Department of Pathology, University of Virginia Medical Center, Charlottesville, VA 22908-0214, USA.
Int J Gynecol Pathol. 2010 Nov;29(6):600-4. doi: 10.1097/PGP.0b013e3181e31f94.
Proximal epithelioid sarcoma is an extremely uncommon lesion of the vulva, with the potential for aggressive behavior. We report a case of this entity and discuss its relationship to the epithelial-type "malignant rhabdoid tumor" (MRT) of the soft tissue. On the basis of a review of the pertinent information on both these entities, it is concluded that they likely represent biologically different but morphologically and immunohistochemically similar neoplasms. Both proximal epithelioid sarcoma and MRT comprise epithelioid cells with densely eosinophilic cytoplasmic inclusions, and they each lack the INI1 gene product. Nevertheless, the literature suggests that other selected genetic differences between the 2 lesions, and the more rapid and aggressive course of MRT distinguish these tumor types as separate clinicopathologic entities.
外阴部的近端上皮样肉瘤是一种非常罕见的病变,具有侵袭性行为的潜力。我们报告了一例该实体,并讨论了其与软组织上皮型“恶性横纹肌样瘤”(MRT)的关系。基于对这两种实体的相关信息的回顾,得出的结论是它们可能代表生物学上不同但形态学和免疫组织化学上相似的肿瘤。近端上皮样肉瘤和 MRT 均由具有浓密嗜酸性细胞质包涵物的上皮样细胞组成,并且它们均缺乏 INI1 基因产物。然而,文献表明,这两种病变之间的其他一些遗传差异,以及 MRT 更快速和侵袭性的病程,将这两种肿瘤类型区分开来,作为独立的临床病理实体。