期刊文献+

松果体实质肿瘤25例临床病理观察 被引量:2

Pineal parenchymal tumors:a clinicopathologic analysis of 25 cases
下载PDF
导出
摘要 目的 观察松果体实质肿瘤(pineal parenchymal tumors,PPTs)的临床病理学特征、免疫表型,探讨其诊断、鉴别诊断、治疗和预后。方法 回顾性分析25例PPTs的临床病理资料、免疫表型等,结合文献分析其临床病理学特征。结果 25例PPTs中,男性14例,女性11例,年龄1.3~63岁,中位年龄42岁。其中,13例为松果体细胞瘤(52%),4例为中分化松果体实质肿瘤(pineal parenchymal tumors of intermediate differentiation,PPTID)(16%),8例为松果体母细胞瘤(32%)。结论 PPTs以松果体细胞瘤最常见,多见于成人,其次为松果体母细胞瘤,多发生于婴幼儿及青少年,PPTID最罕见。PPTs确诊依赖病理检查和免疫表型,电镜检查对确诊有一定帮助。肿块完整切除是PPTs适宜的治疗方法。 Purpose To investigate the clinicopathologic and immunohistochemical features of pineal parenchymal tumors (PPTs), and to discuss the diagnosis, differential diagnosis, treatment and prognosis of the tumor. Methods Histopathological characteristics and immunohistochemical results of 25 cases of PPTs were retrospectively studied and the relevant literatures were reviewed. Result 14 patients were male and 11 patients were female, which aged from 2 - 63 with a median of 42 years old. 13 eases were pineocytomas (52%) , 4 cases were pineal parenchymal tumors of intermediate differentiation (PPTID) ( 16% ) , 8 cases were pincoblastomas ( 32% ). Conchlsion The most common type of PPTs is pineocytoma, which occurs in middle age, followed by pineoblastoma, which occurs primarily in the first two decades of life, and PPTID is rare. The diagnosis of PPTs rely on the histopathology. Immunohistochemical and electronmicroscope results are definite value for diagnosis. The suitable treatment is gross total resection of the tumor.
出处 《临床与实验病理学杂志》 CAS CSCD 北大核心 2014年第5期506-510,514,共6页 Chinese Journal of Clinical and Experimental Pathology
关键词 松果体实质细胞肿瘤 临床病理学 免疫组织化学 治疗 pineal parenchymal tumors clinicopathologie immunobistochemistry treatment
  • 相关文献

参考文献22

  • 1Dahiya S, Perry A. Pineal tumors[J]. Adv Anat Pathol, 2010,17 (6) :419 -27. 被引量:1
  • 2Louis D N, Ohgaki H, Wiestler O D, et al. WHO classification of tumours of the central nervous system[ M]. 4th ed. Lyon: IARC Press, 2007 : 122 - 7. 被引量:1
  • 3Sato K, Kubota T. Pathology of pineal parenchymal tumors[J]. Prog Neurol Surg, 2009,23 : 12 - 25. 被引量:1
  • 4Jouvet A, Saint-Pierre G, Fauchon F, et al. Pineal parenchymal tumors: a correlation of histological, features with prognosis in 66 cases [ J]. Brain Pathol, 2000,10 ( 1 ) :49 - 60. 被引量:1
  • 5McLendon R E, Rosenblum M K, Bigner D D, et al. Russell & Rubinstein' s pathology of tumors of the nervous system[ M]. 7th ed. London: Hodder Arnold, 2006:413 - 25. 被引量:1
  • 6Berns S, Pearl G. Review of pineal anlage tumor with divergent histology [ J ]. Arch Pathol Lab Med, 2006,130 (8) : 1233 - 5. 被引量:1
  • 7Fevre-Montange M, Champier J, Szathmari A, et al. Microarray analysis reveals differential gene expression patterns in tumors of the pineal region [ J ]. J Neuropathol Exp Neurol, 2006,65 ( 7 ) : 675 - 84. 被引量:1
  • 8Han S J, Clark A J, Ivan M E, et al. Pathology of pineal paren- chymal tumors[ J ]. Neurosurg Clin N Am, 2011,22 ( 3 ) : 335 - 40. 被引量:1
  • 9Rickert C H, Simon R, Bergmann M, et al. Comparative genomic hybridization in pineal parenchymal tumors [ J ]. Genes Chromo- somes Cancer, 2001,30( 1 ) :99 - 104. 被引量:1
  • 10Li G, Mitra S, Karamchandani J, et al. Pineal parenchymal tumor of intermediate differentiation: clinicopathological report and anal- ysis of epidermal growth factor receptor variant III expression 3]. Neurosurgery, 2010, 66 ( 5 ) : 963 - 8. 被引量:1

二级参考文献10

  • 1Sasaki A,Horiguchi K,Nakazato Y.Pineal parenchymal tumor of intermediate differentiation with cytologic pleo-morphism[J].Neuropathology,2006,26(3):212-217. 被引量:1
  • 2Pusztaszeri M,Pica A,Janzer R.Pineal parenchymal tu-mors of intermediate differentiation in adults:case report and literature review[J].Neuropathology,2006,26(2):153-157. 被引量:1
  • 3Jouvet A,Fèvre-Moutange,Besancon R,et al.Structural and ultrastructural characteristics of human pineal gland,and pineal parenchuymal tumors[J].Acta Neuropathol,1994,88(4):334-348. 被引量:1
  • 4Mena H,Rushing EJ,Ribas JL,et al.Tumors of pineal parenchymal cells:a correlation of histological features,in-cluding nucleolar organizer regions,with survival in35cases[J].Hum Pathol,1995,26(1):20-30. 被引量:1
  • 5Schild SE,Scheithauer BW,Schomberg PJ,et al.Pineal parenchymal tuomrs.Clinical,pathologic,and therapeutic aspects[J].Cancer,1993,72(3):870-880. 被引量:1
  • 6Schild SE,Scheithauer BW,Haddock MG,et al.Histologi-cally confirmed pineal tumors and other germ cell tumors of the brain[J].Cancer,1996,78(2):2564-2571. 被引量:1
  • 7Fauchon F,Jouvet A,Paquis P,et al.Parenchymal pineal tumors:a clinicopathological study of76cases[J].Int J Radiat Oncol Biol Phys,2000,46(4):959-968. 被引量:1
  • 8Flecher CDM主编.回允中译.肿瘤组织病理学诊断[M].第3版.北京:北京大学医学出版社,2009.1699. 被引量:1
  • 9滕梁红,卢德宏,徐庆中.浅谈WHO(2007)中枢神经系统肿瘤分类中新增的肿瘤类型[J].诊断病理学杂志,2007,14(6):406-410. 被引量:6
  • 10蔡颖,印洪林,陆珍凤,周航波,周晓军.松果体细胞瘤8例临床病理特征[J].临床与实验病理学杂志,2009,25(5):473-476. 被引量:3

共引文献2

同被引文献10

引证文献2

二级引证文献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