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胎儿心包畸胎瘤的产前切除术。

Prenatal resection of a fetal pericardial teratoma.

作者信息

Sydorak Roman M, Kelly Thomas, Feldstein Vickie A, Sandberg Per L, Silverman Norman H, Harrison Michael R, Albanese Craig T

机构信息

The Fetal Treatment Center, University of California, San Francisco, Calif. 94143-0570, USA.

出版信息

Fetal Diagn Ther. 2002 Sep-Oct;17(5):281-5. doi: 10.1159/000063180.

Abstract

OBJECTIVE

Pericardial teratomas are rare congenital tumors which invade the developing mediastinum, compressing the venous return to the heart, leading to hydrops. Tumors, with large cystic components, have been treated previously with in utero pericardiocentesis with some success. We present the first reported case of in utero open resection of a fetal pericardial teratoma.

METHODS

A 31-year-old G1P0 woman was found to have a fetus with a pericardial teratoma. Hydrops developed at 24 weeks' gestation. After counseling, open fetal resection was performed via a fetal median sternotomy.

RESULTS

Although the tumor was successfully removed, the hydrops did not resolve. In addition, over the course of 3 weeks, the mother developed maternal mirror syndrome which prompted an emergent cesarean section. Neonatal death ensued shortly after birth.

CONCLUSIONS

The fetus with a pericardial teratoma complicated by hydrops is compromised. Treatment options include early delivery, aspiration of the pericardial effusion, and in utero operative resection.

摘要

目的

心包畸胎瘤是一种罕见的先天性肿瘤,可侵犯正在发育的纵隔,压迫心脏的静脉回流,导致水肿。对于含有大囊性成分的肿瘤,以往曾采用宫内心包穿刺术进行治疗,取得了一定的成功。我们报告首例胎儿心包畸胎瘤宫内开放性切除术。

方法

一名31岁的初产妇被发现其胎儿患有心包畸胎瘤。妊娠24周时出现水肿。经过咨询后,通过胎儿正中胸骨切开术进行了开放性胎儿切除术。

结果

虽然肿瘤被成功切除,但水肿并未消退。此外,在3周的时间里,母亲出现了母体镜像综合征,促使紧急剖宫产。新生儿出生后不久死亡。

结论

患有心包畸胎瘤并伴有水肿的胎儿情况危急。治疗选择包括早产、心包积液抽吸和宫内手术切除。

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