• 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

单侧先天性肺发育不全伴血管异常。

Unilateral congenital dysplasia of lung associated with vascular anomalies.

作者信息

Hislop A, Sanderson M, Reid L

出版信息

Thorax. 1973 Jul;28(4):435-41. doi: 10.1136/thx.28.4.435.

DOI:10.1136/thx.28.4.435
PMID:4741444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC470055/
Abstract

, , 435-441. In three cases of unilateral lung dysplasia the structural changes have been analysed quantitatively to throw light on the nature of the anomaly and stage of its appearance. In one case the pulmonary artery was hypoplastic and the systemic supply normal but increased, suggesting onset in late intrauterine life or early childhood: in the other two cases the blood supply was only systemic, from both normal and abnormal arteries, suggesting onset in the early weeks of intrauterine development. Airway development was consistent with this interpretation. All cases had additional signs of maldevelopment of mesodermal tissue. The origin of the various types of systemic artery is discussed.

摘要

,,435 - 441。在三例单侧肺发育不良病例中,对结构变化进行了定量分析,以阐明异常的性质及其出现阶段。在一例中,肺动脉发育不全,体循环供血正常但增加,提示在子宫内晚期或幼儿期发病:在另外两例中,血液供应仅来自体循环,包括正常和异常动脉,提示在子宫内发育的早期几周发病。气道发育与这一解释一致。所有病例都有中胚层组织发育不良的其他体征。讨论了各种类型体循环动脉的起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/a517a0fc5337/thorax00130-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/792349f61e38/thorax00130-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/a3a47052cee6/thorax00130-0037-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/1ba5f5768660/thorax00130-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/8a53e5fcf728/thorax00130-0038-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/a517a0fc5337/thorax00130-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/792349f61e38/thorax00130-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/a3a47052cee6/thorax00130-0037-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/1ba5f5768660/thorax00130-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/8a53e5fcf728/thorax00130-0038-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605a/470055/a517a0fc5337/thorax00130-0039-a.jpg

相似文献

1
Unilateral congenital dysplasia of lung associated with vascular anomalies.单侧先天性肺发育不全伴血管异常。
Thorax. 1973 Jul;28(4):435-41. doi: 10.1136/thx.28.4.435.
2
Unilateral pulmonary hypoplasia associated with complex vascular anomalies.单侧肺发育不全合并复杂血管异常。
Monaldi Arch Chest Dis. 1993 Dec;48(6):620-2.
3
Isolated absence of the right pulmonary artery as a cause of massive hemoptysis.孤立性右肺动脉缺如作为大量咯血的病因
Interact Cardiovasc Thorac Surg. 2008 Dec;7(6):1183-5. doi: 10.1510/icvts.2008.180430. Epub 2008 Sep 5.
4
Bullous lung disease and bronchiectasis in unilateral absent right pulmonary artery.
Gen Thorac Cardiovasc Surg. 2013 Feb;61(2):100-3. doi: 10.1007/s11748-012-0107-2. Epub 2012 Jun 15.
5
Test and teach. Number eighty eight: alveolar capillary dysplasia.检测与讲授。第八十八号:肺泡毛细血管发育不良。
Pathology. 1998 May;30(2):155, 205-6.
6
Neonatal pneumonectomy for isolated unilateral pulmonary artery agenesis.
Ann Thorac Surg. 1991 Aug;52(2):294-5. doi: 10.1016/0003-4975(91)91356-z.
7
Radiographic evaluation of lung abnormalities.
Radiol Clin North Am. 1972 Aug;10(2):333-48.
8
Alveolar capillary dysplasia: a six-year single center experience.肺泡毛细血管发育不良:六年单中心经验
J Perinat Med. 2005;33(4):347-52. doi: 10.1515/JPM.2005.067.
9
Anomalous systemic arterial supply to normal basal segments of the left lung without sequestration.左肺正常基底段存在异常体循环动脉供血且无肺隔离症。
Eur J Cardiothorac Surg. 2015 Mar;47(3):578. doi: 10.1093/ejcts/ezu209. Epub 2014 May 22.
10
Bronchoscopic Findings in Congenital Isolated Unilateral Pulmonary Vein Atresia in an Adult.成人先天性孤立性单侧肺静脉闭锁的支气管镜检查结果
J Bronchology Interv Pulmonol. 2015 Jul;22(3):244-7. doi: 10.1097/LBR.0000000000000171.

本文引用的文献

1
Congenital absence of the right pulmonary artery; diagnosis by angiocardiography, with cardiorespiratory studies.先天性右肺动脉缺如;通过心血管造影及心肺研究进行诊断。
N Engl J Med. 1952 Jul 31;247(5):149-57. doi: 10.1056/NEJM195207312470501.
2
Observations on the anatomy of the intrasegmental bronchial tree.关于节段内支气管树解剖结构的观察
Thorax. 1952 Mar;7(1):89-97. doi: 10.1136/thx.7.1.89.
3
Unilateral lung transradiancy.单侧肺透亮度增加
Thorax. 1962 Sep;17(3):230-9. doi: 10.1136/thx.17.3.230.
4
CONGENITAL ABSENCE OR HYPOPLASIA OF PULMONARY ARTERY.先天性肺动脉缺如或发育不全
J Thorac Cardiovasc Surg. 1964 Jun;47:740-9.
5
Congenital unilateral absence of a pulmonary artery. The importance of flow in pulmonary hypertension.先天性单侧肺动脉缺如。血流在肺动脉高压中的重要性。
Am J Cardiol. 1962 Nov;10:706-32. doi: 10.1016/0002-9149(62)90248-5.
6
Congenital absence of a pulmonary artery. Report of a case, with special reference to the bronchial circulation and review of the literature.先天性肺动脉缺失。病例报告,并特别提及支气管循环及文献复习。
Am J Med. 1963 Feb;34:264-71. doi: 10.1016/0002-9343(63)90061-5.
7
Methods of altering circulatory dynamics to improve roentgen examination of the cardiovascular system; Chamberlain Lecture, 1961.改变循环动力学以改善心血管系统X线检查的方法;张伯伦讲座,1961年
Am J Roentgenol Radium Ther Nucl Med. 1963 Feb;89:233-53.
8
Development of the intrasegmental bronchial tree: the pattern of branching and development of cartilage at various stages of intra-uterine life.肺段内支气管树的发育:宫内生命各阶段的分支模式及软骨发育情况。
Thorax. 1961 Sep;16(3):207-18. doi: 10.1136/thx.16.3.207.
9
The number of alveoli in the terminal respiratory unit of man during late intrauterine life and childhood.人类子宫内晚期和儿童期终末呼吸单位中的肺泡数量。
Arch Dis Child. 1960 Dec;35(184):544-7. doi: 10.1136/adc.35.184.544.
10
Proximal interruption of a pulmonary arch (absence of one pulmonary artery); case report and a new embryologic interpretation.肺弓近端中断(一侧肺动脉缺如);病例报告及新的胚胎学解释
Dis Chest. 1958 Jul;34(1):73-86. doi: 10.1378/chest.34.1.73.