前列腺炎是肉芽肿合并多血管炎的最初表现。

Q3 Medicine
Nauman Ismat Butt, Raheel Younus, Muhammad Qasim Khan Tareen, Sumaira Farman, Nighat Mir Ahmad, Amna Ahmad
{"title":"前列腺炎是肉芽肿合并多血管炎的最初表现。","authors":"Nauman Ismat Butt,&nbsp;Raheel Younus,&nbsp;Muhammad Qasim Khan Tareen,&nbsp;Sumaira Farman,&nbsp;Nighat Mir Ahmad,&nbsp;Amna Ahmad","doi":"10.55519/JAMC-04-S4-10658","DOIUrl":null,"url":null,"abstract":"<p><p>Granulomatosis with polyangiitis (GPA) is an uncommon pauci-immune small-vessel necrotising granulomatous vasculitis mostly seen in age 45-60 years. We present the case of a formerly healthy 44 years old male presenting with dysuria and intermittent urinary retention for 8 months, not responding to empirical antibiotic therapy and TURP. A prostate biopsy showed necrotising granulomatous prostatitis. Urinalysis demonstrated persistent pyuria and haematuria, but cultures showed no growth. Subsequently he complained of fever, cough, dyspnoea and skin ulcers. CT of the chest showed multiple cavitatory lesions and pleural effusion. On work up, c-ANCA was positive and a diagnosis of granulomatosis with polyangiitis was established. This depicts a rarely seen presentation of prostatitis as the initial feature of GPA.</p>","PeriodicalId":15141,"journal":{"name":"Journal of Ayub Medical College, Abbottabad : JAMC","volume":"34(Suppl 1) 4","pages":"S1043-S1045"},"PeriodicalIF":0.0000,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prostatitis As An Initial Presentation For Granulomatosis With Polyangiitis.\",\"authors\":\"Nauman Ismat Butt,&nbsp;Raheel Younus,&nbsp;Muhammad Qasim Khan Tareen,&nbsp;Sumaira Farman,&nbsp;Nighat Mir Ahmad,&nbsp;Amna Ahmad\",\"doi\":\"10.55519/JAMC-04-S4-10658\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Granulomatosis with polyangiitis (GPA) is an uncommon pauci-immune small-vessel necrotising granulomatous vasculitis mostly seen in age 45-60 years. We present the case of a formerly healthy 44 years old male presenting with dysuria and intermittent urinary retention for 8 months, not responding to empirical antibiotic therapy and TURP. A prostate biopsy showed necrotising granulomatous prostatitis. Urinalysis demonstrated persistent pyuria and haematuria, but cultures showed no growth. Subsequently he complained of fever, cough, dyspnoea and skin ulcers. CT of the chest showed multiple cavitatory lesions and pleural effusion. On work up, c-ANCA was positive and a diagnosis of granulomatosis with polyangiitis was established. This depicts a rarely seen presentation of prostatitis as the initial feature of GPA.</p>\",\"PeriodicalId\":15141,\"journal\":{\"name\":\"Journal of Ayub Medical College, Abbottabad : JAMC\",\"volume\":\"34(Suppl 1) 4\",\"pages\":\"S1043-S1045\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Ayub Medical College, Abbottabad : JAMC\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.55519/JAMC-04-S4-10658\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Ayub Medical College, Abbottabad : JAMC","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55519/JAMC-04-S4-10658","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

肉芽肿病合并多血管炎(GPA)是一种罕见的少免疫小血管坏死性肉芽肿性血管炎,多见于45-60岁。我们提出一个病例,以前健康的44岁男性表现为排尿困难和间歇性尿潴留8个月,没有响应经验抗生素治疗和TURP。前列腺活检显示坏死性肉芽肿性前列腺炎。尿液分析显示持续脓尿和血尿,但培养未见生长。随后他主诉发烧、咳嗽、呼吸困难和皮肤溃疡。胸部CT显示多发空化灶及胸腔积液。在工作中,c-ANCA阳性,诊断为肉芽肿病合并多血管炎。图示罕见的前列腺炎为GPA的初始特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prostatitis As An Initial Presentation For Granulomatosis With Polyangiitis.

Granulomatosis with polyangiitis (GPA) is an uncommon pauci-immune small-vessel necrotising granulomatous vasculitis mostly seen in age 45-60 years. We present the case of a formerly healthy 44 years old male presenting with dysuria and intermittent urinary retention for 8 months, not responding to empirical antibiotic therapy and TURP. A prostate biopsy showed necrotising granulomatous prostatitis. Urinalysis demonstrated persistent pyuria and haematuria, but cultures showed no growth. Subsequently he complained of fever, cough, dyspnoea and skin ulcers. CT of the chest showed multiple cavitatory lesions and pleural effusion. On work up, c-ANCA was positive and a diagnosis of granulomatosis with polyangiitis was established. This depicts a rarely seen presentation of prostatitis as the initial feature of GPA.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
0.80
自引率
0.00%
发文量
304
×
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