Report of Hidradenitis Suppurativa in an Individual Affected by Rubinstein-Taybi Syndrome.

IF 1.2 4区 医学 Q3 DERMATOLOGY
Erik J Wanberg, Kathleen M Fletcher, Nessa Aghazadeh Mohandesi, Afsaneh Alavi
{"title":"Report of Hidradenitis Suppurativa in an Individual Affected by Rubinstein-Taybi Syndrome.","authors":"Erik J Wanberg, Kathleen M Fletcher, Nessa Aghazadeh Mohandesi, Afsaneh Alavi","doi":"10.1111/pde.15906","DOIUrl":null,"url":null,"abstract":"<p><p>Rubinstein-Taybi syndrome (RTS) is a rare genetic disorder featuring craniofacial abnormalities, intellectual disability, and multi-organ involvement, including increased risk of keloid formation, pilomatricomas, and hypertrichosis. Hidradenitis suppurativa (HS), a chronic inflammatory skin condition characterized by recurrent abscess formation and draining tunnels, has never been described in a patient affected by RTS. In this report, we detail the history of a 32-year-old male with RTS and refractory Hurley stage III HS and discuss the important considerations and risks of managing this unique patient population.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2000,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Dermatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/pde.15906","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Rubinstein-Taybi syndrome (RTS) is a rare genetic disorder featuring craniofacial abnormalities, intellectual disability, and multi-organ involvement, including increased risk of keloid formation, pilomatricomas, and hypertrichosis. Hidradenitis suppurativa (HS), a chronic inflammatory skin condition characterized by recurrent abscess formation and draining tunnels, has never been described in a patient affected by RTS. In this report, we detail the history of a 32-year-old male with RTS and refractory Hurley stage III HS and discuss the important considerations and risks of managing this unique patient population.

鲁宾斯坦-泰比综合征1例化脓性汗腺炎报告。
鲁宾斯坦-泰比综合征(RTS)是一种罕见的遗传性疾病,以颅面异常、智力残疾和多器官受累为特征,包括瘢痕疙瘩形成、毛瘤瘤和多毛症的风险增加。化脓性汗腺炎(HS)是一种慢性炎症性皮肤病,以复发性脓肿形成和引流隧道为特征,从未在RTS患者中被描述过。在本报告中,我们详细介绍了一名32岁男性RTS合并难治性Hurley III期HS的病史,并讨论了处理这一独特患者群体的重要注意事项和风险。
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
Pediatric Dermatology
Pediatric Dermatology 医学-皮肤病学
CiteScore
3.20
自引率
6.70%
发文量
269
审稿时长
1 months
期刊介绍: Pediatric Dermatology answers the need for new ideas and strategies for today''s pediatrician or dermatologist. As a teaching vehicle, the Journal is still unsurpassed and it will continue to present the latest on topics such as hemangiomas, atopic dermatitis, rare and unusual presentations of childhood diseases, neonatal medicine, and therapeutic advances. As important progress is made in any area involving infants and children, Pediatric Dermatology is there to publish the findings.
×
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:481959085
Book学术官方微信