Cheng S D, Usmani A S, DeYoung B R, Ly M, Pellegrini A E
The Ohio State University, University Medical Center, Columbus, USA.
J Cutan Pathol. 2001 Jan;28(1):49-52. doi: 10.1034/j.1600-0560.2001.280106.x.
There have been several reports in the literature of dermatofibromas with granular cells. Here we report a granular cell tumor with the architecture of a dermatofibroma. This is the first report of this histological variant of granular cell tumor. The lesion was a 2.5-cm oval, hyperpigmented plaque present for "years" on the back of a 60-year-old African-American woman.
The specimen was processed using formalin fixation and paraffin embedding. Tissue sections were stained with hematoxylin and eosin. Immunohistochemical studies were performed with antibodies directed against S-100 protein, neuron-specific enolase, and factor XIIIa.
Histopathologic examination revealed granular cells, some of which were spindle shaped, distributed singly and in small groups between collagen bundles resembling a dermatofibroma. Immunohistochemical studies showed the tumor cells to be positive for S-100 and neuron-specific enolase and negative for factor XIIIa.
The immunohistochemical findings support the diagnosis of a granular cell tumor with a dermatofibroma-like pattern.
文献中有几篇关于伴有颗粒细胞的皮肤纤维瘤的报道。在此,我们报告一例具有皮肤纤维瘤结构的颗粒细胞瘤。这是颗粒细胞瘤这种组织学变异型的首例报道。该病变为一名60岁非裔美国女性背部出现“数年”的2.5厘米椭圆形色素沉着斑。
标本采用福尔马林固定和石蜡包埋处理。组织切片用苏木精和伊红染色。使用针对S-100蛋白、神经元特异性烯醇化酶和因子XIIIa的抗体进行免疫组织化学研究。
组织病理学检查显示有颗粒细胞,其中一些呈梭形,单个或小群分布于胶原束之间,类似皮肤纤维瘤。免疫组织化学研究显示肿瘤细胞S-100和神经元特异性烯醇化酶呈阳性,因子XIIIa呈阴性。
免疫组织化学结果支持诊断为具有皮肤纤维瘤样模式的颗粒细胞瘤。