Noncompaction cardiomyopathy in Hirschsprung's disease: a case report

被引：1

作者：

Visona, Silvia D. ^{[1
]}

Thiene, Gaetano ^{[2
]}

Mannarino, Savina ^{[3
]}

Corana, Giulia ^{[3
]}

Osculati, Antonio ^{[1
]}

Angelini, Annalisa ^{[2
]}

Rizzo, Stefania ^{[2
]}

机构：

[1] Univ Pavia, Dept Publ Hlth Expt & Forens Med, Unit Legal Med & Forens Sci Antonio Fornari, Pavia, Italy

[2] Univ Padua, Dept Cardiac Thorac & Vasc Sci, Via Gabelli 61, I-35121 Padua, Italy

[3] Univ Pavia, Fdn IRCCS Policlin San Matteo, Dept Pediat, Pavia, Italy

来源：

CARDIOVASCULAR PATHOLOGY | 2017年 / 27卷

关键词：

Noncompaction cardiomyopathy; Hirschsprung's disease; Neural crest; VENTRICULAR NON-COMPACTION; CLASSIFICATION; MYOCARDIUM; CARDIOLOGY; STATEMENT; FAILURE;

D O I：

10.1016/j.carpath.2016.12.005

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Noncompaction cardiomyopathy is a rare disorder, often associated with cardiac and noncardiac malformations. Hirschsprung's disease, a well-known aganglionosis, is associated with congenital heart diseases and has been reported to be due to impairment migration and differentiation of neural crest cells. Here, we present an 8-month-old male infant who died for cardiogenic shock after surgical resection of the involved bowel segment. The child was affected by both noncompaction cardiomyopathy and Hirschsprung's disease, two entities which can share a common neural crest-derived etiology. (C) 2017 Elsevier Inc. All rights reserved.

引用

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页码：51 / 53

页数：3

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