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发生于下颌下腺的微囊型/网状神经鞘瘤:一种罕见的良性病变,可酷似更常见的涎腺癌。

Microcystic/Reticular Schwannoma Arising in the Submandibular Gland: A Rare Benign Entity that Mimics More Common Salivary Gland Carcinomas.

作者信息

Lau Ryan P, Melamed Jonathan, Yee-Chang Melissa, Marcus Sonya, Givi Babak, Zamuco Ronaldo

机构信息

Department of Pathology, New York University School of Medicine, 462 1st Avenue, Office 4W35, New York, NY, 10016, USA.

Department of Otolaryngology - Head and Neck Surgery, New York University School of Medicine, 462 First Avenue, Suite 5SE5, New York, NY, 10016, USA.

出版信息

Head Neck Pathol. 2016 Sep;10(3):374-8. doi: 10.1007/s12105-015-0674-5. Epub 2015 Nov 30.

Abstract

Microcystic/reticular schwannoma is a recently described variant of schwannoma with a predilection for the gastrointestinal tract, rarely involving the head/neck region. This is the first reported case involving the submandibular gland. We present a case in a 34 year old man with 4.5 cm submandibular mass. Fine needle aspiration suggested a spindle cell lesion. Frozen section evaluation raised the possibility of mucoepidermoid carcinoma. Resection showed a well circumscribed mass with a mucoid appearance. Histologic findings include a lobular architecture with fibrous septa, a lympho-plasmacytic infiltrate, and scattered lymphoid aggregates at the periphery. There are two distinct histologic patterns with solid areas of spindle cells and areas of spindle/ovoid cells with a microcystic pattern in a myxoid background. The tumor has a pushing border, with extension into adipose and adjacent parenchyma, without cytologic atypia or necrosis. Immunohistochemical stains are positive for S-100 and CD34, and negative for calponin, mammoglobin, ALK1, p63, ER, GFAP, SMA, desmin, cytokeratin 7, cytokeratin AE1/AE3, and C-Kit. Mucicarmine stain is negative. Recognition of this benign unusual variant of schwannoma is paramount for appropriate conservative treatment due to the morphologic and immunohistochemical overlap with primary salivary gland carcinomas.

摘要

微囊型/网状神经鞘瘤是一种最近才被描述的神经鞘瘤变体,好发于胃肠道,很少累及头颈部区域。这是首例报道累及下颌下腺的病例。我们报告一例34岁男性,下颌下有一个4.5厘米的肿块。细针穿刺提示为梭形细胞病变。冰冻切片评估提示有黏液表皮样癌的可能。切除标本显示为一个边界清晰、外观呈黏液样的肿块。组织学表现包括有纤维间隔的小叶结构、淋巴细胞-浆细胞浸润以及周边散在的淋巴样聚集物。有两种不同的组织学模式,一种是梭形细胞实性区域,另一种是在黏液样背景中呈微囊型的梭形/卵圆形细胞区域。肿瘤边界呈推挤状,延伸至脂肪组织和相邻实质,无细胞异型性或坏死。免疫组化染色S-100和CD34呈阳性,而钙调蛋白、乳腺珠蛋白、ALK1、p63、雌激素受体、胶质纤维酸性蛋白、平滑肌肌动蛋白、结蛋白、细胞角蛋白7、细胞角蛋白AE1/AE3和C-Kit呈阴性。黏液卡红染色阴性。由于该良性神经鞘瘤变体在形态学和免疫组化方面与原发性涎腺癌有重叠,因此认识到这一点对于采取适当的保守治疗至关重要。

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