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成人左房三房心表现为二尖瓣狭窄。

Cor triatriatum sinister presenting in the adult as mitral stenosis.

作者信息

Slight R D, Nzewi O C, Sivaprakasam R, Mankad P S

机构信息

Department of Cardiothoracic Surgery, The Royal Infirmary of Edinburgh, Little France, Edinburgh, UK.

出版信息

Heart. 2003 Oct;89(10):e26. doi: 10.1136/heart.89.10.e26.

DOI:10.1136/heart.89.10.e26
PMID:12975448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1767893/
Abstract

Cor triatriatum sinister is a rare congenital defect in which the left atrium is divided by a fibromuscular membrane into two distinct chambers. Classically, patients present in infancy although in some cases they remain asymptomatic until adulthood. The clinical features on presentation can mimic those of mitral stenosis due to the obstructive properties of the membrane. Cor triatriatum sinister presented in this case in an adult as mitral stenosis. Factors that may be relevant in determining late presentation are also discussed.

摘要

左房三房心是一种罕见的先天性缺陷,其中左心房被纤维肌性隔膜分隔为两个不同的腔室。典型情况下,患者在婴儿期发病,不过在某些病例中,他们直到成年都无症状。由于隔膜的阻塞特性,发病时的临床特征可类似于二尖瓣狭窄。该病例中的左房三房心在一名成年人中表现为二尖瓣狭窄。文中还讨论了可能与延迟发病相关的因素。

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本文引用的文献

1
Diagnosis and surgical correction of cor triatriatum in an adult: combined use of transesophageal echocardiography and catheterization.成人三房心的诊断与手术矫正:经食管超声心动图与心导管检查的联合应用
Catheter Cardiovasc Interv. 2000 Sep;51(1):83-6. doi: 10.1002/1522-726x(200009)51:1<83::aid-ccd19>3.0.co;2-7.
2
Cor triatriatum: diagnosis, operative approach, and late results.三房心:诊断、手术方法及远期结果。
Mayo Clin Proc. 1993 Sep;68(9):854-9. doi: 10.1016/s0025-6196(12)60693-4.
3
Myxomatous mitral valve degeneration complicating asymptomatic cor triatriatum.
Clin Cardiol. 1989 Jan;12(1):48-50. doi: 10.1002/clc.4960120110.
4
Initial presentation of cor triatriatum in a 55-year-old woman.一名55岁女性三房心的初次表现。
Am Heart J. 1992 Sep;124(3):788-91. doi: 10.1016/0002-8703(92)90295-7.