MacKinnon William F, Carter Michael D, Bridge Julia A, Tremaine Robert D, Walsh Noreen M G
Department of Pathology and Laboratory Medicine, Nova Scotia Health Authority, Halifax, Nova Scotia, Canada.
Department of Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.
J Cutan Pathol. 2019 Jun;46(6):421-424. doi: 10.1111/cup.13450. Epub 2019 Apr 3.
Cutaneous syncytial myoepithelioma (CSM) is a recently recognized, histopathological variant of myoepithelial (ME) tumors of the skin. It is characterized by a syncytial arrangement of spindled, ovoid, and/or epithelioid cells forming a well-circumscribed, unencapsulated dermal nodule. There is a paucity of intervening stroma, and absent duct or gland formation. Strong immunohistochemical staining for S100 and epithelial membrane antigen (EMA) has been described, while cytokeratin expression has been uncommon. The majority of CSMs harbor a rearrangement involving the EWSR1 gene. Although various fusion partner genes have been discovered in ME tumors at other anatomic sites, none has yet been described in CSM. We present a case of CSM represented clinically by a papule on the mid-upper back of a healthy 44-year-old female. It exhibited morphological and immunohistochemical features of a CSM with strong, diffuse S100 and alpha-actin expression, and focal positivity for EMA and cytokeratin AE1/AE3. Fluorescence in-situ hybridization showed an EWSR1 gene rearrangement. Massively parallel next-generation RNA sequencing revealed PBX3 as the fusion partner. The EWSR1-PBX3 gene fusion has been previously identified in three cases of ME tumors of bone and soft tissue, and in a case of retroperitoneal leiomyoma. This is the first report of an EWSR1-PBX3 fusion in CSM.
皮肤合体性肌上皮瘤(CSM)是一种最近才被认识的皮肤肌上皮(ME)肿瘤的组织病理学变异型。其特征是梭形、卵圆形和/或上皮样细胞呈合体状排列,形成一个边界清楚、无包膜的真皮结节。其间质稀少,无导管或腺体形成。已有文献报道其对S100和上皮膜抗原(EMA)有强免疫组化染色,而细胞角蛋白表达不常见。大多数CSM存在涉及EWSR1基因的重排。尽管在其他解剖部位的ME肿瘤中已发现各种融合伴侣基因,但在CSM中尚未见报道。我们报告一例CSM,临床表现在一名44岁健康女性的中上背部丘疹。它表现出CSM的形态学和免疫组化特征,S100和α-肌动蛋白呈强弥漫性表达,EMA和细胞角蛋白AE1/AE3呈局灶阳性。荧光原位杂交显示EWSR1基因重排。大规模平行下一代RNA测序显示PBX3为融合伴侣。EWSR1-PBX3基因融合先前已在3例骨和软组织ME肿瘤以及1例腹膜后平滑肌瘤中被鉴定。这是CSM中EWSR1-PBX3融合的首次报道。