Trichodysplasia Spinulosa.

Q3 Medicine Sultan Qaboos University Medical Journal Pub Date : 2024-02-01 Epub Date: 2024-02-28 DOI:10.18295/squmj.5.2023.035
Ayida Al Khalili, Elsa Maciagowski, Khue Nguyen, Kevin A Watters
{"title":"Trichodysplasia Spinulosa.","authors":"Ayida Al Khalili, Elsa Maciagowski, Khue Nguyen, Kevin A Watters","doi":"10.18295/squmj.5.2023.035","DOIUrl":null,"url":null,"abstract":"<p><p>Trichodysplasia spinulosa (TS) is a unique, rare clinical and histological dermatologic entity described mainly in a setting of immunosuppression. It is caused by a novel human polymoavirus, TS-associated polyomavirus. Reduction of immunosuppression and/or anti-viral therapy is the main therapeutic strategies used to treat such cases. We report a biopsy-proven case of TS in a male renal transplant patient who presented to a dermatology outpatient clinic in Montreal, Canada, in 2015. He was managed with valgancyclovir with no obvious response. Subsequently, a trial of topical imiquimod was commenced. Awareness of TS can prompt early diagnosis and management to prevent possible complications.</p>","PeriodicalId":22083,"journal":{"name":"Sultan Qaboos University Medical Journal","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10906767/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sultan Qaboos University Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18295/squmj.5.2023.035","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/2/28 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Trichodysplasia spinulosa (TS) is a unique, rare clinical and histological dermatologic entity described mainly in a setting of immunosuppression. It is caused by a novel human polymoavirus, TS-associated polyomavirus. Reduction of immunosuppression and/or anti-viral therapy is the main therapeutic strategies used to treat such cases. We report a biopsy-proven case of TS in a male renal transplant patient who presented to a dermatology outpatient clinic in Montreal, Canada, in 2015. He was managed with valgancyclovir with no obvious response. Subsequently, a trial of topical imiquimod was commenced. Awareness of TS can prompt early diagnosis and management to prevent possible complications.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
毛发育不良
棘毛发育不良(TS)是一种独特的、罕见的临床和组织学皮肤病,主要在免疫抑制的情况下描述。它是由一种新型的人类多瘤病毒引起的,即毛发育不良棘突相关多瘤病毒(TSPyV)。我们报告了2015年在加拿大蒙特利尔皮肤科门诊就诊的一名肾移植患者经活检证实的TS病例。减少免疫抑制和/或抗病毒治疗是治疗此类病例的主要治疗策略。我们的患者接受了缬甘西洛韦治疗,但没有明显的反应。随后,开始了局部咪喹莫特的试验。对TS的认识可以促进早期诊断和管理,以防止可能的并发症。关键词:棘毛发育不良,免疫抑制,器官移植,人类多瘤病毒。
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 去求助
来源期刊
CiteScore
2.00
自引率
0.00%
发文量
86
审稿时长
7 weeks
期刊最新文献
18th Asian Federation of Sports Medicine Congress cum 8th ISN international Sports Medicine & Sports Science Conference: Sabah International Convention Centre, Kota Kinabalu, Sabah, Malaysia, 26-28 April 2024. Blastic Plasmacytoid Dendritic Cell Neoplasm. Re: Efficacy and Safety of Vildagliptin and Remogliflozin as Add-on Therapy to Metformin in Patients of Type 2 Diabetes Mellitus. Short-term Weight Loss Outcomes of 104 Mini Gastric Bypass or One Anastomosis Gastric Bypass Operations A Case of Mirizzi Syndrome with Pancreatic Divisum
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1