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小儿先天性纤维肉瘤一例报道并文献复习 被引量:2

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摘要 1病例报告 患儿男,4d,G3P3,足月剖宫产。因发现左前臂巨大红色肿物4d入院。患儿出生时即被发现左前臂有一红色巨大肿物,肿物表面发亮,患儿能自行抬起左前臂,左手指可活动。出生后肿物无明显增大。体检:一般情况可,营养中等,头颈胸腹未见异常,左前臂可见一大小约8cm×7cm×6cm的椭圆形红色肿物,表面皮肤紧张、发亮,触之呈囊实性,质软偏中,
出处 《中华肿瘤防治杂志》 CAS 2011年第23期1887-1888,共2页 Chinese Journal of Cancer Prevention and Treatment
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同被引文献10

  • 1张忠德,殷敏智,奚政君,吴湘如.婴儿型纤维肉瘤的临床病理分析[J].临床与实验病理学杂志,2007,23(4):457-460. 被引量:5
  • 2Kampp J, Husain AN, et al. Pathologic quiz case: newborn with a subcutaneous facial mass. Arch Pathol Lab Med, 2003,127 (6) : e281-282.
  • 3Nonaka D, Sun CC. Congenital fibrosarcoma with metastasis in a fetus. Pediatric and Developmental Pathology, 2004,7 (2): 187-191.
  • 4Knezevich SR, Garnett MJ, Pysher TJ, et al. ETV6-NTRK3 gene fusions and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital and congenital fibrosarcoma. Cancer Res, 1998,58 (22) : 5046-5048.
  • 5Rubin BP, Chen CJ, MorganTW, et al. Congenitalmesoblastic nephsroma t (12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic andmolecular relationship to congenital (infantile) fibrosarcoma. Am J Pathol, 1998,153 (5):1451- 1458.
  • 6Russell H, Hicks M J, Bertuch AA, et al. Infantile fibrosarcoma: clinical and histologic responses to cytotoxic chemotherapy. Pediatric Blood Cancer, 2009,53 ( 1 ) : 23-27.
  • 7ErtUrk C, Yarmpapus R, Altay MA, et al. A giant congenital fibrosarcoma of the leg. J Pediatr Orthop B, 2010,19(4):348- 352.
  • 8彭格红,俞松,曹永政,陶文鸿.小儿皮肤皮下血管瘤的超声诊断:增生期或退化期的判断[J].中国医学影像技术,2007,23(11):1703-1705. 被引量:2
  • 9陈林莺,张声,施烯.婴儿型纤维肉瘤临床病理特征[J].中国现代医生,2010,48(28):76-78. 被引量:4
  • 10叶小剑,徐荣全,黄春燕,鄢磊.卵巢卵黄囊瘤的超声及临床、病理特征[J].中国医学影像技术,2017,33(7):1029-1032. 被引量:14

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