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儿童下颌骨骨内神经鞘瘤:1例罕见病例报告

Mandibular intraosseous schwannoma in a child: Report of a rare case.

作者信息

Kargahi Neda, Razavi Seyed Mahammad, Hasheminia Darioush, Keshani Forouz, Safaei Mehran, Hashemzadeh Zahra

机构信息

Torabinejad Dental Research Center and Department of Oral and Maxillofacial Pathology, School of Dentistry, Isfahan University of Medical Science, Isfahan, Iran.

出版信息

Dent Res J (Isfahan). 2012 Dec;9(Suppl 1):S119-22.

Abstract

Intraosseous schwannomas is a very rare neoplasm, and less than 50 cases have been reported in the medical literature. In this article, the clinical, radiographic and histopathologic appearances of a rare case of intraosseous schwannomas are presented. The importance of this case is that other benign central lesions such as odontogenic tumors and cysts might be included in differential diagnosis. This case was recognized in a 9-year-old child, which is a very rare occurrence. The diagnosis was confirmed by immunohistochemical staining with S100 protein.

摘要

骨内施万细胞瘤是一种非常罕见的肿瘤,医学文献中报道的病例不足50例。本文介绍了一例罕见的骨内施万细胞瘤的临床、影像学和组织病理学表现。该病例的重要性在于,在鉴别诊断中可能需要考虑其他良性中心性病变,如牙源性肿瘤和囊肿。该病例发生在一名9岁儿童身上,极为罕见。通过S100蛋白免疫组化染色确诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42bf/3692190/cca70b4b5f15/DRJ-9-119-g001.jpg

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