Ríos-Martín Juan José, Delgado Mario Díaz, Moreno-Ramírez David, García-Escudero Antonio, González-Cámpora Ricardo
Department of Pathology, Virgen Macarena University Hospital, Seville, Spain.
Am J Dermatopathol. 2007 Feb;29(1):84-7. doi: 10.1097/01.dad.0000246175.73447.3a.
Two cases of an uncommon histopathological variant of atypical fibroxanthoma (AFX) are described. Even though both lesions presented as clinically conventional atypical fibroxanthoma, histopathology disclosed a neoplasm composed of cells with granular change that was negative for S100 staining, and showed prominent pleomorphism, severe nuclear atypia, and a high mitotic index. Degenerative change may explain the granular phenotype in these two cases of AFX. The differential diagnosis with primitive nonneural granular cell tumor is discussed.
本文描述了两例非典型纤维黄色瘤(AFX)的罕见组织病理学变异型病例。尽管这两个病变在临床上均表现为典型的非典型纤维黄色瘤,但组织病理学显示肿瘤由S100染色阴性的颗粒状细胞组成,具有明显的多形性、严重的核异型性和高有丝分裂指数。退行性改变可能解释了这两例AFX的颗粒表型。文中还讨论了与原始非神经颗粒细胞瘤的鉴别诊断。