Cryptogenic bilateral fibrosing pleuritis

D.R. Buchanan , I.D.A. Johnston , I.H. Kerr , M.R. Hetzel , B. Corrin , M. Turner-Warwick
{"title":"Cryptogenic bilateral fibrosing pleuritis","authors":"D.R. Buchanan ,&nbsp;I.D.A. Johnston ,&nbsp;I.H. Kerr ,&nbsp;M.R. Hetzel ,&nbsp;B. Corrin ,&nbsp;M. Turner-Warwick","doi":"10.1016/0007-0971(88)90042-3","DOIUrl":null,"url":null,"abstract":"<div><p>We describe four patients with bilateral pleural effusions progressing to diffuse progressing to diffuse pleural thickening for which we have been unable to find any evidence of an infective, embolic or occupational aetiology. In order to avoid confusion with diffuse pleural thickening attributable to asbestos-related disease, the term cryptogenic bilateral fibrosing pleuritis is suggested.</p><p>The patients differed from those with pleural shadowing due to asbestos in that none of them gave a history of asbestos exposure, all were ill, presented with chest pain which was not always pleuritic in character, and had dyspnoea, cough or malaise. They had pleural effusions of variable size, pleural shadowing radiographically and raised sedimentation rates. Computed tomography revealed bilateral extensive pleural thickening in all cases. All four were HLA B44 positive.</p><p>Histology showed that in all cases the pleura was thickned by fibrous tissue. Both layers were affected and the pleural space was often obliterated. Otherwise the plaural surface was covered by organizing fibrin. Focal collections of lymphocytes were often present when the fibrous tissue abutted on the subpleural fat. No asbestos bodies were seen in any of the cases and in one patient electron microscopic fibre counts showed no excess of asbestos.</p><p>Pleural decortication was successful in three patients. In one of these, contralateral disease was successfully controlled with corticosteroids, but the fourth patient has not improved on corticosteroids.</p></div>","PeriodicalId":75618,"journal":{"name":"British journal of diseases of the chest","volume":"82 ","pages":"Pages 186-193"},"PeriodicalIF":0.0000,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0007-0971(88)90042-3","citationCount":"36","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"British journal of diseases of the chest","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0007097188900423","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 36

Abstract

We describe four patients with bilateral pleural effusions progressing to diffuse progressing to diffuse pleural thickening for which we have been unable to find any evidence of an infective, embolic or occupational aetiology. In order to avoid confusion with diffuse pleural thickening attributable to asbestos-related disease, the term cryptogenic bilateral fibrosing pleuritis is suggested.

The patients differed from those with pleural shadowing due to asbestos in that none of them gave a history of asbestos exposure, all were ill, presented with chest pain which was not always pleuritic in character, and had dyspnoea, cough or malaise. They had pleural effusions of variable size, pleural shadowing radiographically and raised sedimentation rates. Computed tomography revealed bilateral extensive pleural thickening in all cases. All four were HLA B44 positive.

Histology showed that in all cases the pleura was thickned by fibrous tissue. Both layers were affected and the pleural space was often obliterated. Otherwise the plaural surface was covered by organizing fibrin. Focal collections of lymphocytes were often present when the fibrous tissue abutted on the subpleural fat. No asbestos bodies were seen in any of the cases and in one patient electron microscopic fibre counts showed no excess of asbestos.

Pleural decortication was successful in three patients. In one of these, contralateral disease was successfully controlled with corticosteroids, but the fourth patient has not improved on corticosteroids.

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
隐源性双侧纤维化性胸膜炎
我们描述了4例双侧胸膜积液进展为弥漫性进展为弥漫性胸膜增厚的患者,我们无法找到任何感染,栓塞或职业病因的证据。为了避免与可归因于石棉相关疾病的弥漫性胸膜增厚混淆,建议使用隐源性双侧纤维化胸膜炎。这些患者与石棉胸膜阴影患者的不同之处在于,他们都没有石棉暴露史,所有患者都患病,表现为胸痛,但并不总是胸膜炎的特征,并有呼吸困难,咳嗽或不适。他们有不同大小的胸腔积液,胸膜影,沉降率升高。计算机断层扫描显示所有病例双侧广泛胸膜增厚。四人均为HLA B44阳性。组织学显示所有病例胸膜均有纤维组织增厚。两层均受影响,胸膜间隙常被湮没。否则,斑块表面被组织纤维蛋白覆盖。当纤维组织与胸膜下脂肪相接时,常出现局灶性淋巴细胞聚集。在所有病例中均未见石棉体,其中一名患者的电镜纤维计数显示没有过量石棉。胸膜脱屑术成功3例。在其中一个病例中,对侧疾病通过皮质类固醇得到了成功的控制,但第四个患者在皮质类固醇治疗后并没有好转。
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
自引率
0.00%
发文量
0
期刊最新文献
Chronic beryllium disease in identical twins. Induction of bronchial hyperresponsiveness following smoke inhalation injury. Progressive apical pleural fibrosis: a 'constrictive' ventilatory defect. Apical pulmonary fibrosis in psoriasis. Short course chemotherapy for lymph node tuberculosis: final report at 5 years. British Thoracic Society Research Committee.
×
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