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家族性心肌病、性腺功能减退和胶原瘤。

Familial cardiomyopathy, hypogonadism, and collagenoma.

作者信息

Sacks H N, Crawley I S, Ward J A, Fine R M

出版信息

Ann Intern Med. 1980 Dec;93(6):813-7. doi: 10.7326/0003-4819-93-6-813.

Abstract

A patient with tricuspid regurgitation by clinical evaluation, cardiac catheterization, and angiography was found at autopsy to have a cardiomyopathy involving both ventricles but with predominant involvement of the right ventricle. He also had primary testicular failure and a distinctive type of collagenoma. The patient's two brothers were examined and found to have similar collagenomas and testicular failure. Evidence for a mild to moderate degree of cardiomyopathy was also apparent by findings on physical examination, chest roentgenogram, electrocardiogram, and echocardiogram. The father was known to have had a similar skin lesion and congestive heart failure. The aspects of the clinical presentation of this patient and the findings in the two brothers are discussed. A common genetic link in this familial syndrome is not elucidated.

摘要

一名经临床评估、心导管检查和血管造影诊断为三尖瓣反流的患者,尸检发现患有累及双心室的心肌病,但以右心室受累为主。他还患有原发性睾丸功能衰竭和一种特殊类型的胶原瘤。对患者的两个兄弟进行检查,发现他们也有类似的胶原瘤和睾丸功能衰竭。通过体格检查、胸部X线、心电图和超声心动图检查结果,也明显显示出轻度至中度心肌病的证据。已知患者的父亲有类似的皮肤病变和充血性心力衰竭。本文讨论了该患者的临床表现及两个兄弟的检查结果。尚未阐明这种家族性综合征的共同遗传联系。

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