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非免疫性胎儿水肿与心包内畸胎瘤:病例报告及文献复习

Non-immunological hydrops fetalis and intrapericardial teratoma: case report and review.

作者信息

Perez-Aytes A, Sanchis N, Barbal A, Artés M J, Domene J, Chirivella M, Baamonde A

机构信息

Department of Pediatrics, Hospital Infantil La Fe, Valencia, Spain.

出版信息

Prenat Diagn. 1995 Sep;15(9):859-63. doi: 10.1002/pd.1970150912.

Abstract

A large intrapericardial teratoma was found at necropsy in a 38-week stillborn fetus, in which prenatal diagnosis of hydrops fetalis and an echogenic cardiac mass had been made. Clinical and pathological data are reported. In utero intrapericardial teratomata lead to different outcomes depending on whether fetal hydrops is associated. When generalized fetal hydrops is not present, the outcome is good, even in cases with large pericardial effusions. When generalized fetal hydrops occurs, it often results in a poor outcome. In our literature review, we have found eight perinatal deaths in nine similar cases reported.

摘要

在对一名38周死产胎儿进行尸检时发现一个巨大的心包内畸胎瘤,该胎儿产前诊断为胎儿水肿和心脏内有回声团块。报告了临床和病理数据。宫内心包内畸胎瘤根据是否伴有胎儿水肿会导致不同的结果。当不存在全身性胎儿水肿时,即使有心包大量积液,预后也良好。当发生全身性胎儿水肿时,往往导致不良预后。在我们的文献综述中,我们在报告的9例类似病例中发现了8例围产期死亡。

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