Suppr超能文献

头皮孤立性巨大弥漫性神经纤维瘤伴颅骨缺损。

Solitary giant diffuse neurofibroma of the scalp with calvarial defect.

作者信息

Kumar Sanjeev, Chaurasia Pramod, Singh Daljit, Batra Vineeta V, Aher Rajendra

机构信息

Department of Neurosurgery, G.B.Pant Hospital, New Delhi, India.

Department of Pathology, G.B.Pant Hospital, New Delhi, India.

出版信息

Asian J Neurosurg. 2017 Apr-Jun;12(2):263-265. doi: 10.4103/1793-5482.144199.

Abstract

Neurofibromas of the scalp can have protean presentations. Most of the swellings are small, solitary and are easily diagnosed clinically. Diffuse swellings on the other hand are rare and are commonly seen in adults. The skull defects with these swellings are also rarely reported in the absence of neurofibromatosis. There is only one report of child having diffuse neurofibroma with skull defect. We report a second case in literature in a child with progressive, painful, diffuse neurofibroma along with calvarial defect.

摘要

头皮神经纤维瘤可有多种表现形式。大多数肿物较小,为单发,临床上易于诊断。另一方面,弥漫性肿物较为罕见,常见于成年人。在无神经纤维瘤病的情况下,伴有这些肿物的颅骨缺损也鲜有报道。仅有一篇关于儿童患有伴有颅骨缺损的弥漫性神经纤维瘤的报道。我们报告了文献中的第二例病例,是一名患有进行性、疼痛性弥漫性神经纤维瘤及颅骨缺损的儿童。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d9/5409383/efce370dcd3e/AJNS-12-263-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验