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肾脏巨大尤因肉瘤/原始神经外胚叶肿瘤1例及文献复习 被引量：5

A huge Ewing’s sarcoma/primitive neuroectodermal tumor in kidney: a case report and literature review
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摘要 尤因肉瘤（Ewing’s sarcoma）/原始神经外胚叶肿瘤（primitive neuroectodermal tumor,PNET）是指包括骨和软组织尤因肉瘤、Askin瘤和原始神经外胚叶肿瘤等在内的一族小细胞恶性肿瘤,多发生于长骨及骨盆,发生于肾脏的较罕见。有文献对35例肾尤因肉瘤/原始神经外胚叶肿瘤的报道显示[1],该病的发病年龄主要在4～69岁,
作者 毛顿 谭政 廖琼 廖洪 李曾 肖英明 吴毅
机构地区 四川省第二人民医院、四川省肿瘤医院泌尿外科 四川省第二人民医院、四川省肿瘤医院病理科
出处 《肿瘤》 CAS CSCD 北大核心 2012年第10期851-853,共3页 Tumor
关键词 肾肿瘤 肉瘤 Ewing 神经外胚层瘤 病理学 临床 Kidney neoplasms； Sarcoma, Ewing’s； Neuroectodermal tumors； Pathology, clinical
分类号 R735.35 [医药卫生—肿瘤]
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参考文献6

  • 1ANGELJ R, ALFRED A, SAKHUJA A, etal. Ewing's sarcoma of the kidney[J]. IntJ Clin Oncol, 201 O, 15(3):314-318.
  • 2POMARA G, CAPPELLA F, CUTTANO M G, et al. Primitive neuroectodermal tumor (PNET) of the kidney: a case report[J]. BMC Cancer, 2004, 4:3.
  • 3MARLEY E F, LIAPIS H, HUMPHREY P A, et al. Primitive neuroectodermal tumor of the kidney-another enigma:a pathologic, immunohistochemical,and molecular diagnostic study[J]. AmJ Surg Pathol, 1997, 21(3):354-359.
  • 4PARHAM D M, ROLOSON G J, 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(2):133-146.
  • 5JUAN C J, WU C J,CHEN C Y, et al. Primitive neuroectodermal tumor of the Kidney associated with Budd-Chiari syndrome in a 17-year-old girl[J].J Formos MedAssoc, 2001, 100(9):628-630.
  • 6THYAVIHALLY Y B, TONGAONKAR H B, GUPTA S, et al. Primitive neuroectodermal tumor of the kidney: a single institute series of 16 patients[J]. Urology, 2008, 71(2):292-296.

同被引文献70

  • 1LISSAT A, CHAO M M, KONTNY U. Targeted therapy in Ewing sarcoma[J]. ISRN Oncol, 2012,2012:609439.
  • 2LUDWIG J A. Ewing sarcoma: historical perspectives, current state-of-the-art, and opportunities for targeted therapy in the future[J]. Curt Opin Oncol, 2008, 20(4):412-418.
  • 3RIGGI N, STAMENKOVlC I. The BioJogy of Ewing sarcoma[J]. Cancer lett, 2007, 254(1 ):1 - 10.
  • 4SANKAR S, LESSNICK S L. Promiscuous partnerships in Ewing's sarcoma[J]. Cancer Genet, 2011, 204(7):351-365.
  • 5NG T L, O'SULLIVAN M J, PALLEN C J, et al. Ewing sarcoma with novel translocation t(2;16) producing an in-frame fusion of FUS and FEV[J]. J Mol Diagn, 2007, 9(4):459-463.
  • 6TAN A Y, MANLEY J L. The TET family of proteins: functions and ro(es in disease[J]. J Mol Cell &iol, 2009, 1 (2):82-92.
  • 7SETH A, WATSON D K. ETS transcription factors and their emerging roles in human cancer[j]. EurJ Cancer, 2005, 41 (16):2462-2478.
  • 8SZUHAI K, USZENGA M, DE JONG D, et al. The NFATc2gene is involved in a novel cloned translocation in a Ewing sarcoma variant that couples its function in immunology to oncology[j]. C/in Cancer Res, 2009, 15(7):2259-2268.
  • 9CHEW J L, LOH Y H, ZHANG W, et al. Reciprocal transcriptional regulation of Pou5fl and Sox2 via the Oct4/Sox2 complex in embryonic stem cells[J]. Mol Cell Biol, 2005, 25(14):6031-6046.
  • 10SUMEGI J, NISHIO J, NELSON M, et al. A novel t(4;22)(q31 ;ql 2) produces an EWSR1-SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor[J]. Mod Pathol, 2011,24(3):333-342.

引证文献5

二级引证文献19

肿瘤
2012年 第10期

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