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枕部头皮“先天性”丛状神经纤维瘤。病例报告。

"Congenital" plexiform neurofibroma of the occipital scalp. Case report.

作者信息

Ohaegbulam S C

出版信息

J Neurosurg. 1977 Feb;46(2):245-7. doi: 10.3171/jns.1977.46.2.0245.

DOI:10.3171/jns.1977.46.2.0245
PMID:833642
Abstract

An occipital scalp tumor first noted in a Nigerian girl during the first month of her life gradually increased in size and 13 years later measured 10 X 16 X 17 cm. A skull film revealed a 2 X 4-cm skull defect underneath the tumor over the lambdoid suture. Complete excision of the tumor was achieve although it was adherent to the dura of the transverse sinus. It was histologically confirmed to be plexiform neurofibroma. There were no other signs of van Recklinghausen's neurofibromatosis.

摘要

一名尼日利亚女孩在出生后的第一个月首次被发现枕部头皮有肿瘤,肿瘤大小逐渐增大,13年后尺寸为10×16×17厘米。颅骨X光片显示,在肿瘤下方的人字缝处有一个2×4厘米的颅骨缺损。尽管肿瘤与横窦硬脑膜粘连,但仍成功将其完全切除。组织学检查证实为丛状神经纤维瘤。没有其他冯·雷克林豪森神经纤维瘤病的迹象。

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Craniomaxillofac Trauma Reconstr. 2018 Dec;11(4):324-330. doi: 10.1055/s-0037-1608699. Epub 2017 Dec 4.
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Congenital extra calvarial plexiform neurofibroma in occipito-cervical region with Occipital bone defect with neurofibromatosis type 1 and segmental neurofibromatosis: Case report and review of literature.
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