Massively Hypertrophied Right-Sided Heart with Hypoplastic Left-Sided Heart in a Neonate (A Rare Type of Hypertrophic Cardiomyopathy)

被引:0
|
作者
Roberts, William C. [1 ,2 ,3 ,4 ]
Chinta, Sindhu [1 ]
Guileyardo, Joseph M. [3 ]
机构
[1] Baylor Univ, Baylor Scott & White Heart & Vasc Inst, Baylor Scott & White Hlth, Med Ctr, Dallas, TX USA
[2] Baylor Univ, Dept Internal Med, Baylor Scott & White Hlth, Med Ctr, Dallas, TX USA
[3] Baylor Univ, Dept Pathol, Baylor Scott & White Hlth, Med Ctr, Dallas, TX USA
[4] Baylor Scott & White Heart & Vasc Inst, 621 N Hall St,Suite H-030, Dallas, TX 75226 USA
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2023年 / 190卷
关键词
Hypertrophic cardiomyopathy; atrial septal defect; patent ductus arteriosus; hypo; plastic left-sided heart; RIGHT-VENTRICULAR HYPERTROPHY; TRANSIENT;
D O I
10.1016/j.amjcard.2022.11.024
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Described herein is a newborn boy with likely right-sided hypertrophic cardiomyopathy (HC), who survived for 18 hours after birth. At necropsy, he had a severely thickened right ventricular free wall, ventricular septum, right atrial wall and a hypoplastic left-sided heart. There was a large fossa ovale type atrial septal defect and also a patent ductus arteriosus. During peak systole, the right ventricular outflow tract was obstructed, and its contents were pushed into the thick-walled right atrium, then rapidly into the thin-walled left atrium via a large fossa ovale atrial septal defect. The contents were then pushed into the thin-walled left ventricle and finally into the small ascending aorta and into the lungs via a large patent ductus arteriosus. We were unable to find a similar published case. (c) 2022 Elsevier Inc. All rights reserved. (Am J Cardiol 2023;190:126-130)
引用
收藏
页码:126 / 130
页数:5
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