Sasaki M, Ishida T, Horiuchi H, MacHinami R
Department of Pathology, Faculty of Medicine, The University of Tokyo, Japan.
Pathol Int. 1999 Sep;49(9):799-806. doi: 10.1046/j.1440-1827.1999.00944.x.
The aim of this study is to evaluate the degree and spectrum of malignancy of dermatofibrosarcoma protuberans (DFSP) in the aspect of proliferative activity, flow cytometric DNA analysis, and p53 immunoreactivity. Twenty-three tumors from 19 cases of DFSP including three cases of DFSP with fibrosarcomatous areas (DFSP-FS) were studied in comparison with its allied fibrohistiocytic tumors; that is, dermatofibroma (DF; 46 cases), fibrosarcoma (FS; four cases), and malignant fibrous histiocytoma (MFH; 11 cases). MIB-1 labeling index (LI) of DFSP was significantly higher than that of DF and was lower than those of FS and of MFH. In ordinary DFSP, the recurrent tumors exhibited significantly higher MIB-1 LI than that of the primary tumors, whereas the primary tumors showed almost the same proliferative activity of DF. DFSP-FS tended to have a higher proliferative activity than DFSP without FS-area (ordinary DFSP). In five of 19 cases of DFSP, aneuploidy (near-diploidy) was found in four recurrent and one primary tumors. Immunohistochemical p53 overexpression was found in three of 19 cases of DFSP which also showed higher proliferative activity and aneuploidy. All cases of DF were immunohistochemically negative for p53, but most of the cases of FS and MFH were positive. Although DFSP has been classified in a category of fibrohistiocytic tumor of intermediate malignancy, the recurrent DFSP, DFSP-FS, and DFSP with aneuploidy and/or p53 overexpression could be a subgroup of DFSP with more aggressive clinical behavior than ordinary primary ones.
本研究旨在从增殖活性、流式细胞术DNA分析及p53免疫反应性方面评估隆突性皮肤纤维肉瘤(DFSP)的恶性程度及范围。对19例DFSP患者的23个肿瘤进行了研究,其中包括3例伴有纤维肉瘤区域的DFSP(DFSP-FS),并与其相关的纤维组织细胞肿瘤进行比较,即皮肤纤维瘤(DF;46例)、纤维肉瘤(FS;4例)和恶性纤维组织细胞瘤(MFH;11例)。DFSP的MIB-1标记指数(LI)显著高于DF,低于FS和MFH。在普通DFSP中,复发性肿瘤的MIB-1 LI显著高于原发性肿瘤,而原发性肿瘤的增殖活性与DF几乎相同。DFSP-FS的增殖活性往往高于无纤维肉瘤区域的DFSP(普通DFSP)。在19例DFSP患者中,有5例在4个复发性肿瘤和1个原发性肿瘤中发现非整倍体(近二倍体)。在19例DFSP患者中有3例发现免疫组化p53过表达,这些病例也表现出较高的增殖活性和非整倍体。所有DF病例的p53免疫组化均为阴性,但大多数FS和MFH病例为阳性。尽管DFSP已被归类为中度恶性的纤维组织细胞肿瘤,但复发性DFSP、DFSP-FS以及伴有非整倍体和/或p53过表达的DFSP可能构成DFSP的一个亚组,其临床行为比普通原发性DFSP更具侵袭性。