Department of Pathology, Rutgers New Jersey Medical School, 150 Bergen Street, Newark, NJ, 07103, USA.
Department of Pathology, Emory University, Atlanta, GA, USA.
Head Neck Pathol. 2024 Aug 21;18(1):79. doi: 10.1007/s12105-024-01687-6.
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.
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。