Dapsone Induced Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) Syndrome - A Case Report

S. Ali, O. M. Ibrahim, S. Abdalla
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Abstract

A 50-year-old male Sudanese patient presented with a three-week history of jaundice, high-grade fever, and mucocutaneous eruption. For last months he was on compound therapy for leprosy, which had been confirmed recently. The patient’s face was prominent, along with the erythematous dusky morbilliform rash covering all the body. On examination, we detected hepatosplenomegaly and generalized lymphadenopathy. Laboratory investigations revealed hepatorenal impairment, and hematological analysis revealed leukocytosis mainly due to eosinophilia. The clinical and laboratory findings interpretation ranked DRESS or Drug-Induced Hypersensitivity Syndrome (DIHS) on top of possible causes before Dapsone Hypersensitivity Syndrome (DHS) and lepra reactions. We promptly discontinued MDT, admitted him to the dermatological ward. Two skin biopsies were sent to two different histopathologists, MF was suggested by one and Sezary syndrome by the other one. Besides the general conservative measures and vital functions monitoring, he received systemic and topical steroids. However, unfortunately, within the next three weeks, his condition deteriorated, and passed away from multi-systems failure.
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氨苯砜致药物性皮疹伴嗜酸性粒细胞增多和全身症状(DRESS)综合征1例报告
一名50岁苏丹男性患者,有三周黄疸、高热和皮肤粘膜疹史。在过去的几个月里,他一直在接受麻风病的综合治疗,最近才被确诊。患者面部突出,全身有暗色的麻疹样红斑。在检查中,我们发现肝脾肿大和全身性淋巴结病。实验室检查显示肝肾损害,血液学分析显示主要由嗜酸性粒细胞增多引起的白细胞增多。临床和实验室结果解释将DRESS或药物性超敏反应综合征(DIHS)排在氨苯砜超敏反应综合征(DHS)和麻风反应之前的可能原因。我们立即停止了MDT治疗,让他住进了皮肤科病房。两份皮肤活检被送到两个不同的组织病理学家,一个建议MF,另一个建议Sezary综合征。除常规保守措施和生命功能监测外,患者接受全身和局部类固醇治疗。然而,不幸的是,在接下来的三周内,他的病情恶化,并离开了多系统故障。
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