Clinicopathologic Features of Neuroblastoma-like Schwannoma: A Case Report of Unusual Morphologic Variant

Anatomia Pub Date : 2022-12-09 DOI:10.3390/anatomia1020022
S. Mortazavi, K. Kamyab Hesari, Atieh Khorsand, M. Ardalan
{"title":"Clinicopathologic Features of Neuroblastoma-like Schwannoma: A Case Report of Unusual Morphologic Variant","authors":"S. Mortazavi, K. Kamyab Hesari, Atieh Khorsand, M. Ardalan","doi":"10.3390/anatomia1020022","DOIUrl":null,"url":null,"abstract":"Neuroblastoma-like schwannoma is known as a rare unusual variant of schwannoma with difficulties of differential diagnosis with neuroblastoma, Ewing sarcoma/peripheral neuroectodermal tumor and other cutaneous small round cell tumors. Herein, we describe a neuroblastoma-like schwannoma that was presented as a painless lesion on the dorsal side of the left hand in a 39-year-old woman. Composed collagen fibers in the central core of rosettes and diffuse expression of S100 protein in the tumor cells found in the biopsy specimens confirmed the Schwann cell origin of the tumor.","PeriodicalId":7888,"journal":{"name":"Anatomia","volume":"374 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Anatomia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/anatomia1020022","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Neuroblastoma-like schwannoma is known as a rare unusual variant of schwannoma with difficulties of differential diagnosis with neuroblastoma, Ewing sarcoma/peripheral neuroectodermal tumor and other cutaneous small round cell tumors. Herein, we describe a neuroblastoma-like schwannoma that was presented as a painless lesion on the dorsal side of the left hand in a 39-year-old woman. Composed collagen fibers in the central core of rosettes and diffuse expression of S100 protein in the tumor cells found in the biopsy specimens confirmed the Schwann cell origin of the tumor.
神经母细胞瘤样神经鞘瘤的临床病理特征:异常形态变异1例报告
神经母细胞瘤样神经鞘瘤是一种罕见的神经鞘瘤变体,与神经母细胞瘤、尤因肉瘤/周围神经外胚层肿瘤和其他皮肤小圆细胞瘤鉴别诊断困难。在此,我们描述了一个39岁女性的神经母细胞瘤样神经鞘瘤,表现为左手背侧的无痛病变。玫瑰花中心核心的胶原纤维组成和活检标本中肿瘤细胞中S100蛋白的弥漫性表达证实了肿瘤的雪旺细胞起源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信