Giant Morgagni hernia and aorto-pulmonary collaterals in a Loeys-Dietz patient undergoing surgery for aortic root aneurysm and mitral valve prolapse.

0 CARDIAC & CARDIOVASCULAR SYSTEMS
Federica Lo Presti, Giuseppe Palmiero, Giuseppe Limongelli, Alessandro Della Corte
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Abstract

The case of a Loeys-Dietz syndrome patient undergoing mitral valve repair and composite aortic root and valve replacement is here described: preoperative CT scan unravelled a previously misdiagnosed Morgagni hernia (anterior diaphragmatic), containing omentum only, compressing the right ventricle. Intraoperatively, an abnormal oxygenated blood backflow into the left ventricle was observed, postoperatively found to be caused by major aorto-pulmonary collateral arteries. This is the 1st case of Morgagni hernia and systemic-pulmonary shunt ever reported associated with Loeys-Dietz syndrome. These congenital features may be important in both phenotyping and surgical management.

一名因主动脉根部动脉瘤和二尖瓣脱垂而接受手术的 Loeys-Dietz 患者的巨大莫尔加尼疝和主动脉-肺动脉袢。
这里描述的是一名接受二尖瓣修复术和主动脉根部及瓣膜复合置换术的 Loeys-Dietz 综合征患者的病例:术前 CT 扫描发现了之前误诊的莫加尼疝(膈前),仅包含网膜,压迫右心室。术中观察到异常的含氧血液倒流到左心室,术后发现是由主要的主动脉-肺侧动脉引起的。这是首例与 Loeys-Dietz 综合征相关的莫加尼疝和全身-肺分流病例。这些先天性特征可能对表型和手术治疗都很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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