期刊文献+

原发性阴茎尤因肉瘤一例报告 被引量:1

A case report of primary Ewing's sarcoma of penis
原文传递
导出
摘要 尤因肉瘤是尤因肉瘤肿瘤家族(ESFT)中的一员,通常起源于骨和软组织,发生于阴茎者罕见。本文报道1例21岁的阴茎左侧尤因肉瘤患者。行阴茎肿物切除术后,病理诊断为尤因肉瘤,切缘阳性,再次行根治性阴茎全切术。术后经过14个周期化疗,未行放疗。随访8个月无局部复发及转移。 Ewing sarcoma is a member of the Ewing sarcoma family tumor(ESFT),which is commonly from bones and soft tissues,while it is rare for penis.In this thesis,a case of 21-year-old Ewing sarcomas on the left side of the penis was reported.After the penis mass excision,the pathological diagnosis was Ewing sarcoma and positive margin,then he underwent penis total hysterectomy.After the surgery,he received chemotherapy for 14 cycles without radiation.With 8 months' reexamination and follow-up,there was no local recurrence or metastasis.
作者 邱娴娴 赵银银 江克华 唐小虎 孙发 Qiu Xianxian;Zhao Yin-yin;Jiang Kehua;Tang Xiaohu;Sun Fa(Department of Urology,Guizhou Province People's Hospital,Guiyang 550002,China)
出处 《中华泌尿外科杂志》 CAS CSCD 北大核心 2020年第9期707-708,共2页 Chinese Journal of Urology
关键词 阴茎肿瘤 尤因肉瘤 病例报告 Penile neoplasm Ewing sarcoma Case reports
  • 相关文献

参考文献3

二级参考文献15

  • 1艾平,王瑾,王辛.骨外尤文氏肉瘤15例临床及病理分析[J].四川医学,2006,27(9):946-947. 被引量:11
  • 2Parham DM, Roloson GJ, Feely M, et al. Primary malignant neuroepithelial tumors of the kidney : a clinicopathologic analysis of 146 adult and pediatric cases from the National Wilms' Tumor Study Group Pathology Center. Am J Surg Pathol, 2001, 25 : 133-146.
  • 3Jimenez RE, Folpe AL, Lapham RL, et al. Primary Ewing's sar- coma/primitive neuroectodermal tumor of the kidney: a clinico- pathologic and immunohistochemical analysis of 11 cases. Am J Surg Pathol, 2002, 26: 320-327.
  • 4Bing Z, Zhang P, Tomaszewski JE, et al. Primary Ewing sarco- ma/primitive neuroectodermal tumor of the kidney. J Urol, 2009, 181 : 1341-1342.
  • 5Kartg MS, Yoou HK, Choi JB, et al. Extraskeletal Ewlng's sar- coma of the hard palate. J Korean Med Sci. 2005,20 : 687-690.
  • 6Folpe AL, Hill CE, Parham DM, et al. Immunohistoehemical detection of FLI-1 protein expression: a study of 132 round cell tumors with emphasis on CD99-positive mimics of Ewing's saroo- ma/primitive neuroectodermal tumor. Am J Surg Pathol, 2000, 24 : 1657-1662.
  • 7Nilsson G, Wang M, Wejde J, et al. Detection of EWS/FLI-1 by immunostaining. An adjunctive tool in diagnosis of Ewing's sarcoma and primitive neuroectodermal tumor on cytologic sam- ples and paraffin-embedded archival material. Sarcoma, 1999, 3 : 25-32.
  • 8Bamoud R, Sabourin JC, Pasquier D, et al. Immunohistochemi- cal expression of WT1 by desmoplastic smal round cell tumor: a comparative study with other small round cell tumors. Am J Surg Pathol, 2000, 24: 830-836.
  • 9Hill DA, Pfeifer JD, Marley EF, et al. WT1 staining reliably differentiates desmoplastic small round cell tumor from Ewing's sarcoma/primitive neuroectodermal tumor. An immunohistochem- ieal and molecular diagnostic study. Am J Clin Pathol, 2000, 114 : 345-353.
  • 10Mukhopadhyay P, Gairola M, Sharma MC, et al. Primary spinal epidural extraosseous Ewing's Sarcoma: report of five cases and literature review. Australas Radiol, 2001, 45 : 372-379.

共引文献13

同被引文献9

引证文献1

二级引证文献3

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