Ding J, Hashimoto H, Enjoji M
Second Department of Pathology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Cancer. 1989 Aug 1;64(3):721-9. doi: 10.1002/1097-0142(19890801)64:3<721::aid-cncr2820640326>3.0.co;2-q.
Nine cases of dermatofibrosarcoma protuberans with fibrosarcomatous areas (DFSP with FS) were analyzed clinicopathologically, and the findings compared with allied tumors comprising 43 cases of ordinary DFSP, ten of superficial fibrosarcoma (SFS), and 11 of storiform variant of malignant fibrous histiocytoma (SV MFH). All but one case of DFSP with FS developed on the trunk of the body. Eight of the nine patients (89%) had one recurrence with a shorter prerecurrent interval than that of the ordinary DFSP, and a hipbone metastasis was identified in one patient. These findings reflect the unfavorable course, in contrast to the ordinary DFSP. Microscopically, the FS areas were presented either in the initial lesion (five cases) or in the recurrent one (four cases), areas showing cellularity, mitotic figures, and cytologic anaplasia that exceeded those in the DFSP areas. Dermatofibrosarcoma protuberans with FS and allied categories such as SFS and SV MFH shared various clinical and histologic features but there was a diversity in the prognosis relative to the grade of malignancy. The relationship between DFSP with FS and the allied tumors was given attention.
对9例伴有纤维肉瘤区域的隆突性皮肤纤维肉瘤(DFSP伴FS)进行了临床病理分析,并将结果与相关肿瘤进行比较,相关肿瘤包括43例普通DFSP、10例浅表纤维肉瘤(SFS)和11例恶性纤维组织细胞瘤的席纹状变型(SV MFH)。除1例DFSP伴FS外,其余均发生于身体躯干。9例患者中有8例(89%)复发1次,复发前间隔时间比普通DFSP短,1例患者出现髋骨转移。与普通DFSP相比,这些结果反映了其预后不良。显微镜下,FS区域出现在初始病变中(5例)或复发病变中(4例),这些区域的细胞密度、有丝分裂象和细胞学间变超过了DFSP区域。伴有FS的隆突性皮肤纤维肉瘤以及SFS和SV MFH等相关类型具有多种临床和组织学特征,但相对于恶性程度而言预后存在差异。关注了DFSP伴FS与相关肿瘤之间的关系。