Right-sided high origin of diaphragm associated with accessory lobe of liver, lobulated right atrial appendage, and ipsilateral phrenic nerve hamartoma: a case report.

John Kasznica, R. Praagh, Abraham T. Philip
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引用次数: 6

Abstract

A case of a rare condition of congenital right anterior high origin of the diaphragm in a stillborn fetus is reported. Associated findings at autopsy were a hornlike subdiaphragmatic intrathoracic accessory lobe of the liver and a lobulated right atrial appendage of the heart. At the superiormost aspect of the malpositioned right anterior diaphragmatic leaf a small phrenic nerve hamartoma was found. The phrenic nerve itself appeared small and not well developed. The phrenic nerve lesion may have been a concomitant or secondary hamartomatous change. Careful clinical and pathological search for concomitant anomalies in diaphragmatic lesions is emphasized.
右侧膈高起点伴肝副叶,分叶状右心房附件,同侧膈神经错构瘤1例。
一个罕见的情况下先天性右前高起点横膈膜在死产胎儿报告。尸检的相关发现是肝脏的角状膈下胸内副叶和心脏的分叶状右心房附件。在右膈前叶错位的最上方发现一个小膈神经错构瘤。膈神经本身显得小而不发达。膈神经病变可能伴随或继发错构瘤改变。仔细的临床和病理搜索伴随异常的膈病变强调。
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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