Correlation of MRI Findings in Optic Pathway Glioma with the Presence of Neurofibromatosis
DOI:
https://doi.org/10.21276/9y504080Keywords:
Glioma, Optic Pathway, NeurofibromatosisAbstract
Background: Optic nerve glioma (also known as optic pathway glioma) is the most common primary neoplasm of the optic nerve. The tumor can arise anywhere along the optic pathway from behind the globe to the occipital cortex. Optic pathway gliomas (OPGs) are associated with high rate of visual morbidity and mortality. Studies have shown no specific clinical histologic or neuro imaging features to differentiate aggressive from non-aggressive OPGs. Purpose: The biological behaviour of optic pathway glioma is unpredictable and it is not clear if specific anatomical patterns may be of use in prognosis of the OPGs. The prognosis is reportedly better in OPGs associated with neurofibromatosis (NF). The purpose of the study was to compare the MRI findings between patients with NF, with those without NF and to determine prognostic imaging signs if any. Material and Methods - MRI studies of 41 patients with OPG (21 with NF and 20 without NF) were reviewed at presentation and at follow up. Statistical bivariate analysis was used to compare the size and extension of tumor between patients with and those without NF. Results: Orbital component of the optic nerve was most commonly involved in patients with NF (65%) with optic chiasma being the most common site of involvement (90%) in the non NF group. Extension beyond the optic pathway at diagnosis was more frequent in the non-NF group. In patients with NF, the morphological appearance of the optic nerve was preserved with the tumor being of limited size as compared to the patients in the non-NF group. Statistically significant correlation between MRI features and growth pattern of glioma was absent. Conclusion: As per our study we found that more than half the NF patient’s tumor size remained stable in contrast to less than 5% of the non-NF group. Although no statistical correlation was found between MRI imaging and the biological behaviour of the tumor, we can infer that NF OPG is a separate entity from non-NF OPG with different prognostic features requiring a customised approach as per the type.
Downloads
References
Alshail E, Rutka JE, Becher LE, Hoffman JH. Optic chiasmatic-hypothalamic glioma. Brain pathol 1997;7:799-806.
Barkovich JA. Paediatric Neuroimaging. Philadelphia: Lippincott Williams & Wilkins; 1997:5v07-509.
Dutton JJ Gliomas of the anterior visual pathway,surv ophthalmol 1994;38;427-452
McCulloughDC Epstein F,optic pathway tumor,a review with proposal of clinical staging.cancer 1985;56 1789-1791
Wisoff JH,Management of optic pathwaytumors of childhood. Neurosurgclin north Am 1992;3,791-802
Packers RJ ,Bilaniuk LT,Cohen BH,et al Intracranial visual pathway gliomas in children with neurofibromatosis,neurofibromatosis 1998,127;212-222
Listernick R,Darling C,Greenwald M,Strauss L,Charrow J, optic pathway tumors in children ;the effect of neurofibromatosis type 1 on clinical manifestations and natural history.J Pediatr 1995;127 718-722
Deliganis AV,Geyer JR, Berger MS, Prognostic significance of type 1 neurofibromatosis in childhood optic glioma neurosurgery 1996;38;1114-1119
Hoffman HJ,Humphreys RP,Drake JM,et al,optic pathway/hypothalamic gliomas a dilemma in managament pediatr neurosurgery 1993;19;186-195
Lund AM,SkovbyF,optic glioma in children with neurofibromatosis type 1Eur J pediatr 1991;150;835-838
Sutton LN,Visual pathway gliomas of childhood contemp neurosurg 1994;16;1-6
Medlock MD ,Madsen JR,Barnes PD et al.optic chiasm astrocytomas of childhood. Pediatr neurosurg 1997;27,121-128
Jann AJ, Grundy R, Cnaan A et al, optic pathway and hypothalamic /chiasmatic gliomas in children younger than age 5,years with a 6 year
follow up cancer 1995;75;1051-1059
Listernick R, charrow J,Greenwald M,Mets M,Natural history of optic pathway tumors in children with neurofibromatosis
Listernick R, Louis DN,Packer RJ,Gutman DH,optic pathway gliomas in children with neurofibromatosis 1,consensus statement from the NF1 optic pathway glioma task force,Ann Neurol 1997: 41 143-149.
Downloads
Published
Issue
Section
License
Copyright (c) 2024 International Archives of BioMedical and Clinical Research
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Authors are required to sign and submit the completed “Copyright transfer Form” upon acceptance of publication of the paper. This is determined by a publishing agreement between the author and International Archives of Biomedical and Clinical Research. These rights might include the right to publish, communicate and distribute online. Author(s) retain the copyright of their work. International Archives of Biomedical and Clinical Research supports the need for authors to share, disseminate and maximize the impact of their research.