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小儿口咽神经鞘瘤1例罕见病例

A Rare Case of Pediatric Oropharyngeal Schwannoma.

作者信息

Rosi-Schumacher Mattie, Raghavan Maya, Pizzuto Michael

机构信息

Otolaryngology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, USA.

Pediatric Otolaryngology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, USA.

出版信息

Cureus. 2023 Oct 8;15(10):e46693. doi: 10.7759/cureus.46693. eCollection 2023 Oct.

Abstract

This is a case of a male child who presented with a progressively enlarging oropharyngeal mass, hyponasal voice, and symptoms of obstructive sleep apnea. Computed tomography imaging of the head and neck revealed a well-circumscribed low-density area of polypoid morphology arising from the left lateral pharyngeal wall, filling most of the posterior oropharynx and extending to a pedicle at the lateral nasopharynx. Histopathological evaluation following surgical excision revealed Antoni A tissue and S100 immunoreactivity. The presentation and diagnosis of benign schwannoma neoplasms are discussed.

摘要

这是一例男性患儿,表现为口咽肿物进行性增大、鼻音减退及阻塞性睡眠呼吸暂停症状。头颈部计算机断层扫描成像显示,左侧咽侧壁有一个边界清晰的息肉样低密度区,占据了大部分口咽后部,并延伸至鼻咽部外侧的蒂部。手术切除后的组织病理学评估显示为Antoni A组织及S100免疫反应性。本文讨论了良性神经鞘瘤的临床表现及诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d49/10628605/9ef3790de825/cureus-0015-00000046693-i01.jpg

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