Allopurinol-induced DRESS syndrome in the elderly: an exceptional form of iatrogenesis

S. Bouomrani, F. Rekik, S. Trabelsi, S. Yahyaoui, N. Belgacem
{"title":"Allopurinol-induced DRESS syndrome in the elderly: an exceptional form of iatrogenesis","authors":"S. Bouomrani, F. Rekik, S. Trabelsi, S. Yahyaoui, N. Belgacem","doi":"10.25082/AGPM.2019.01.002","DOIUrl":null,"url":null,"abstract":"Introduction The Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) syndrome is a very rare iatrogenic accident that is characterized by its difficult diagnosis due to its clinical latency and heterogeneous clinic. The form induced by allopurinol remains exceptional and often ignored by clinicians, although potentially fatal. We are reporting an original observation of allopurinol-induced DRESS syndrome in elderly. Observation A 64-year-old woman who had been treated with allopurinol for gout for three weeks, was hospitalized for a diffuse, erythematous and maculopapular cutaneous rash, associated with fever at 39°C, dyspnea, generalized lymphadenopathy, and a hyperkeratotic and desquamative plantar eruption. The biology showed eosinophilia at 860/mm3 and cytolitic hepatitis without cholestasis or hepatocellular insufficiency with ASAT at 230 IU/l and alanine aminotransferase ( ALAT) at 280 IU/l. The infectious, immunological investigation, as well as the search for underlying malignant neoplasia or hematological malignancy were negative. The skin biopsy was inconclusive. The diagnosis of a DRESS syndrome induced by allopurinol was retained. The evolution was rapidly favorable after stopping allopurinol and treatment with systemic glucocorticoids. Conclusion The incidence of cutaneous reactions to allopurinol is estimated at 1.5/100,000 H/year. The DRESS syndrome, the most serious form of these reactions, remains exceptional. This particular form of toxicity deserves to be known by clinicians, especially since allopurinol is widely prescribed in the elderly.","PeriodicalId":71557,"journal":{"name":"全科医学进展(英文)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"全科医学进展(英文)","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.25082/AGPM.2019.01.002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction The Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) syndrome is a very rare iatrogenic accident that is characterized by its difficult diagnosis due to its clinical latency and heterogeneous clinic. The form induced by allopurinol remains exceptional and often ignored by clinicians, although potentially fatal. We are reporting an original observation of allopurinol-induced DRESS syndrome in elderly. Observation A 64-year-old woman who had been treated with allopurinol for gout for three weeks, was hospitalized for a diffuse, erythematous and maculopapular cutaneous rash, associated with fever at 39°C, dyspnea, generalized lymphadenopathy, and a hyperkeratotic and desquamative plantar eruption. The biology showed eosinophilia at 860/mm3 and cytolitic hepatitis without cholestasis or hepatocellular insufficiency with ASAT at 230 IU/l and alanine aminotransferase ( ALAT) at 280 IU/l. The infectious, immunological investigation, as well as the search for underlying malignant neoplasia or hematological malignancy were negative. The skin biopsy was inconclusive. The diagnosis of a DRESS syndrome induced by allopurinol was retained. The evolution was rapidly favorable after stopping allopurinol and treatment with systemic glucocorticoids. Conclusion The incidence of cutaneous reactions to allopurinol is estimated at 1.5/100,000 H/year. The DRESS syndrome, the most serious form of these reactions, remains exceptional. This particular form of toxicity deserves to be known by clinicians, especially since allopurinol is widely prescribed in the elderly.
别嘌呤醇诱导的老年人DRESS综合征:一种特殊形式的医源性
引言嗜酸性粒细胞增多症和系统症状综合征(DRESS)是一种非常罕见的医源性事故,由于其临床潜伏期和临床异质性,其特点是诊断困难。别嘌醇诱导的形式仍然是特殊的,通常被临床医生忽视,尽管可能致命。我们报道了一项在老年人中由别嘌呤醇引起的DRESS综合征的原始观察结果。观察一名64岁的女性,接受别嘌醇治疗痛风三周,因弥漫性红斑和斑丘疹住院,伴有39°C的发烧、呼吸困难、全身淋巴结病以及角化过度和足底脱屑性皮疹。生物学显示嗜酸性粒细胞增多症为860/mm3,无胆汁淤积或肝细胞功能不全的细胞性肝炎,ASAT为230IU/l,丙氨酸氨基转移酶(ALAT)为280IU/l。感染、免疫学调查以及潜在恶性肿瘤或血液系统恶性肿瘤的搜索均为阴性。皮肤活检没有结论。别嘌醇诱发的DRESS综合征的诊断保留。在停止别嘌醇和全身糖皮质激素治疗后,进展迅速有利。结论别嘌醇皮肤反应的发生率估计为1.5/10万H/年。DRESS综合征是这些反应中最严重的一种,仍然是例外。这种特殊形式的毒性值得临床医生了解,特别是因为别嘌呤醇在老年人中被广泛使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信