• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肺泡蛋白沉积症与终末期肺纤维化:一种罕见的关联。

Pulmonary alveolar proteinosis and end-stage pulmonary fibrosis: a rare association.

作者信息

Agarwal Prachi P, Seely Jean M, Perkins D Garth, Matzinger Fred R, Alikhan Qasim

机构信息

Department of Diagnostic Imaging, The Ottawa Hospital, Ottawa, Ontario, Canada.

出版信息

J Thorac Imaging. 2005 Aug;20(3):242-4. doi: 10.1097/01.rti.0000160733.74997.2d.

DOI:10.1097/01.rti.0000160733.74997.2d
PMID:16077345
Abstract

We present the high resolution CT features of marked pulmonary fibrosis in a patient known to have pulmonary alveolar proteinosis (PAP) confirmed on open lung biopsy. Significant fibrosis in PAP is an extremely rare occurrence with only a few case reports. Our case demonstrated a predominantly central distribution, which has not been described previously.

摘要

我们展示了一名经开胸肺活检确诊为肺泡蛋白沉积症(PAP)患者显著肺纤维化的高分辨率CT特征。PAP中出现显著纤维化极为罕见,仅有少数病例报告。我们的病例显示主要为中央分布,这在之前未曾有过描述。

相似文献

1
Pulmonary alveolar proteinosis and end-stage pulmonary fibrosis: a rare association.肺泡蛋白沉积症与终末期肺纤维化:一种罕见的关联。
J Thorac Imaging. 2005 Aug;20(3):242-4. doi: 10.1097/01.rti.0000160733.74997.2d.
2
Pulmonary alveolar proteinosis with interstitial involvement.伴有间质受累的肺泡蛋白沉积症。
AJR Am J Roentgenol. 1981 Nov;137(5):1069-71. doi: 10.2214/ajr.137.5.1069.
3
Pulmonary interstitial fibrosis following alveolar proteinosis.肺泡蛋白沉积症后发生的肺间质纤维化。
Chest. 1974 Jun;65(6):700-2. doi: 10.1378/chest.65.6.700.
4
Relationship between diffuse pulmonary fibrosis, alveolar proteinosis, and granulocyte-macrophage colony stimulating factor autoantibodies.弥漫性肺纤维化、肺泡蛋白沉积症和粒细胞-巨噬细胞集落刺激因子自身抗体之间的关系。
Respir Care. 2011 Oct;56(10):1608-10. doi: 10.4187/respcare.01054. Epub 2011 Apr 19.
5
Pulmonary Fibrosis on High-Resolution CT of Patients With Pulmonary Alveolar Proteinosis.肺泡蛋白沉积症患者高分辨率CT上的肺纤维化
AJR Am J Roentgenol. 2016 Sep;207(3):544-51. doi: 10.2214/AJR.15.14982.
6
A case of uncomplicated pulmonary alveolar proteinosis evolving to pulmonary fibrosis.一例单纯型肺泡蛋白沉积症演变为肺纤维化的病例。
Monaldi Arch Chest Dis. 2007 Dec;67(4):234-7. doi: 10.4081/monaldi.2007.480.
7
Pulmonary interstitial fibrosis associated with alveolar proteinosis.与肺泡蛋白沉积症相关的肺间质纤维化
Thorax. 1983 Nov;38(11):865-6. doi: 10.1136/thx.38.11.865.
8
[A case of pulmonary alveolar proteinosis associated with fibrotic changes and alveolitis].[一例合并纤维化改变及肺泡炎的肺泡蛋白沉积症]
Nihon Kyobu Shikkan Gakkai Zasshi. 1989 Oct;27(10):1214-20.
9
[A rare cause of diffuse interstitial pneumopathy: alveolar proteinosis (apropos of a case)].[弥漫性间质性肺病的罕见病因:肺泡蛋白沉积症(附病例报告)]
Tunis Med. 1998 Feb;76(2):1085-8.
10
Lung cancer may develop subsequently or coincidently with pulmonary alveolar proteinosis.肺癌可能随后发生,或与肺泡蛋白沉积症同时发生。
Lung Cancer. 2007 Oct;58(1):144-8. doi: 10.1016/j.lungcan.2007.04.012. Epub 2007 Jun 13.

引用本文的文献

1
The dark side of pulmonary alveolar proteinosis.肺泡蛋白沉积症的阴暗面
Multidiscip Respir Med. 2025 Jul 21;20(1):1027. doi: 10.5826/mrm.2025.1027.
2
Pulmonary Alveolar Proteinosis-associated Pulmonary Fibrosis: Evolutional Changes and Radiologic-Pathologic Correlation.肺泡蛋白沉积症相关的肺纤维化:演变过程及影像学-病理学相关性
Radiol Cardiothorac Imaging. 2023 Oct 19;5(5):e230040. doi: 10.1148/ryct.230040. eCollection 2023 Oct.
3
Autoimmune Pulmonary Alveolar Proteinosis.自身免疫性肺含铁血黄素沉着症。
Am J Respir Crit Care Med. 2022 May 1;205(9):1016-1035. doi: 10.1164/rccm.202112-2742SO.
4
Pulmonary alveolar proteinosis: from classification to therapy.肺泡蛋白沉积症:从分类到治疗
Breathe (Sheff). 2020 Jun;16(2):200018. doi: 10.1183/20734735.0018-2020.
5
CT findings in pulmonary alveolar proteinosis: serial changes and prognostic implications.肺泡蛋白沉积症的CT表现:系列变化及预后意义
J Thorac Dis. 2018 Oct;10(10):5774-5783. doi: 10.21037/jtd.2018.09.86.
6
Role of granulocyte-macrophage colony-stimulating factor in pulmonary fibrosis following pulmonary alveolar proteinosis.粒细胞-巨噬细胞集落刺激因子在肺泡蛋白沉积症后肺纤维化中的作用。
Respirol Case Rep. 2016 May 5;4(4):e00159. doi: 10.1002/rcr2.159. eCollection 2016 Jul.
7
Primary pulmonary alveolar proteinosis: computed tomography features at diagnosis.原发性肺泡蛋白沉积症:诊断时的计算机断层扫描特征
Pediatr Radiol. 2014 Jul;44(7):795-802. doi: 10.1007/s00247-014-2888-1. Epub 2014 Mar 6.
8
Congenital pulmonary alveolar proteinosis.先天性肺泡蛋白沉积症。
Case Rep Pediatr. 2013;2013:764216. doi: 10.1155/2013/764216. Epub 2013 Apr 27.
9
Pulmonary alveolar proteinosis in children: a case series.儿童肺泡蛋白沉积症:病例系列
J Res Med Sci. 2010 Mar;15(2):120-4.
10
Pulmonary alveolar proteinosis in workers at an indium processing facility.铟加工厂工人的肺泡蛋白质沉积症。
Am J Respir Crit Care Med. 2010 Mar 1;181(5):458-64. doi: 10.1164/rccm.200907-1022CR. Epub 2009 Dec 17.