期刊文献+

隆突性皮肤纤维肉瘤的MRI诊断价值研究 被引量:2

Research for Diagnostic Significance of MRI in Dermatofibrosarcoma protuberans
原文传递
导出
摘要 目的分析隆突性皮肤纤维肉瘤(DFSP)的MRI表现,探讨MRI对DFSP的诊断价值。方法回顾性分析12例经病理证实的DFSP患者的影像资料,男7例、女5例,总结其影像特点。结果 12例病变位置均较表浅,3例与皮肤分界不清,9例分界清,其中8例与皮肤间距离〈3 mm,1例〉5 mm。病变大小3.2~15.6 cm,平均8cm。病变形态呈扁丘状、卵圆形、分叶状,3例呈多结节聚合状,1例见子结节外突。与肌肉相比,在T1WI上3例呈稍低信号,5例呈等信号,4例呈稍高信号;在T2WI上11例呈高信号,1例为稍高信号。6例行增强检查,5例明显强化,1例呈中度强化。结论 DFSP的MRI表现具有一定特征性,MRI检查可帮助其诊断。 Objective To explore the diagnostic significance of MRI in dermatofibrosarcoma protuberans( DFSP) by analyzing MRI imaging features of DFSP. Methods Analyze MRI images of 12 lesions confirmed as DFSP by pathology,including 7 male and 5 female. Results All 12 lesions are superficial and very adjacent to the skin. There is no clear limit between 3 lesions and skin. In the remaining 9 lesions,there is a clear limit. In these 9 lesions,the distance between8 lesions and skin is less than 3 mm,but only 1 lesion has a distance more than 5 mm. The maximum diameters of 12 lesions vary within the range between 3. 2 cm and 15. 6 cm( 8 cm on average). The 12 lesions have various morphology( flat dune-like,oval and lobular). 3 lesions are multi-nodular,and l lesion has outward sub-nodule. Compared to muscles,3lesions are slightly hypointense on T1 WI,5 lesions isointense,4 lesions slightly hyperintense. 11 lesions are hyperintense on T2 WI,while 1 lesion is slightly hyperintense. In 6 enhanced lesions,5 lesions are strongly enhancing while 1 lesion is moderate. Conclusion DFSP have characteristic features in MRI,and MRI examination can help diagnose DFSP.
出处 《临床放射学杂志》 CSCD 北大核心 2016年第9期1419-1421,共3页 Journal of Clinical Radiology
关键词 隆突性皮肤纤维肉瘤 诊断 MRI Dermatofibrosarcoma protuberans Diagnosis MRI
  • 相关文献

参考文献10

二级参考文献68

  • 1白秉学,徐东刚,范明.碱性成纤维细胞生长因子的研究进展[J].国外医学(遗传学分册),2004,27(4):197-199. 被引量:22
  • 2杨连君,司晓辉.隆突性皮肤纤维肉瘤的病理特点及其鉴别诊断[J].临床误诊误治,2005,18(12):904-906. 被引量:14
  • 3周晓莉,范钦和.隆突性皮肤纤维肉瘤分子遗传学研究进展[J].中华病理学杂志,2006,35(1):44-47. 被引量:7
  • 4林上奇,鲁西,吴宝珊.颈部隆突性皮肤纤维肉瘤二例[J].中华放射学杂志,1996,30(10):716-716. 被引量:2
  • 5[1]Enzinger FM,Weiss SW. Fibrohistiocytic tumours of intermediate malignancy. In:Enzinger FM, Weiss SW, eds. Soft tissue tumors. 3rd ed,St Louis: Mosby CV,1995:325~48.
  • 6[2]Calonje E,Fletcher CDM. Myxoid differentiation in dermatofibrosarcoma protuberans and its fibrosarcomatous variant:clinicopathologic analysis of 5 cases.J Cutan Pathol,1996,23:30~6.
  • 7[3]Connelly JH,Evans HL. Dermatofibrosarcoma protuberans. A clinicopathological review with emphasis on fibrosarcomatous areas. Am J Surg Pathol,1992,16:921.
  • 8[4]Betti R,Inselvini E,Crosti C. Unusal features of primary dermatofibrosarcoma protuberans and its myxoid recurrence. J Cutan Pathol,1996,23:283~7.
  • 9[5]Frierson HF,Cooper PH.Myxoid variant of dermatofibrosarcoma protuberans.Am J Surg Pathol,1983,7:445.
  • 10[7]Shmookler BM,Enzinger FM,Weiss SW. Giant cell fibroblastoma. A juvenile form of dermatofibrosarcoma protuberans. Cancer,1989,64:2154.

共引文献63

同被引文献20

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部