期刊文献+

骶骨外脊柱少见部位脊索瘤的临床病理特征分析 被引量:1

Clinicopathological characteristics of mobile spinal chordoma
在线阅读 下载PDF
导出
摘要 目的探讨发生于脊柱少见部位的脊索瘤的临床特点及诊断和治疗方法。方法收集2001年12月至2013年10月发生于颈、胸、腰椎的6例脊索瘤患者的临床资料,包括临床表现、影像学和病理学特点以及接受外科治疗的情况。结果 6例脊索瘤的发生部位:腰椎3例,颈椎2例,胸椎1例。6例均接受手术治疗,术后随访时间平均38.7个月(12~45个月)。术后复发2例,均为囊内切除边界。1例全身多发转移,术后5个月死亡。病理组织学检查均表现为脊索瘤经典型形态:肿瘤细胞片状分布或呈条索状和散在分布于丰富的黏液性间质中,肿瘤细胞主要由含空泡的液滴样细胞和嗜酸性星形细胞构成。结论颈、胸、腰椎脊索瘤罕见,临床症状多不典型,容易漏诊或误诊,需结合影像学和病理学表现诊断,囊内切除后复发率高。 Objective To investigate the clinicopathological characteristics and the methods of diagnosis and treatment of chor- doma sites occurred in rare mobile spine. Methods The clinical data of six cases of spinal chordoma occurred in cervical, thoracic and lumbar from December 2001 to December 2013 in our center were analyzed, which including clinical manifestations, radiological features, pathological diagnosis, and surgical treatment. Results There were three cases in lumbar vertebrae, two cases in cervical vertebrae and one case in thoracic vertebrae. All cases received surgical treatment. The average postoperative follow-up time was 38.7(12-45) months. Recurrence occurred in two cases which had intraeapsular resection margin. One patient died of multiple metastases postoperative. Pathol- ogy showed classic chordoma morphology. Tumor cells showed a patchy distribution or cords and scattered in mucinous abundant intersti- tial. The tumor was composed of droplets like cells containing vacuole and eosinophilie astrocytes. Conclusion The cervical, thoracic and lumbar spinal chordomas are rare. The clinical symptoms are not typical and easily missed or misdiagnosed. The diagnosis should com- bine with radiological and pathological characteristic. The recurrence rate is high after intracapsular excision.
出处 《临床肿瘤学杂志》 CAS 2015年第7期646-650,共5页 Chinese Clinical Oncology
基金 国家自然科学基金资助项目(61372179)
关键词 脊索瘤 脊柱 临床特点 诊断与治疗 Chordoma Spine Clinical characteristic Diagnosis and treatment
作者简介 通讯作者,E-mail:niuxiaohui@263.net
  • 相关文献

参考文献15

  • 1Casali PG, Stacchiotti S, Sangaili C, et al. Chordoma[ J]. CurrOpin Oncol, 2007, 19:367-370.
  • 2Topsakal C, Bulut S,Erol FS,et al. Chordoma of the thoracicspine-case report[ J]. Neurol Med Chir(Tokyo),2002, 42(4):175-180.
  • 3Rena O,Davoli F,Allegra G, et al. Giant chordoma of the upperthoracic spine with mediastinal involvement : a surgical challenge[J]. Asian Spine J, 2014, 8(3):353-356.
  • 4Guillonnet A, Bengolea L, Funes J, et al. Cervical chordomawith moderate bone impairment in a child [ J ]. Diagnostic and In-terventional Imaging, 2012, 93( 11) : 903-906.
  • 5Choi GH, Yang MS, Yoon do H, et al. Pediatric cervical chordo-ma :report of two cases and a review of the current literature[ J].Childs Nerv Syst, 2010, 26(6) :835-840.
  • 6Boriani S, Bandiera S, Biagini R, et al. Chordoma of the mobilespine: fifty years of experience[ J]. Spine,2006, 31 (4) :493-503.
  • 7Miyazawa N, Ishigame K, Kato S, et al. Thoracic chordoma:re-view and role of FDG-PET[ J]. J Neurosurg Sci, 2008,52(4);117-121.
  • 8Inigo C,Juan A, Raul F, et al. Chondroid Chordoma in an Atyp-ical Location [ J ] . Arch Bronconeumol, 2013, 49( 11):491-493.
  • 9Heffelfinger MJ, Dahlin DC, MacCarty CS, et al. Chordomas andcartilaginous tumors at the skull base [ J ]. Cancer, 1973,32(2):410-420.
  • 10Crapanzano JP, Ali SZ, Ginsberg MS, et al. Chordoma: a cyto-logic study with histologic and radiologic correlation[ J]. Cancer,2001, 93(1):40-51.

二级参考文献20

  • 1张俊廷,王亮,吴震,贾桂军,张力伟.颅底脊索瘤患者生存因素分析[J].中华医学杂志,2007,87(23):1607-1610. 被引量:7
  • 2McMaster M L,Goldstein A M,Bromley C M,et al.Chordoma:incidence and survival patterns in the United States,1973-1995[J].Cancer Causes Control,2001,12(1):1-11.
  • 3Romeo S,Hogendoorn P C.Brachyury and chordoma:the chondroid-chordoid dilemma resolved[J].J Pathol,2006,209(2):143-6.
  • 4Yamaguchi T,Suzuki S,Ishiiwa H,et al.Benign notochordal cell tumors a comparative histological study of benign notochordal cell tumors,classic chordomas,and notochordal vestiges of fetal intervertebral discs[J].Am J Surg Pathol,2004,28(6):756-61.
  • 5Heffelfinger M J,Dahlin D C,Maccarty C S,Beabout J W.Chordomas and cartilaginous tumours at the skull base[J].Cancer,1973,32(2):410-20.
  • 6Crapanzano J P,Ali S Z,Ginsberg M S.Chordoma a cytologic study with histologic and radiologic correlation[J].Cancer,2001,93(1):40-51.
  • 7Bisceglia M,D Angelo V A,Guglielmi G,et al.Defifferentialed chordoma of the thoracic spine with rhabdomyosarcomatous differentiation.Report of a case and review of the literation[J].Ann Diagn Pathol,2007,11(4):262-73.
  • 8Garcia R A,Inwards C Y,Unni K K.Benign bone tumors-recent developments[J].Semin Diagn Pathol,2011,28(1):73-85.
  • 9Suster S,Moran C A.Chordomas of the mediastinum:clinicopathologic,immunohistochemical,and ultrastructural study of six cases presenting as posterior mediastinal masses[J].Hum Pathol,1995,26(12):1354-62.
  • 10Barry J J,Jian B J,Sughrue M E,et al.The next step:innovative molecular targeted therapies for treatment of intracranial chordoma patients[J].Neurosurgery,2011,68(1):231-40.

共引文献10

同被引文献12

引证文献1

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