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横纹肌瘤与左心发育不全综合征——一种极为罕见组合的病例报告

Rhabdomyoma and Hypoplastic Left Heart Syndrome - Case Report of a Very Rare Combination.

作者信息

Waggass Rahaf, Bin Yahib Hanan S, Bin Seddeq Hosam H, Shawli Aiman

机构信息

Cardiac Sciences, Ministry of National Guard - Health Affairs, Jeddah, SAU.

Medicine, King Saud bin Abdulaziz University for Health Sciences, Jeddah, SAU.

出版信息

Cureus. 2021 Nov 25;13(11):e19900. doi: 10.7759/cureus.19900. eCollection 2021 Nov.

DOI:10.7759/cureus.19900
PMID:34976510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8712222/
Abstract

The most benign cardiac tumor in the pediatric population is cardiac rhabdomyoma. They are known to be associated with tuberous sclerosis complex. Here we report a case with multiple cardiac rhabdomyomas and another rare anomaly of the heart known as hypoplastic left heart syndrome. The fetus was antenatally diagnosed with echocardiography which showed both rhabdomyoma and hypoplastic left heart. The patient was started on prostaglandin immediately after birth. He was confirmed postnatally to have inoperable congenital hypoplastic left heart syndrome. On the third day, the baby started to have progressive bradycardia and then died.

摘要

小儿人群中最良性的心脏肿瘤是心脏横纹肌瘤。已知它们与结节性硬化症复合体相关。在此，我们报告一例患有多发性心脏横纹肌瘤以及另一种罕见心脏异常即左心发育不全综合征的病例。该胎儿在产前通过超声心动图被诊断出患有横纹肌瘤和左心发育不全。患儿出生后立即开始使用前列腺素。出生后确诊为无法手术的先天性左心发育不全综合征。第三天，婴儿开始出现进行性心动过缓，随后死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fad6/8712222/db7efd4481ce/cureus-0013-00000019900-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fad6/8712222/6890e79daf9c/cureus-0013-00000019900-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fad6/8712222/db7efd4481ce/cureus-0013-00000019900-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fad6/8712222/6890e79daf9c/cureus-0013-00000019900-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fad6/8712222/db7efd4481ce/cureus-0013-00000019900-i02.jpg

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Unusual Outcome of a Right Ventricular Rhabdomyoma in an Infant.一名婴儿右心室横纹肌瘤的罕见结局
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