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儿童先天性中胚层肾瘤的超微结构观察 被引量:2

The ultrastructural studies on congenital nesoblastic nephroma of children
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摘要 本文观察了儿童先天性中胚层肾瘤(CMN)6例,其中典型CMN5例,富于细胞型(或不典型)CMN1例。光镜见CMN酷似平滑肌瘤或纤维肉瘤。电镜下CMN的两型瘤细胞都分化良好,并具有向纤维母细胞或肌纤维母细胞分化的特点。术后1例复发,5例随访至1至15年无肿瘤生存。 \ \ Six cases of chilerens congenital mesoblastic nephroma(CMN)were studied,including five typical CMN,and the other one fully cellular type(or atypical).The CMN is histologically similar to fibrosarcoma or Leiomyoma.Ultrastructurally,there are benign features with consistent myofibroblastic of fibroblastic differentiation.After the surgical operation,only one case suffered recrudescence.While remaining 5 cases following one to fivteen years,stll living without tunor. \ \
出处 《重庆医科大学学报》 CAS CSCD 1997年第1期52-54,共3页 Journal of Chongqing Medical University
关键词 先天性 中胚层肾瘤 超微结构 儿童 CMN Ultrastructural
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同被引文献16

  • 1周晓岩,王琳,冯畹兰.先天性中胚层肾瘤的流式细胞术分析及其与肾母细胞瘤的比较[J].中华小儿外科杂志,1995,16(5):284-285. 被引量:2
  • 2殷敏智,张忠德,周中和.后肾间质肿瘤的病理观察[J].中华病理学杂志,2006,35(2):97-100. 被引量:7
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  • 5Loeb DM, Hill DA, Dome JS. Complete response of recurrent cellular congenital mesoblastic nephroma to chemotherapy [ J ]. J Pediatr Hematol Oncol,2002,24(6) :478 - 481.
  • 6Kumar S, Carr T, Marsden HB, et al, Study of childhood renal tumours using peroxidase conjugated lectins[J]. J Clin Pathol, 1986,39(7): 736- 741.
  • 7Morrison KB, Tognon CE, Garnett MJ, et al. ETV6-NTRK3 transformation requires insulin-like growth factor 1 receptor signaling and is associated with constitutive IRS-1 tyrosine phosphorylation[J]. Oncogene, 2002,21 (3) :5684 - 5695.
  • 8Rubin BP, Chen CJ, Morgan TW, et al. Congenital mesoblastic nephroma t(12; 15) is associated with ETV6-NTRK3 gene fusion[J]. Am J Pathol, 1998,153(5) : 1451 - 1458.
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