Epithelioid schwannoma in the buccal region: A case report and review of literature

IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Takashi Baba , Hiroshi Baba , Yu Yamaguma , Takehito Fukui , Takeshi Kaneuji , Yoshihiro Yamashita
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Abstract

Schwannomas are common, benign peripheral nerve sheath tumors that arise from Schwann cells. Several rare morphological variants include ancient, cellular, plexiform, epithelioid, and microcystic/reticular. The epithelioid variant of schwannoma is scarce, with only a few relevant cases reported in the oral and maxillofacial regions. Herein, we report a case of epithelioid schwannoma in the buccal region. A 61-year-old woman was referred to our department from a medical clinic because of a slow-growing nodule in the buccal region, noticed 3 years before presentation. Clinical examination revealed a nodular mass measuring 20 × 20 mm. Computed tomography (CT) and magnetic resonance imaging (MRI) showed an oval lesion with a clear border on the left cheek. The outer margin of the mass exhibited opacities that appeared as multiple microcalcifications. MRI revealed a well-defined mass similar in size to that observed on CT, with low signal intensity on T1-weighted images and mildly high signal intensity on T2-weighted images. The clinical differential diagnosis includes benign tumors such as pleomorphic adenoma. The tumor was surgically excised under general anesthesia. Histopathological examination revealed multilobulated epithelioid cells arranged in nests. The tumor cells showed eosinophilic cytoplasm and uniformly round nuclei. The tumor was diagnosed as an epithelioid schwannoma. Postoperative follow-up was uneventful, and no evidence of recurrence was observed 2 years postoperatively.
颊部上皮样神经鞘瘤1例报告及文献复习
神经鞘瘤是一种常见的良性周围神经鞘肿瘤,起源于雪旺细胞。几种罕见的形态变异包括古老的、细胞的、丛状的、上皮样的和微囊/网状的。神经鞘瘤的上皮样变异是罕见的,只有少数相关的病例报道在口腔和颌面区域。在此,我们报告一例颊部上皮样神经鞘瘤。一名61岁女性因颊部长有一生长缓慢的结节,于就诊前3年就诊于我科。临床检查发现结节状肿块,尺寸为20 × 20 mm。计算机断层扫描(CT)和磁共振成像(MRI)显示左脸颊椭圆形病变,边界清晰。肿块外缘表现为多发微钙化的混浊。MRI示清晰的肿块,大小与CT相似,t1加权像呈低信号,t2加权像呈轻度高信号。临床鉴别诊断包括良性肿瘤,如多形性腺瘤。肿瘤在全身麻醉下手术切除。组织病理学检查显示巢内排列有多分叶上皮样细胞。肿瘤细胞胞浆嗜酸性,细胞核均匀圆形。肿瘤被诊断为上皮样神经鞘瘤。术后随访顺利,术后2年无复发迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
129
审稿时长
83 days
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