隆突性皮肤纤维肉瘤的临床病理分析:附28例报告  

Clinicophathologic Analysis of 28 Cases of Dermatofibrosarcoma Protuberans

作　　者：翁洁玲[1] 欧阳小明[1] 郝卓芳[1] 黄世章[1] 廖德贵[1] 梅开勇[1] 

机构地区：[1]广州医科大学附属第二医院病理科,广东广州510260

出　　处：《分子影像学杂志》2015年第4期356-358,共3页Journal of Molecular Imaging

摘　　要：目的探讨隆突性皮肤纤维肉瘤的临床病理特征。方法对28例隆突性皮肤纤维肉瘤从临床表现、病理形态及免疫组化等方面进行观察分析。结果 28例隆突性皮肤纤维肉瘤好发于中青年男性,临床多表现为皮肤固定的结节状肿物,手术切除不完全易局部复发。病理组织学表现为梭形细胞排列成典型的车辐状或席纹状。免疫组化所有病例Vimentin及CD34均阳性,S-100均阴性。其中2例局部伴高级别肉瘤转化,转化区域CD34表达减弱或不均匀。结论 CD34有助于DFSP与其他皮肤梭形细胞肿瘤的鉴别,当CD34表达减弱时需注意观察是否局部伴高级别肉瘤转化。Objective To study the clinicophathologic characteristics of dermatofibrosarcoma protuberans(DFSP). Methods Clinical pathological features and immunohistochemical findings were observed in 28 cases of DFSP. Results The majority of the patients were young to middle-aged men. The tumor usually presented as a firm nodule, with a high frequency of recurrence after incomplete excision. The spindle-shaped cells were typically arranged in a storiform or a cartwheel growth pattern. In this study, all cases of DFSPs tended to stain positively for Vimentin and CD34 and negatively for S-100. DFSP with high-grade sarcomatous transformation was observed in 2 cases, in which CD34 was weak. Conclusion CD34 is helpful for us to distinguish DFSP from other cutaneous spindle cell tumors. When CD34 is weak or uneven in some areas, attention should be paid to observing if the DFSP contains a high-grade sarcomatous component.

关 键 词：隆突性皮肤纤维肉瘤 免疫组化 鉴别诊断 

分 类 号：R739.5[医药卫生—肿瘤]