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双心室心肌致密化不全伴重度肺动脉瓣狭窄及卵圆孔未闭

Biventricular Noncompaction Cardiomyopathy Accompanied by Severe Pulmonary Valvular Stenosis and Patent Foramen Ovale.

作者信息

Karauzum Kurtulus, Karauzum Irem Yilmaz, Sahin Tayfun, Kilic Teoman

机构信息

Department of Cardiology, Medical Faculty, Kocaeli University, Kocaeli, Turkey.

出版信息

J Cardiovasc Echogr. 2018 Apr-Jun;28(2):138-140. doi: 10.4103/jcecho.jcecho_50_17.

Abstract

Myocardial non-compaction (NC) is a rare genetic cardiomyopathy commonly believed to develop an intrauterine arrest of endomyocardial morphogenesis. NC is characterized by markedly hypertrabeculations in left ventricle or both ventricles with deep intertrabecular recesses. NC is usually seen isolated, but sometimes other congenital heart abnormalities may accompany to the myocardial NC. In this article we have presented an adult patient with biventricular myocardial NC cardiomyopathy accompanied by severe valvular pulmonary stenosis and patent foramen ovale.

摘要

心肌致密化不全(NC)是一种罕见的遗传性心肌病,通常认为是由于宫内心内膜形态发生停滞所致。NC的特征是左心室或双心室有明显的粗大肌小梁和深陷的小梁间隐窝。NC通常单独出现,但有时其他先天性心脏异常可能与心肌NC并存。在本文中,我们报告了一例成年患者,患有双心室心肌致密化不全性心肌病,伴有严重的瓣膜性肺动脉狭窄和卵圆孔未闭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/5989548/1c93edc25a25/JCE-28-138-g001.jpg

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