卡马西平治疗过程中Steven Johnson综合征与伴有嗜酸性粒细胞增多和全身症状的皮疹重叠

IF 0.2 Q4 DERMATOLOGY
O. Mohammed, Abdelrahman Osman, P. Amirthalingam, Amirah M Alatawi, H. Mirghani, Wajdi Hashim Elseed Mohamed
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引用次数: 0

摘要

Stevens-Johnson综合征(SJS)和伴有嗜酸性粒细胞增多和全身症状的皮疹(DRESS)是一系列严重皮肤药物不良反应的一部分。区分这两种综合征是谨慎的,因为治疗和预后不同。卡马西平是SJS和DRESS常见的罪魁祸首药物之一。本病例研究的对象是一名45岁的印度尼西亚妇女,她在卡马西平治疗后出现非典型SJS。然而,区分SJS和DRESS是至关重要的。此外,卡马西平诱导的SJS与南亚人群中特定的人类白细胞抗原等位基因密切相关。此后,该病例强调了区分SJS和DRESS的重要性,并证实了其他研究,这些研究强烈建议在易感人群中开始使用卡马西平之前检测人类白细胞抗原等位基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overlapping of Steven-Johnson syndrome and the drug rash with eosinophilia and systemic symptoms during the treatment of carbamazepine
The Stevens-Johnson syndrome (SJS) and the drug rash with eosinophilia and systemic symptoms (DRESS) are part of a spectrum of severe adverse cutaneous drug reactions. It is prudent to differentiate between the two syndromes, as the management and prognosis are different. Carbamazepine is one of the common culprit drugs for both SJS and DRESS. This case study is of a 45-year-old Indonesian women who developed atypical presentation of SJS following carbamazepine therapy. However, it is essential to distinguish between the SJS and DRESS. Moreover, carbamazepine-induced SJS is strongly linked to specific human leukocyte antigen alleles in the South Asian people. Henceforth, this case emphasizes the importance of differentiating SJS from DRESS and substantiates other studies that strongly recommend testing for human leukocyte antigen alleles before initiating carbamazepine in a susceptible population.
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