Expert consensus on the integrated diagnosis of idiopathic multicentric Castleman disease

Q4 Medicine
Santiago Montes-Moreno , Fina Climent , Máximo Fraga , José Luis Patier , Ángel Robles-Marhuenda , Ramón García-Sanz , Enrique M. Ocio , Andrés González García , José-Tomás Navarro
{"title":"Expert consensus on the integrated diagnosis of idiopathic multicentric Castleman disease","authors":"Santiago Montes-Moreno ,&nbsp;Fina Climent ,&nbsp;Máximo Fraga ,&nbsp;José Luis Patier ,&nbsp;Ángel Robles-Marhuenda ,&nbsp;Ramón García-Sanz ,&nbsp;Enrique M. Ocio ,&nbsp;Andrés González García ,&nbsp;José-Tomás Navarro","doi":"10.1016/j.patol.2022.12.003","DOIUrl":null,"url":null,"abstract":"<div><p>Idiopathic multicentric Castleman disease (iMCD) is rare. The differential diagnosis includes inflammatory, autoimmune and neoplastic disease. The identification of the histopathological features of Castleman disease in the lymph node is the main diagnostic criterion.</p><p>Fifty-three experts from three medical societies (SEMI, SEHH and SEAP) have created a multi-disciplinary consensus document in order to standardise the diagnosis of Castleman disease. Using the Delphi method, specific recommendations for the initial clinical, laboratory and imaging studies have been made for an integrated diagnosis of iMCD as well as for the best way to obtain samples for histopathological confirmation, correct laboratory procedure and interpretation and reporting of results.</p></div>","PeriodicalId":39194,"journal":{"name":"Revista Espanola de Patologia","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista Espanola de Patologia","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S169988552300003X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Idiopathic multicentric Castleman disease (iMCD) is rare. The differential diagnosis includes inflammatory, autoimmune and neoplastic disease. The identification of the histopathological features of Castleman disease in the lymph node is the main diagnostic criterion.

Fifty-three experts from three medical societies (SEMI, SEHH and SEAP) have created a multi-disciplinary consensus document in order to standardise the diagnosis of Castleman disease. Using the Delphi method, specific recommendations for the initial clinical, laboratory and imaging studies have been made for an integrated diagnosis of iMCD as well as for the best way to obtain samples for histopathological confirmation, correct laboratory procedure and interpretation and reporting of results.

特发性多中心Castleman病综合诊断的专家共识
特发性多中心Castleman病(iMCD)是罕见的。鉴别诊断包括炎症性、自身免疫性和肿瘤性疾病。淋巴结中Castleman病的组织病理学特征的识别是主要的诊断标准。来自三个医学会(SEMI、SEHH和SEAP)的五十三名专家创建了一份多学科共识文件,以标准化Castleman病的诊断。使用德尔菲方法,为iMCD的综合诊断以及获取样本以进行组织病理学确认、正确的实验室程序以及结果解释和报告的最佳方式,提出了初步临床、实验室和影像学研究的具体建议。
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
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
×
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