伴有新型 USP6 基因重排的颊黏膜结节性筋膜炎:病例报告和文献综述。

IF 3.2 Q2 PATHOLOGY
Mallissa Vuong, Haider A Mejbel, Alexander C Mackinnon, Dylan Roden, David I Suster
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引用次数: 0

摘要

结节性筋膜炎是一种罕见的良性成纤维细胞增生,通常表现为单发病变,生长迅速,有丝分裂活动不稳定。病变通常发生在四肢,偶尔也会发生在头颈部。累及口腔粘膜的病例极为罕见,文献中也鲜有报道;在本病例报告中,我们描述了一名 41 岁女性的病史,她在 6 个月前发现上下唇交界处有一个稳定的口腔内肿块。细针穿刺显示其为非典型纺锤形细胞群,细胞丰满。手术切除后发现一个周界清楚的棕白色坚实结节。组织学检查显示,纺锤形细胞增生呈短小、交叉的束状生长,具有局灶性星状结构。病灶边界呈推移状,没有明显浸润,基质中含有局灶性肌样改变,使细胞呈现出 "组织培养 "的外观。免疫组化检测显示,肿瘤细胞为波形蛋白(+)、SMA(+)、弱钙蛋白(+)、desmin(-)、细胞角蛋白(-)、AE1/AE3(-)、S100(-)、ALK(-)、STAT6(-)和β-catenin(-)。荧光原位杂交(FISH)发现 USP6 基因重排,探针模式不典型。下一代测序发现了一个新的 SPTAN1::USP6 融合基因,确诊为颊结节性筋膜炎。特征性组织学特征和 USP6 基因重排的鉴定有助于支持诊断。通过查阅文献,发现有 25 例涉及颊粘膜的结节性筋膜炎病例。这种肿瘤发生在不寻常的部位可能会给诊断带来困难。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nodular Fasciitis of the Buccal Mucosa with a Novel USP6 Gene Rearrangement: A Case Report and Review of the Literature.

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.

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来源期刊
CiteScore
5.70
自引率
9.50%
发文量
99
期刊介绍: Head & Neck Pathology presents scholarly papers, reviews and symposia that cover the spectrum of human surgical pathology within the anatomic zones of the oral cavity, sinonasal tract, larynx, hypopharynx, salivary gland, ear and temporal bone, and neck. The journal publishes rapid developments in new diagnostic criteria, intraoperative consultation, immunohistochemical studies, molecular techniques, genetic analyses, diagnostic aids, experimental pathology, cytology, radiographic imaging, and application of uniform terminology to allow practitioners to continue to maintain and expand their knowledge in the subspecialty of head and neck pathology. Coverage of practical application to daily clinical practice is supported with proceedings and symposia from international societies and academies devoted to this field. Single-blind peer review The journal follows a single-blind review procedure, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous. Single-blind peer review is the traditional model of peer review that many reviewers are comfortable with, and it facilitates a dispassionate critique of a manuscript.
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