• 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

一名男孩的复发性心包积液:潜在心包和肺淋巴管扩张的线索。

Recurrent pericardial effusion in a boy: A clue to underlying pericardial and pulmonary lymphangiectasia.

作者信息

Bhattacharya Deepanjan, Gopalakrishnan Arun, Sasikumar Deepa, Ayyappan Anoop, Kurup Harikrishnan Kn, Menon Sabarinath, Krishnamoorthy Kavasseri M

机构信息

Department of Cardiology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala, India.

Department of Radiology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala, India.

出版信息

Ann Pediatr Cardiol. 2022 Jul-Aug;15(4):412-414. doi: 10.4103/apc.apc_212_21. Epub 2023 Jan 6.

DOI:10.4103/apc.apc_212_21
PMID:36935824
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10015394/
Abstract

Pulmonary lymphangiectasia is a rare congenital malformation of lymphatic vessels. We report the case of a 5-year-old boy with recurrent pericardial effusion which was diagnosed to be due to pericardial and pulmonary lymphangiectasia.

摘要

肺淋巴管扩张症是一种罕见的淋巴管先天性畸形。我们报告一例5岁男孩反复出现心包积液,经诊断是由心包和肺淋巴管扩张症所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56c5/10015394/ad922a7ba408/APC-15-412-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56c5/10015394/76ca698104ad/APC-15-412-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56c5/10015394/a348340db19b/APC-15-412-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56c5/10015394/ad922a7ba408/APC-15-412-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56c5/10015394/76ca698104ad/APC-15-412-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56c5/10015394/a348340db19b/APC-15-412-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56c5/10015394/ad922a7ba408/APC-15-412-g003.jpg

相似文献

1
Recurrent pericardial effusion in a boy: A clue to underlying pericardial and pulmonary lymphangiectasia.一名男孩的复发性心包积液:潜在心包和肺淋巴管扩张的线索。
Ann Pediatr Cardiol. 2022 Jul-Aug;15(4):412-414. doi: 10.4103/apc.apc_212_21. Epub 2023 Jan 6.
2
Successful thoracic duct embolisation in a child with recurrent massive pericardial effusion diagnosed as a lymphatic anomaly.儿童复发性大量心包积液被诊断为淋巴管异常,经胸导管栓塞治疗成功。
Cardiol Young. 2020 Apr;30(4):571-573. doi: 10.1017/S1047951120000323. Epub 2020 Feb 24.
3
A Rare Case of Chylothorax due to Pulmonary Lymphangiectasia in a 7-Year-Old Boy.一名7岁男孩因肺淋巴管扩张症导致乳糜胸的罕见病例。
European J Pediatr Surg Rep. 2013 Jun;1(1):18-20. doi: 10.1055/s-0033-1337111. Epub 2013 Mar 19.
4
Lymphoscintigraphy In a Case of Recurrent Chylopericardium.复发性乳糜性心包炎病例中的淋巴闪烁显像
Asia Ocean J Nucl Med Biol. 2020 Spring;8(2):157-159. doi: 10.22038/AOJNMB.2020.46512.1311.
5
Complicated chylous pericardial and thoracic effusion as the first clinical manifestation of thoracic lymphatic malformation.复杂的乳糜性心包和胸腔积液作为胸段淋巴管畸形的首发临床表现。
Interact Cardiovasc Thorac Surg. 2020 Apr 1;30(4):654-655. doi: 10.1093/icvts/ivz301.
6
Congenital generalized lymphangiectasia: a rare developmental disorder for non-immune fetal hydrops.先天性全身性淋巴管扩张症:一种导致非免疫性胎儿水肿的罕见发育障碍。
Autops Case Rep. 2015 Dec 30;5(4):27-33. doi: 10.4322/acr.2015.027. eCollection 2015 Oct-Dec.
7
Primary congenital pulmonary lymphangiectasia--a case report.原发性先天性肺淋巴管扩张症——病例报告
Wien Klin Wochenschr. 1997 Dec 12;109(23):922-4.
8
[A case of Hennekam syndrome presenting with massive pericardial effusion].[一例以大量心包积液为表现的亨内坎综合征病例]
Turk Kardiyol Dern Ars. 2008 Jul;36(5):325-8.
9
and gene mutations result in congenital lymphangiectasia in newborns: A case report.基因突导致新生儿先天性淋巴管扩张症:一例报告
World J Clin Cases. 2023 Jul 26;11(21):5179-5186. doi: 10.12998/wjcc.v11.i21.5179.
10
Pleural effusion and ascites in extrarenal lymphangiectasia caused by post-biopsy hematoma: A case report.活检后血肿导致肾外淋巴管扩张症并发胸腔积液和腹水:一例报告
World J Clin Cases. 2020 Dec 26;8(24):6330-6336. doi: 10.12998/wjcc.v8.i24.6330.

本文引用的文献

1
A new classification system for primary lymphatic dysplasias based on phenotype.基于表型的原发性淋巴组织发育不良新分类系统。
Clin Genet. 2010 May;77(5):438-52. doi: 10.1111/j.1399-0004.2010.01394.x.
2
Congenital pulmonary lymphangiectasia.先天性肺淋巴管扩张症
Orphanet J Rare Dis. 2006 Oct 30;1:43. doi: 10.1186/1750-1172-1-43.
3
Pulmonary lymphangiectasia: diagnosis and clinical course.
Pediatr Pulmonol. 2004 Oct;38(4):308-13. doi: 10.1002/ppul.20100.
4
Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.常染色体隐性遗传性肠淋巴管扩张症和淋巴水肿,伴有面部异常和智力发育迟缓。
Am J Med Genet. 1989 Dec;34(4):593-600. doi: 10.1002/ajmg.1320340429.