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先天性纤维肉瘤一例报道并文献复习 被引量：1

Congenital fibrosarcoma:Report of one case and review of the literatures
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摘要 先天性纤维肉瘤是发生于5岁以下个体的一类少见的软组织恶性肿瘤。本文报道1例左侧头颈部巨大先天性纤维肉瘤患者,通过对该病例的临床表现、影像学特点、治疗及病理结果的报道,结合相关文献进行讨论、分析,以了解该病的诊疗现状。 Congenital fibrosarcoma is a rare soft tissue malignant tumor that usually presents m the children under the age of 5. This paper reports a case of huge congenital fibrosarcoma of left hand and neck and reviews the relevant literatures regarding to the clinical, radiographic and pathological features to cognize the current diagnostic and therapeutic situation.
作者 郁鑫 赵小朋 范松 潘朝斌
机构地区 中山大学孙逸仙纪念医院口腔颌面外科
出处 《中华口腔医学研究杂志（电子版）》 CAS 2013年第2期57-58,共2页 Chinese Journal of Stomatological Research(Electronic Edition)
基金 广东省科技计划(2011B031800124 2012B031800252)
关键词 先天性纤维肉瘤 Congenital fibrosarcoma
分类号 R739.91 [医药卫生—肿瘤]
  • 相关文献

参考文献9

  • 1Kampp J, Husain AN, et al. Pathologic quiz case: newborn with a subcutaneous facial mass. Arch Pathol Lab Med, 2003,127 (6) : e281-282.
  • 2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
  • 3段守兴,李建宏,王广欢,张镟,钟军,祁艳卫,蒋学武.小儿先天性纤维肉瘤一例报道并文献复习[J].中华肿瘤防治杂志,2011,18(23):1887-1888. 被引量：2
  • 4Nonaka D, Sun CC. Congenital fibrosarcoma with metastasis in a fetus. Pediatric and Developmental Pathology, 2004,7 (2): 187-191.
  • 5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
  • 6Knezevich 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.
  • 7Rubin 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.
  • 8Russell 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.
  • 9ErtUrk C, Yarmpapus R, Altay MA, et al. A giant congenital fibrosarcoma of the leg. J Pediatr Orthop B, 2010,19(4):348- 352.

二级参考文献35

  • 1李懿堂,杨红,徐钢,曹文安,李光容.先天性纤维肉瘤6例病理分析[J].临床与实验病理学杂志,1993,9(1):11-13. 被引量：1
  • 2Kampp J, Husain AN, et al. Pathologic Quiz Case:Newborn with a subcutaneous facial mass[J]. Arch Pathol Lab Med,2003,127(6):281-282.
  • 3Stout AP. Fibrosarcoma in infants and children[J]. Cancer, 1962,15: 1028-1040.
  • 4Chung EB, Enzinger FM. Infantile fibrosarcoma[J]. Cancer, 1976,38 (2) : 729-739.
  • 5Marino-Enrtquez A,Li P, Samuelson J, Rossi MR, et al. Congenital fibrosarcoma with a novel complex 3-way translocation t (12; 15; 19) and unusual histologic features[J]. Hum Pathol, 2008,39(12) : 1844-1848.
  • 6Buceoliero AM, Castiglione F, Degl'Innocenti DR, et al. Congenital/Infantile fibrosarcoma of the colon : morphologic,immunohistochemical, molecular,and ultrastructural features of a relatively rare tumor in an extraordinary localization[J]. J Pediatr Hematol Oncol, 2008,30(10) : 723-737.
  • 7Yan AC, Chamlin SL, Liang MG, et al. Congenital infantile fibrosarcoma: a masquerader of ulcerated hemangioma[J]. Pediatr Dermatol, 2006,23 (4) : 330-334.
  • 8Katz P,Colbert R,Drolet B. Unilateral mosaic cutaneous vascular lesions, enchondroma,multiple soft tissue chondromas and congenital fibrosarcoma-a variant of Maffucci syndrome? [J]. Pediatr Dermatol,2008,25 (2): 205 -209.
  • 9Dahl I,Save-Soderberg J,Angervall L. Fibrosarcoma in early infancy[J]. Pathol Eur, 1973,8(3) : 193-209.
  • 10Sheng WQ, Hisaoka M, Okamoto S, et al. Congenital-Infantile fibrosarcoma:a clinicopathologic study of 10 cases and molecular detection of the ETV6-NTRK3 fusion transcr/pts using paraffin-embedded tissues[J].Am J Clin Pathol, 2001,115 (3) : 348-355.

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中华口腔医学研究杂志（电子版）
2013年 第2期

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