Hirashima Noriyuki, Misago Noriyuki, Shinogi Taro, Inoue Takuya, Miura Yoshihiro, Narisawa Yutaka
Division of Dermatology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
J Dermatol. 2006 Jul;33(7):486-8. doi: 10.1111/j.1346-8138.2006.00114.x.
Atrophic dermatofibrosarcoma protuberans (atrophic DFSP) is a variant of dermatofibrosarcoma protuberans (DFSP), and is clinically characterized by depressed lesions. We report a patient with a typical atrophic DFSP lesion with marked eosinophilic infiltration. The patient was a 55-year-old woman with a dark-red, depressed lesion in the epigastric region. Histopathological examination of the lesion showed proliferation of fibroblast-like cells in a storiform pattern in the dermis and subcutaneous tissue. Immunohistochemical staining of tumor cells was positive for CD34. The lesion was histopathologically typical of DFSP, but no elevated lesion was clinically observed. Thus, a diagnosis of atrophic DFSP was made. Moreover, this tumor tissue exhibited marked eosinophilic infiltration. To our knowledge, they are no reports of eosinophilic infiltration in DFSP tissue. Therefore, this seems to be an extremely rare case of DFSP.
萎缩性隆突性皮肤纤维肉瘤(atrophic DFSP)是隆突性皮肤纤维肉瘤(DFSP)的一种变体,临床特征为凹陷性病变。我们报告一例典型的伴有显著嗜酸性粒细胞浸润的萎缩性DFSP病变患者。该患者为一名55岁女性,上腹部有一个暗红色凹陷性病变。病变的组织病理学检查显示真皮和皮下组织中呈束状排列的成纤维细胞样细胞增生。肿瘤细胞的免疫组化染色CD34呈阳性。该病变在组织病理学上是典型的DFSP,但临床上未观察到隆起性病变。因此,诊断为萎缩性DFSP。此外,该肿瘤组织表现出显著的嗜酸性粒细胞浸润。据我们所知,尚无DFSP组织中嗜酸性粒细胞浸润的报道。因此,这似乎是一例极其罕见的DFSP病例。