Hypertrophic cardiomyopathy associated with an anomalous origin of right coronary artery Case report and review of the literature

被引：5
|
作者：
Efthimiadis, G. K. [1 ]
Theofilogiannakos, E. K. [1 ]
Gossios, T. D. [1 ]
Paraskevaidis, S. [1 ]
Vassilikos, V. P. [1 ]
Styliadis, I. H. [1 ]
机构：
[1] Aristotle Univ Thessaloniki, AHEPA Hosp, Dept Cardiol 1, Cardiomyopathies Ctr, Thessaloniki 54250, Greece
来源：
HERZ | 2013年 / 38卷 / 04期
关键词：
Hypertrophic cardiomyopathy; Congenital coronary anomaly; Sudden cardiac death; SUDDEN-DEATH; OBSTRUCTIVE CARDIOMYOPATHY; RIGHT SINUS; PATIENT; VALSALVA; CHILDREN; VARIANT; OSTIA;
D O I：
10.1007/s00059-012-3713-y
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
We present a case of patient with hypertrophic cardiomyopathy and an anomalous right coronary artery with left main artery origin and an interarterial course. The coexistence of these two different entities is extremely rare but of major clinical significance because both are associated with an increased risk of sudden cardiac death. In addition, a review of the literature comprising 14 other cases with this combination is provided.
引用
收藏
页码：427 / 430
页数：4
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