非典型纤维黄瘤
病理
皮肤纤维瘤
隆突性皮肤纤维肉瘤
颗粒细胞瘤
多形性(细胞学)
平滑肌肉瘤
波形蛋白
川地68
血管肉瘤
皮肤纤维肉瘤
S100蛋白
颗粒细胞
免疫组织化学
平滑肌瘤
巨细胞
组织发生
生物
医学
中枢神经系统
神经科学
作者
Sarah N. Rudisaile,Mark A. Hurt,Daniel J. Santa Cruz
标识
DOI:10.1111/j.0303-6987.2005.00326.x
摘要
Abstract: We report on two patients with granular cell atypical fibroxanthoma. Both neoplasms were solitary, light‐tan, dome‐shaped papules on sun‐exposed areas of the head in two elderly white men. Microscopically, these neoplasms showed a dermal proliferation of pleomorphic granular cells with irregular hyperchromatic nuclei, multinucleated cells, and scattered mitoses. Immunohistochemical stains were positive for CD68 and vimentin and negative for Melan‐A or human melanoma black (HMB)‐45, S‐100 protein, pancytokeratin, and actin, consistent with atypical fibroxanthoma. The differential diagnosis of granular cells in neoplasms containing cytological pleomorphism is challenging in view of the many different neoplasms that may present with granular cytoplasm. These include the conventional granular cell tumor and its malignant form, leiomyoma, leiomyosarcoma, dermatofibroma, dermatofibrosarcoma protuberans, and angiosarcoma.
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