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硬腭巨大畸胎瘤:一例报告

A large teratoma of the hard palate: a case report.

作者信息

Benson R E, Fabbroni G, Russell J L

机构信息

Oral and Maxillofacial Surgery, Leeds General Infirmary, United Kingdom.

出版信息

Br J Oral Maxillofac Surg. 2009 Jan;47(1):46-9. doi: 10.1016/j.bjoms.2007.12.015. Epub 2008 Jul 3.

Abstract

Congenital teratoma is a rare malformation, and few papers have been published about it. We present a large teratoma that arose from the hard palate in a neonate. The obstructive mass caused maternal polyhydramnios and was identified prenatally by ultrasonography. The mother went into labour at 35 week's gestation at home. The child was in respiratory distress as a result of airway obstruction, and a tracheostomy was done when she was 4hours old. She also had major cardiac abnormalities. The palatal mass was removed successfully at 4 weeks of age. The typical components of a teratoma were identified including immature neural glial tissue.

摘要

先天性畸胎瘤是一种罕见的畸形,关于它的论文发表较少。我们报告一例源于新生儿硬腭的巨大畸胎瘤。阻塞性肿块导致母亲羊水过多,产前通过超声检查得以确诊。母亲在妊娠35周时在家中分娩。由于气道阻塞,患儿出生后即出现呼吸窘迫,出生4小时后行气管切开术。她还伴有严重的心脏异常。患儿在4周龄时成功切除腭部肿块。病理检查发现畸胎瘤的典型成分,包括未成熟的神经胶质组织。

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