致命血管炎病例的尸检结果

Diagnostic Histopathology Pub Date : 2025-01-01 Epub Date: 2024-11-02 DOI:10.1016/j.mpdhp.2024.10.007
Richard John Digby, Hannah Olivia Hawrot
{"title":"致命血管炎病例的尸检结果","authors":"Richard John Digby,&nbsp;Hannah Olivia Hawrot","doi":"10.1016/j.mpdhp.2024.10.007","DOIUrl":null,"url":null,"abstract":"<div><div>The term “vasculitis” refers to a family of conditions characterized by inflammation of blood vessels. These processes can affect small, medium or large vessels, and have a wide range of clinical presentations, histological appearances, and prognoses. As histopathologists, we usually see these vasculitides in a partially or well-treated state; patients have often commenced local or systemic therapy by the time of their biopsy, and this can significantly affect the histological appearances. This case report describes the clinical history and associations of a fatal case of granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis. GPA is an uncommon multisystem vasculitis, classically involving the respiratory tract and kidneys, though other systems are also known to be affected including the GI tract, skin, and joints among many others. The post-mortem examination identified the immediate cause of death, and demonstrated very well the typical histological features that may be observed in this condition.</div></div>","PeriodicalId":39961,"journal":{"name":"Diagnostic Histopathology","volume":"31 1","pages":"Pages 39-41"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Post-mortem findings in a case of fatal vasculitis\",\"authors\":\"Richard John Digby,&nbsp;Hannah Olivia Hawrot\",\"doi\":\"10.1016/j.mpdhp.2024.10.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The term “vasculitis” refers to a family of conditions characterized by inflammation of blood vessels. These processes can affect small, medium or large vessels, and have a wide range of clinical presentations, histological appearances, and prognoses. As histopathologists, we usually see these vasculitides in a partially or well-treated state; patients have often commenced local or systemic therapy by the time of their biopsy, and this can significantly affect the histological appearances. This case report describes the clinical history and associations of a fatal case of granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis. GPA is an uncommon multisystem vasculitis, classically involving the respiratory tract and kidneys, though other systems are also known to be affected including the GI tract, skin, and joints among many others. The post-mortem examination identified the immediate cause of death, and demonstrated very well the typical histological features that may be observed in this condition.</div></div>\",\"PeriodicalId\":39961,\"journal\":{\"name\":\"Diagnostic Histopathology\",\"volume\":\"31 1\",\"pages\":\"Pages 39-41\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Diagnostic Histopathology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1756231724001701\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/2 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diagnostic Histopathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1756231724001701","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/2 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

“血管炎”一词是指一系列以血管炎症为特征的病症。这些病变可影响小、中、大血管,具有广泛的临床表现、组织学表现和预后。作为组织病理学家,我们通常看到这些血管血管处于部分或良好的状态;患者通常在活检时开始局部或全身治疗,这可以显著影响组织学表现。本病例报告描述了一个致命的肉芽肿病合并多血管炎(GPA)的临床病史和关联,以前称为韦格纳肉芽肿病。GPA是一种罕见的多系统血管炎,通常累及呼吸道和肾脏,尽管已知其他系统也会受到影响,包括胃肠道、皮肤和关节等。尸检确定了死亡的直接原因,并很好地证明了在这种情况下可能观察到的典型组织学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Post-mortem findings in a case of fatal vasculitis
The term “vasculitis” refers to a family of conditions characterized by inflammation of blood vessels. These processes can affect small, medium or large vessels, and have a wide range of clinical presentations, histological appearances, and prognoses. As histopathologists, we usually see these vasculitides in a partially or well-treated state; patients have often commenced local or systemic therapy by the time of their biopsy, and this can significantly affect the histological appearances. This case report describes the clinical history and associations of a fatal case of granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis. GPA is an uncommon multisystem vasculitis, classically involving the respiratory tract and kidneys, though other systems are also known to be affected including the GI tract, skin, and joints among many others. The post-mortem examination identified the immediate cause of death, and demonstrated very well the typical histological features that may be observed in this condition.
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
Diagnostic Histopathology
Diagnostic Histopathology Medicine-Pathology and Forensic Medicine
CiteScore
1.30
自引率
0.00%
发文量
64
期刊介绍: This monthly review journal aims to provide the practising diagnostic pathologist and trainee pathologist with up-to-date reviews on histopathology and cytology and related technical advances. Each issue contains invited articles on a variety of topics from experts in the field and includes a mini-symposium exploring one subject in greater depth. Articles consist of system-based, disease-based reviews and advances in technology. They update the readers on day-to-day diagnostic work and keep them informed of important new developments. An additional feature is the short section devoted to hypotheses; these have been refereed. There is also a correspondence section.
期刊最新文献
Editorial board The spectrum of cerebral amyloid angiopathy-related inflammation The pathological diagnosis of nerve biopsies: a practical approach A case of meningeal solitary fibrous tumour with papillary morphology Molecular glioblastoma: high-grade malignancy with low-grade histomorphology
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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