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模仿孤立性颊部肿物的咬肌内施万瘤:病例报告及文献复习

Intramasseteric Schwanoma mimicking an isolated cheek mass: Case report and review of literature.

作者信息

El Khatib Nazir, Nehme Antoine, Nasser Selim, Moukarzel Nabil, Abtar Houssam Khodor

机构信息

Sacre-Coeur Hospital, Lebanese University, ENT Department, Beirut, Lebanon.

Sacre-Coeur Hospital, Lebanese University, Department of Pathology, Beirut, Lebanon.

出版信息

Int J Surg Case Rep. 2018;46:24-27. doi: 10.1016/j.ijscr.2018.03.042. Epub 2018 Apr 7.

DOI:10.1016/j.ijscr.2018.03.042
PMID:29656234
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6000762/
Abstract

INTRODUCTION

Schwannoma is a benign well circumscribed tumor of the nerve sheath and it is mostly localized in the head and neck. Intramasseteric schwannoma represents a very rare entity and a few cases have been described in the literature.

PRESENTATION OF CASE

We present a case of an isolated, asymptomatic and slowly progressive right cheek tumor in a middle aged man. Although multiple investigations, including neck scanner and fine needle aspiration, were done, the diagnosis was obscure and difficult before definite surgical resection. Surgery showed an isolated and well-defined tumor inside the masseter muscle which was completely resected. Histopathologic finding confirmed the diagnosis of schwannoma with the characteristic Antoni A and Antoni B cells.

DISCUSSION

Among benign tumors of the peripheral nerves, schwannoma is a specific type that originates from Schwann cells. It is typically slowly growing, neoplasm that is displacing neural structures without direct invasion. History, physical examination, fine needle aspiration, and magnetic resonance imaging are used as diagnostic modalities, however definitive diagnosis and identification of the affected nerve are often difficult up to the time of surgery.

CONCLUSION

Herby we describe a very rare localization of schwannoma arising from masseter muscle in a 30 year old man who presents with painless neck mass. This rare entity should be considered in the differential diagnosis in any patient presented with cheek mass.

摘要

引言

施万细胞瘤是一种边界清晰的神经鞘良性肿瘤,多位于头颈部。咬肌内施万细胞瘤是一种非常罕见的疾病,文献中仅有少数病例报道。

病例介绍

我们报告一例中年男性患者,其右侧脸颊出现一个孤立、无症状且进展缓慢的肿瘤。尽管进行了包括颈部扫描和细针穿刺在内的多项检查,但在明确手术切除前,诊断仍不明确且困难。手术显示咬肌内有一个孤立且边界清晰的肿瘤,已被完全切除。组织病理学检查结果证实为施万细胞瘤,可见特征性的Antoni A和Antoni B细胞。

讨论

在周围神经良性肿瘤中,施万细胞瘤是一种起源于施万细胞的特殊类型。它通常生长缓慢,是一种推移神经结构而不直接侵犯的肿瘤。病史、体格检查、细针穿刺和磁共振成像被用作诊断方法,然而,直到手术时,明确诊断和确定受影响的神经往往仍很困难。

结论

在此,我们描述了一例罕见的施万细胞瘤,发生于一名30岁男性的咬肌,表现为无痛性颈部肿块。对于任何出现脸颊肿块的患者,在鉴别诊断时都应考虑到这种罕见疾病。

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