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成人视路胶质瘤的诊断与显微外科治疗 被引量:2

Diagnosis and treatment of optic pathway glioma in adult
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摘要 目的报道8例成人视路胶质瘤,并结合文献讨论了成人视路胶质瘤的临床特点、影像学改变及显微手术方法。方法8例患者均行额下入路手术治疗,6例术中镜下全切除肿瘤、1例部分切除、1例仅行活检,术后此2例患者接受了放射治疗(失随访)。余6名患者随访8个月 ̄3a,平均1.26a。结果术后6例患者视力改善、2例视力无变化。无死亡病例。病理:5例为胶质瘤I~Ⅱ级,3例为胶质瘤Ⅱ、Ⅲ级。结论成人视神经胶质瘤最早的临床表现为视力下降,结合MRI的影像学改变,术前应可做出高度倾向性的诊断。成人视路胶质瘤多累及视交叉,仅发生于一侧视神经者少见。显微手术有可能全切除肿瘤,肿瘤全切除患者的生存期较文献报告延长。无法全切除者术后应辅以放疗。 [Objective] To study their imageology and clinical characteristic as well as surgical strategy of 8 cases in adult optic pathway glioma. [Methods] The operations were performed in all of 8 cases. 6 of 8 optic pathway gliomas w ere total removed, and one glioma was part removed, another glioma only biopsy. Radiotherapy were performed in 2 patients which their tumor was not total remove d. [Results] Acuity of vision improved post-operation in 6 patients,no change in 2 patients; Pathology: 5 cases with glioma I~Ⅱgrade and 3 cases with Ⅱ~ Ⅲ. [Conclusions] Visual disorder is the most original clinical symptoms in ad ult optic pathway glioma and the tumor often involve the chiasm. Total remove th e tumor is possible when micro-operation. Radiotherapy should be performed when tumor residue.
出处 《中国现代医学杂志》 CAS CSCD 北大核心 2005年第10期1526-1528,共3页 China Journal of Modern Medicine
关键词 视路 胶质瘤 显微手术 放疗 pathway glioma operation radiotherapy
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参考文献6

  • 1KHAFAGA Y, HASSOUNAH M, KANDIL A, et al. Optic gliomas: a retrospective analysis of 50 cases[J]. Int J Radiat Oncol Biol Phys, 2003, 56(3): 807-812.
  • 2LUO SQ. Intracranial Tumors in Children[M]. People's Medical Publishing House, Beijing. 1992: 175-184. Chinese
  • 3CZYZYK E, JOZWIAK S, ROSZKOWSKI M, SCHWARTZ PA.Optic pathway gliomas in children with and without neurofibromatosis[J]. J Child Neurol, 2003, 18(7): 471-478.
  • 4ALVORD EC, LOFTON S: Gliomas of the optic nerve or chiasm:out-come by patients age, tumor site, and treatment[J]. J Neurosurg, 1988, 68: 85-98.
  • 5FLICKINGER JC, TORRES C, DEUTSCH M. Management of low-grade gliomas of the optic nerve and chiasm [J]. Cancer,1988, 61: 635-642.
  • 6ASTRUP J. Natural history and clinical management of optic pathway glioma[J]. Br J Neurosurg, 2003, 17(4): 327-335.

同被引文献8

  • 1Nicolin G, Parkin P, Mabbott D, et al. Natural history and outcome of optic pathway gliomas in children [J]. Pediatr Blood Cancer, 2009, 53(7): 1231-1237.
  • 2Khafaga Y, Hassounah M, Kandil A, et al. Optic gliomas: a retrospective analysis of 50 cases [J]. Int J Radiat Oncol Biol Phys, 2003, 56(3): 807-812.
  • 3Segal L, Darvish-Zargar M, Dilenge ME, et al. Optic pathway gliomas in patients with neurofibromatosis type 1: follow-up of 44 patients [J]. J AAPOS, 2010, 14 (2): 155- 158.
  • 4Astrup J. Natural history and clinical management of optic pathway glioma [J]. Br J Neurosurg, 2003, 17(4): 327-335.
  • 5Watson, GA, Kadota RP, Wisoff, JH. Muhidiseiplinary management of pediatric low-grade gliomas [J]. Semin Radiat Oneol, 2001, 11(2): 152-162.
  • 6Halperin EC, Constine LS, Tarbell N J, et al. Pediatric radiation oncology [M]. Philadelphia: Lippincott, Williams & Wilkins, 1999. 47-50.
  • 7Silva MM, Goldman S, Keating G, et al. Optic pathway hypothalamic gliomas in children under three years of age: The role of chemotherapy [J]. Pediatr Neurosurg, 2000, 33 (3): 151-158.
  • 8Chikai K, Ohnishi A, Kato T, et al. Clinicopathological features of pilomyxoid astrocytoma of the optic pathway [J]. Acta Neuropathol, 2004, 108(2): 109-114.

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