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口腔黏膜结节性筋膜炎伴新型 USP6 基因重排:病例报告及文献复习。

Nodular Fasciitis of the Buccal Mucosa with a Novel USP6 Gene Rearrangement: A Case Report and Review of the Literature.

机构信息

Department of Pathology, Rutgers New Jersey Medical School, 150 Bergen Street, Newark, NJ, 07103, USA.

Department of Pathology, Emory University, Atlanta, GA, USA.

出版信息

Head Neck Pathol. 2024 Aug 21;18(1):79. doi: 10.1007/s12105-024-01687-6.

Abstract

Nodular fasciitis is a rare but benign fibroblastic proliferation that typically presents as a solitary lesion with rapid growth and variable mitotic activity. The lesions usually occur on the extremities and occasionally in the head/neck region. Involvement of the buccal mucosa is extremely rare with only few reports in the literature; in this case report, we describe a 41 year old female who presented with a 6-month history of a stable intraoral lump at the junction of the upper and lower lip. Fine needle aspiration revealed an atypical spindle cell population with plump cells. The surgical excision demonstrated a well circumscribed tan-white firm nodule. Histologic examination revealed a spindle cell proliferation that grew in short, intersecting fascicles with focal storiform architecture. The lesion had a pushing border that was not overtly infiltrative and the stroma contained focal myxoid changes giving a "tissue culture" appearance to the cells. Immunohistochemical testing showed the tumor cells were vimentin (+), SMA (+), weakly Calponin (+), and desmin (-), cytokeratin (-), AE1/AE3 (-), S100 (-), ALK (-), STAT6 (-), and beta-catenin (-). Fluorescence in-situ hybridization (FISH) revealed a USP6 gene rearrangement with an atypical probe pattern. Next generation sequencing identified a novel SPTAN1::USP6 fusion gene confirming the diagnosis of buccal nodular fasciitis. Identification of the characteristic histologic features and USP6 gene rearrangements helped support the diagnosis. A review of the literature identified 25 cases of nodular fasciitis involving the buccal mucosa. The occurrence of this tumor in an unusual location may pose difficulties for diagnosis.

摘要

结节性筋膜炎是一种罕见但良性的成纤维细胞增生,通常表现为单一病变,生长迅速,有不同程度的有丝分裂活性。病变通常发生在四肢,偶尔也发生在头颈部。颊黏膜受累极为罕见,文献中仅有少数报道;在本病例报告中,我们描述了一位 41 岁女性,她有 6 个月的稳定的口腔内肿块病史,位于上下唇交界处。细针抽吸显示出典型的梭形细胞群,细胞饱满。手术切除显示出一个界限清楚的棕白色坚实小结节。组织学检查显示出梭形细胞增生,呈短而交错的束状,伴有局灶性束状结构。病变有一个推挤边界,没有明显的浸润性,基质内有局灶性黏液样改变,使细胞呈现出“组织培养”外观。免疫组织化学检测显示肿瘤细胞表达波形蛋白(+)、平滑肌肌动蛋白(+)、弱钙调蛋白(+)和结蛋白(-),细胞角蛋白(-)、AE1/AE3(-)、S100(-)、ALK(-)、STAT6(-)和β-连环蛋白(-)。荧光原位杂交(FISH)显示 USP6 基因重排,出现异常探针模式。下一代测序确定了一种新型 SPTAN1::USP6 融合基因,证实了颊部结节性筋膜炎的诊断。特征性组织学特征和 USP6 基因重排的鉴定有助于支持诊断。文献复习发现 25 例累及颊黏膜的结节性筋膜炎。该肿瘤发生在不常见的部位可能会给诊断带来困难。

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