[薯蓣-橙皮苷诱导的DRESS综合征:疱疹病毒的免疫再激活]。

Nataly Flores-García, Carlos Correa-Serrano, Juan Carlos Cardenas-Favela, Diana Cadenas-García, Rosalaura Villarreal-González
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引用次数: 0

摘要

背景:药物反应伴嗜酸性粒细胞增多和全身症状(DRESS)是一种严重的皮肤不良反应。发病率为100 - 100万,死亡率为3.8% -10%,是一种与单纯疱疹病毒再活化有关的疾病。病例报告:一名34岁女性,特应性和静脉功能不全,面部和手臂出现瘙痒性荨麻疹,并发展为麻疹样皮疹、面部水肿、发烧、淋巴结病和脱屑。全血细胞计数未见异常:AST: 837 U/L, ALT: 11352 U/L。由于怀疑为DRESS综合征,开始使用皮质类固醇治疗并进行活检。经询问,患者报告在皮疹发作前21天服用了薯蓣皂苷-橙皮苷并进行了全身防晒(Heliocare360°®)。组织病理学检查显示表皮萎缩,空泡变性,炎症浸润。全身性皮质类固醇治疗三周,疗效满意。2个月后,患者再次出现皮肤病和高转氨酶血症;自身抗体和血清学均为单纯疱疹病毒IgM阳性。结论:本病例强调需要考虑严重的超敏反应,即使使用常用和明显低风险的药物。强调综合方法的重要性,包括确定可疑药物,排除鉴别诊断,延长临床随访时间,并监测可能的病毒再激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Diosmin-hesperidin-induced DRESS syndrome: immune reactivation by herpesvirus].

Background: Drug reaction with eosinophilia and systemic symptoms (DRESS) is a severe cutaneous adverse reaction. The incidence is 1-1,000,000 with a mortality rate of 3.8-10%, and it is a disease associated with reactivation of the herpes simplex virus.

Case report: A 34-year-old woman with atopy and venous insufficiency presented with pruritic hives on her face and arms, which progressed to a morbilliform rash, facial edema, fever, lymphadenopathy, and scaling. A complete blood count showed no abnormalities: AST: 837 U/L, ALT: 11352 U/L. Due to the suspicion of DRESS syndrome, treatment with corticosteroids was initiated and a biopsy was obtained. Upon questioning, the patient reported having taken diosmin-hesperidin and undergone systemic sunscreen (Heliocare360°®) 21 days prior to the onset of the rash. Histopathological examination revealed atrophic epidermis, vacuolar degeneration, and inflammatory infiltrate. Systemic corticosteroids were administered for three weeks, with a satisfactory response. Two months later, the patient experienced reactivation of the dermatosis and hypertransaminasemia; the autoantibody panel and serology were positive for IgM for herpes simplex virus.

Conclusion: This case underscores the need to consider severe hypersensitivity reactions, even with commonly used and apparently low-risk drugs. The importance of a comprehensive approach, including identification of the suspected medication, exclusion of differential diagnoses, prolonged clinical follow-up, and surveillance for possible viral reactivation, is emphasized.

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