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沙漏状颅面畸胎瘤(作者译)

[Hour-glass craniofacial teratoma (author's transl)].

作者信息

Freidel M, Dodat H, Deruty R

出版信息

Rev Stomatol Chir Maxillofac. 1979;80(5):305-10.

PMID:291116
Abstract

A male infant was born with a voluminous left jugal swelling identified by biopsy on the 8th day as a mature benign teratoma. Further investigations were conducted because of mild exophthalmia, including an electro-encephalogram and craniofacial computer tomography. An enormous frontotemporal intracranial extension of the tumor was discovered on the same side. The tumor was completely excised at the age of 1 month by a two-stage operation : neurosurgical followed by maxillofacial eight days later. The postoperative course was uneventful. There was no relapse after one year but because of the consequences of intracranial excision the prognosis was very poor. The authors discuss this case and review those in the published literature in order to describe the diagnosis, treatment, and prognosis of this extremely rare craniofacial teratoma of the newborn.

摘要

一名男婴出生时左颧部有巨大肿物,第8天活检确诊为成熟性良性畸胎瘤。因轻度眼球突出进一步检查,包括脑电图和颅面计算机断层扫描。发现肿瘤同侧有巨大的额颞部颅内扩展。1个月时通过两阶段手术完全切除肿瘤:先神经外科手术,8天后行颌面手术。术后过程顺利。1年后无复发,但由于颅内切除的后果,预后很差。作者讨论了该病例并回顾了已发表文献中的病例,以描述这种极其罕见的新生儿颅面畸胎瘤的诊断、治疗和预后。

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