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一种伴有预激综合征的不寻常类型的局限性肥厚型心肌病并出现肺水肿。

An Unusual Type of Localized Hypertrophic Cardiomyopathy With Wolf Parkinson White Syndrome Presenting With Pulmonary Edema.

作者信息

Vatan Mehmet Bulent, Gunduz Huseyin, Gurel Safiye, Kocayigit Ibrahim, Vural Ahmet, Demirtas Saadet, Cakar Mehmet Akif, Gunduz Yasemin

机构信息

Sakarya University, Medical faculty, Deparmet of Cardiology, Sakarya, Turkey.

Abant izzet Baysal University Bolu Medical faculty, Deparmet of Radiology, Bolu, Turkey.

出版信息

Cardiol Res. 2012 Jun;3(3):133-136. doi: 10.4021/cr138w. Epub 2012 May 20.

DOI:10.4021/cr138w
PMID:28352409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5358242/
Abstract

Hypertrophic cardiomyopathy (HCM) is an autosomal dominant heart disease that is the most common genetic cardiac disorder. The disease is characterized by excessive thickening of the left ventricular myocardium. The anterior portion of the interventricular ventricular septum is often involved. Asymmetric hypertrophy of apical site, left ventricular free wall, and right ventricle are less common in hypertrophic cardiomyopathy that occur in 1% cases. We report a case of a patient with an unusual type of hypertrophic cardiomyopathy and Wolf Parkinson White (WPW) presenting with pulmonary edema.

摘要

肥厚型心肌病（HCM）是一种常染色体显性遗传性心脏病，是最常见的遗传性心脏疾病。该病的特征是左心室心肌过度增厚。室间隔前部常受累。心尖部位、左心室游离壁和右心室的不对称肥厚在肥厚型心肌病中较少见，发生率为1%。我们报告一例患有罕见类型肥厚型心肌病和预激综合征（WPW）并伴有肺水肿的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/5358242/afb97fbc952e/cr-03-133-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/5358242/1727c3ba3918/cr-03-133-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/5358242/9370d09d3a33/cr-03-133-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/5358242/e04fbd5e3c99/cr-03-133-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/5358242/afb97fbc952e/cr-03-133-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/5358242/1727c3ba3918/cr-03-133-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/5358242/9370d09d3a33/cr-03-133-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/5358242/e04fbd5e3c99/cr-03-133-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/5358242/afb97fbc952e/cr-03-133-g004.jpg

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本文引用的文献

1
Mutation of the MYH7 gene in a child with hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome.
J Appl Genet. 2007;48(2):185-8. doi: 10.1007/BF03194677.
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Hypertrophic cardiomyopathy with massive midventricular hypertrophy, midventricular obstruction and an akinetic apical chamber.肥厚型心肌病伴巨大心室中部肥厚、心室中部梗阻及心尖部室腔运动不能。
Anadolu Kardiyol Derg. 2006 Sep;6(3):279-82.
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Glycogen storage diseases presenting as hypertrophic cardiomyopathy.表现为肥厚型心肌病的糖原贮积病。
N Engl J Med. 2005 Jan 27;352(4):362-72. doi: 10.1056/NEJMoa033349.
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Delayed contrast enhancement of MRI in hypertrophic cardiomyopathy.肥厚型心肌病的MRI延迟强化
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Hypertrophic cardiomyopathy: a systematic review.肥厚型心肌病：一项系统综述。
JAMA. 2002 Mar 13;287(10):1308-20. doi: 10.1001/jama.287.10.1308.
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The molecular genetic basis for hypertrophic cardiomyopathy.肥厚型心肌病的分子遗传学基础。
J Mol Cell Cardiol. 2001 Apr;33(4):655-70. doi: 10.1006/jmcc.2001.1340.
7
Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome progressing to ventricular dilation.伴有预激综合征的家族性肥厚型心肌病进展为心室扩张。
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Phenotypic spectrum and patterns of left ventricular hypertrophy in hypertrophic cardiomyopathy: morphologic observations and significance as assessed by two-dimensional echocardiography in 600 patients.肥厚型心肌病患者左心室肥厚的表型谱及模式：600例患者二维超声心动图评估的形态学观察及意义
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9
Hypertrophic cardiomyopathy characterized by marked hypertrophy of the posterior left ventricular free wall: significance and clinical implications.以左心室后壁显著肥厚为特征的肥厚型心肌病：意义及临床影响
J Am Coll Cardiol. 1991 Aug;18(2):421-8. doi: 10.1016/0735-1097(91)90595-z.