• 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

弯刀状等等——形态异常的右肺。

Scimitar etcetera--the dysmorphic right lung.

作者信息

Partridge J B, Osborne J M, Slaughter R E

机构信息

Department of Medical Imaging, Killingbeck Hospital, Leeds.

出版信息

Clin Radiol. 1988 Jan;39(1):11-9. doi: 10.1016/s0009-9260(88)80329-5.

DOI:10.1016/s0009-9260(88)80329-5
PMID:3338237
Abstract

'Dysmorphic lung' is introduced as a term to describe any complex congenital malformation which involves both abnormal vascular morphology and disordered growth of a whole lung. The major group within this definition is the scimitar syndrome, which we choose to mean a hypoplastic lung with anomalous venous drainage and various degrees of collateral arterial supply. Nine typical cases of scimitar are presented, with three closely related cases. Six other cases of dysmorphic lungs are also present. The relationships between the groups are discussed, and an effort is made to clarify the nomenclature used in this condition.

摘要

“畸形肺”是一个术语,用于描述任何涉及异常血管形态和全肺生长紊乱的复杂先天性畸形。该定义中的主要类型是弯刀综合征,我们将其定义为伴有异常静脉引流和不同程度侧支动脉供应的肺发育不全。本文展示了9例典型的弯刀综合征病例,以及3例密切相关的病例。还展示了其他6例畸形肺病例。讨论了各病例组之间的关系,并努力阐明该病症中使用的命名法。

相似文献

1
Scimitar etcetera--the dysmorphic right lung.弯刀状等等——形态异常的右肺。
Clin Radiol. 1988 Jan;39(1):11-9. doi: 10.1016/s0009-9260(88)80329-5.
2
Variants of the scimitar syndrome.弯刀综合征的变异型。
Cardiol Young. 2016 Jun;26(5):941-7. doi: 10.1017/S1047951115001651. Epub 2015 Sep 16.
3
[Anomalous venous drainage of the hypoplastic right lung and other malformations (scimitar syndrome)].[发育不全右肺的异常静脉引流及其他畸形(弯刀综合征)]
Rev Clin Esp. 1976 Sep 30;142(6):581-6.
4
The crossover lung segment: congenital malformation associated with a variant of scimitar syndrome.交叉肺段:与弯刀综合征变异型相关的先天性畸形。
Thorax. 1987 Jun;42(6):417-9. doi: 10.1136/thx.42.6.417.
5
Scimitar sign with normal pulmonary venous drainage and systemic arterial supply. Scimitar syndrome or bronchopulmonary sequestration?伴有正常肺静脉引流和体循环动脉供血的弯刀征。是弯刀综合征还是肺隔离症?
Chest. 1994 Jan;105(1):294-5. doi: 10.1378/chest.105.1.294.
6
Scimitar syndrome: experience with 6 patients.弯刀综合征:6例患者的经验
Asian Cardiovasc Thorac Ann. 2009 Jun;17(3):266-71. doi: 10.1177/0218492309104750.
7
Scimitar syndrome: A rare case of recurrent pneumonia.弯刀综合征:一例复发性肺炎的罕见病例。
J Pak Med Assoc. 2019 Mar;69(3):423-425.
8
[Scimitar syndrome with horseshoe lung (author's transl)].弯刀综合征合并肺叶融合(作者译)
Rofo. 1982 Mar;136(3):265-9. doi: 10.1055/s-2008-1056044.
9
The relationship between scimitar syndrome, so-called scimitar variant, meandering right pulmonary vein, horseshoe lung and pulmonary arterial sling.镰刀综合征、所谓的镰刀状变异、蜿蜒右肺静脉、马蹄肺与肺动脉吊带之间的关系。
Cardiol Young. 2006 Jun;16(3):300-4. doi: 10.1017/S1047951106000461.
10
Retrocardiac lung lobe in a neonate with Scimitar syndrome.患有弯刀综合征的新生儿的心后肺叶。
Pediatr Pulmonol. 2017 Sep;52(9):E49-E51. doi: 10.1002/ppul.23701. Epub 2017 Apr 3.

引用本文的文献

1
A systematic classification of the congenital bronchopulmonary vascular malformations: dysmorphogeneses of the primitive foregut system and the primitive aortic arch system.先天性支气管肺血管畸形的系统分类:原始前肠系统和原始主动脉弓系统的发育异常
Yonsei Med J. 2008 Feb 29;49(1):90-102. doi: 10.3349/ymj.2008.49.1.90.
2
Isolated and complex scimitar vein anomalies and their differentiation from the meandering right pulmonary vein.孤立性和复杂性弯刀状静脉异常及其与蜿蜒走行的右肺静脉的鉴别
Yonsei Med J. 2007 Dec 31;48(6):973-80. doi: 10.3349/ymj.2007.48.6.973.
3
The dysmorphic lung: imaging findings.
畸形肺:影像学表现
Eur Radiol. 1996;6(4):403-14. doi: 10.1007/BF00182451.
4
Scimitar syndrome associated with partial anomalous pulmonary venous connection at the supracardiac, cardiac, and infracardiac levels.弯刀综合征合并心上型、心内型和心下型部分性肺静脉异位连接。
Pediatr Cardiol. 1993 Oct;14(4):234-7. doi: 10.1007/BF00795378.