Literature DB >> 6818504

Optic glioma. Long-term follow-up of 85 histopathologically verified cases.

J A Rush, B R Younge, R J Campbell, C S MacCarty.   

Abstract

Eighty-five cases of histologically verified gliomas of the optic nerve or chiasm were studied retrospectively. Patient survival was analyzed according to location of tumor, treatment received, presence of neurofibromatosis, and degree of histologic anaplasia. Thirty-three patients had optic nerve tumors, and 52 had tumors involving the chiasm. Follow-up ranged from 6 days to 43.7 years. Of the 33 patients with optic nerve tumors, 28 (85%) survived a mean duration of 17 years, and survival was significantly associated with completeness of surgical excision. Twenty-three of the 52 patients (44%) with chiasmal tumors survived a mean duration of 19 years. Survival among patients with chiasmal tumors was unrelated to therapy received and was affected adversely by concomitant involvement of adjacent brain structures. The presence of neurofibromatosis conferred a protective benefit to patients with chiasmal tumors. No other significant factors could be statistically identified to influence the prognosis of patients with optic gliomas.

Entities:  

Mesh:

Year:  1982        PMID: 6818504

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  20 in total

1.  Optic glioma of childhood: clinical, histopathological, and histochemical observations.

Authors:  S Bilgiç; A Erbengi; B Tinaztepe; B Onol
Journal:  Br J Ophthalmol       Date:  1989-10       Impact factor: 4.638

2.  Childhood chiasmal gliomas: update on the fate of patients in the 1969 San Francisco Study.

Authors:  R K Imes; W F Hoyt
Journal:  Br J Ophthalmol       Date:  1986-03       Impact factor: 4.638

3.  Visual outcomes in pediatric optic pathway glioma after conformal radiation therapy.

Authors:  Richard M Awdeh; Erin N Kiehna; Richard D Drewry; Natalie C Kerr; Barrett G Haik; Shengjie Wu; Xiaoping Xiong; Thomas E Merchant
Journal:  Int J Radiat Oncol Biol Phys       Date:  2012-05-18       Impact factor: 7.038

Review 4.  Clinical and genetic patterns of neurofibromatosis 1 and 2.

Authors:  N K Ragge
Journal:  Br J Ophthalmol       Date:  1993-10       Impact factor: 4.638

Review 5.  Ophthalmological manifestations in VHL and NF 1: pathological and diagnostic implications.

Authors:  Klaus-Martin Kreusel
Journal:  Fam Cancer       Date:  2005       Impact factor: 2.375

6.  Optic nerve glioma and the management of optic nerve tumours in the young.

Authors:  J E Wright; A A McNab; W I McDonald
Journal:  Br J Ophthalmol       Date:  1989-12       Impact factor: 4.638

7.  Assessment of chemotherapeutic response in children with proptosis due to optic nerve glioma.

Authors:  Roberto Jose Diaz; Suzanne Laughlin; Gary Nicolin; J Raymond Buncic; Eric Bouffet; Ute Bartels
Journal:  Childs Nerv Syst       Date:  2007-12-22       Impact factor: 1.475

8.  Optic chiasm glioma associated with inappropriate secretion of antidiuretic hormone, cerebral ischemia, nonobstructive hydrocephalus and chronic ascites following ventriculoperitoneal shunting.

Authors:  T T Tang; H T Whelan; G A Meyer; D R Strother; E L Blank; B M Camitta; R A Franciosi
Journal:  Childs Nerv Syst       Date:  1991-12       Impact factor: 1.475

Review 9.  An integrated approach to the treatment of chiasmatic-hypothalamic gliomas.

Authors:  M Garvey; R J Packer
Journal:  J Neurooncol       Date:  1996 May-Jun       Impact factor: 4.130

10.  Analysis of 20 primarily surgically treated chiasmatic/hypothalamic pilocytic astrocytomas.

Authors:  J M Valdueza; F Lohmann; O Dammann; C Hagel; B Eckert; N Freckmann
Journal:  Acta Neurochir (Wien)       Date:  1994       Impact factor: 2.216

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