine. To our knowledge, D-penicillamine-induced SJS is exceptionally rare. To raise awareness of potentially fatal cutaneous adverse drug reaction triggered by D-penicillamine, published literature regarding SJS induced by this agent has also been reviewed. D-penicillamine should be regarded as a possible culprit in patients presenting with SJS following D-penicillamine administration and should be promptly discontinued.
青霉胺是用于肝豆状核变性和重金属中毒螯合疗法的主要药物。青霉胺本身已被注意到会引起多种全身副作用以及与皮肤相关的症状。常见的皮肤副作用,如急性过敏反应、弹性纤维异常和大疱性疾病,偶尔也有描述。在此,我们报告一例23岁泰国女性金中毒患者,在接受青霉胺治疗后发生了史蒂文斯-约翰逊综合征(SJS)。据我们所知,青霉胺诱发的SJS极为罕见。为提高对青霉胺引发的潜在致命性皮肤药物不良反应的认识,我们还回顾了关于该药物诱发SJS的已发表文献。对于在服用青霉胺后出现SJS的患者,应将青霉胺视为可能的罪魁祸首,并应立即停药。