Orbitotemporal Neurofibromatosis: Case Report

Plexiform neurofibromas occur in about 60% of neurofibromatosis type 1(NF-1) patients and can lead to severe morbidity by disfigurement or compression of vital structures. Moreover, these tumors can undergo malignant transformation. Both focal and localized bone abnormalities are part of the phenoty...

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Main Authors: Mahalakshmi Balasubramanyam, Goutham Cugati, Bipasha Mukherjee
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Case Reports in Ophthalmological Medicine
Online Access:http://dx.doi.org/10.1155/2012/498186
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author Mahalakshmi Balasubramanyam
Goutham Cugati
Bipasha Mukherjee
author_facet Mahalakshmi Balasubramanyam
Goutham Cugati
Bipasha Mukherjee
author_sort Mahalakshmi Balasubramanyam
collection DOAJ
description Plexiform neurofibromas occur in about 60% of neurofibromatosis type 1(NF-1) patients and can lead to severe morbidity by disfigurement or compression of vital structures. Moreover, these tumors can undergo malignant transformation. Both focal and localized bone abnormalities are part of the phenotypic expression of NF-1. We report a rare case of severe cranioorbital plexiform neurofibromatosis in a young male and discuss the classification, clinical features, and various treatment options of orbit-temporal neurofibromatosis type 1.
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institution Kabale University
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publishDate 2012-01-01
publisher Wiley
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series Case Reports in Ophthalmological Medicine
spelling doaj-art-bfd54e9bf018450fbfceec099422a5e32025-02-03T05:52:33ZengWileyCase Reports in Ophthalmological Medicine2090-67222090-67302012-01-01201210.1155/2012/498186498186Orbitotemporal Neurofibromatosis: Case ReportMahalakshmi Balasubramanyam0Goutham Cugati1Bipasha Mukherjee2Sankara Nethralaya, 18 College Road, Chennai 600034, IndiaALNC, Post Graduate Institute of Neurological Surgery, VHS Hospital and Research Centre, TTTI Post, Taramani, Chennai 600113, IndiaDepartment of Orbit, Oculoplasty & Trauma, Sankara Nethralaya, 18 College Road, Chenna 600006, IndiaPlexiform neurofibromas occur in about 60% of neurofibromatosis type 1(NF-1) patients and can lead to severe morbidity by disfigurement or compression of vital structures. Moreover, these tumors can undergo malignant transformation. Both focal and localized bone abnormalities are part of the phenotypic expression of NF-1. We report a rare case of severe cranioorbital plexiform neurofibromatosis in a young male and discuss the classification, clinical features, and various treatment options of orbit-temporal neurofibromatosis type 1.http://dx.doi.org/10.1155/2012/498186
spellingShingle Mahalakshmi Balasubramanyam
Goutham Cugati
Bipasha Mukherjee
Orbitotemporal Neurofibromatosis: Case Report
Case Reports in Ophthalmological Medicine
title Orbitotemporal Neurofibromatosis: Case Report
title_full Orbitotemporal Neurofibromatosis: Case Report
title_fullStr Orbitotemporal Neurofibromatosis: Case Report
title_full_unstemmed Orbitotemporal Neurofibromatosis: Case Report
title_short Orbitotemporal Neurofibromatosis: Case Report
title_sort orbitotemporal neurofibromatosis case report
url http://dx.doi.org/10.1155/2012/498186
work_keys_str_mv AT mahalakshmibalasubramanyam orbitotemporalneurofibromatosiscasereport
AT gouthamcugati orbitotemporalneurofibromatosiscasereport
AT bipashamukherjee orbitotemporalneurofibromatosiscasereport