A rare presentation of plexiform neurofibroma

We report on a rare case of a child with persistent right upper lid eversion with conjunctival prolapse since birth that failed various attempts in repositioning the right superior fornix at other centre. He was found to have a right supero-temporal orbital mass above the prolapsed area. Computerize...

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Main Authors: Poh, Khay Wei, Syed Osman SIH
Format: Article
Language:English
Published: Pusat Perubatan Universiti Kebangsaan Malaysia 2018
Online Access:http://journalarticle.ukm.my/12556/
http://journalarticle.ukm.my/12556/1/8._poh__syed.pdf
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author Poh, Khay Wei
Syed Osman SIH,
author_facet Poh, Khay Wei
Syed Osman SIH,
author_sort Poh, Khay Wei
building UKM Institutional Repository
collection Online Access
description We report on a rare case of a child with persistent right upper lid eversion with conjunctival prolapse since birth that failed various attempts in repositioning the right superior fornix at other centre. He was found to have a right supero-temporal orbital mass above the prolapsed area. Computerized tomography (CT) scan of orbit confirmed a right lacrimal gland tumour with thinning of the right lesser wing of sphenoid. An excision biopsy of the tumour via anterior orbitotomy and eyelid reconstruction were performed. Histopathology report reviewed plexiform neurofibroma of the lacrimal gland. Further physical examination confirmed presence of multiple café-au-lait spots. He was diagnosed as Neurofibromatosis Type 1.
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spelling oai:generic.eprints.org:125562019-02-14T21:33:41Z http://journalarticle.ukm.my/12556/ A rare presentation of plexiform neurofibroma Poh, Khay Wei Syed Osman SIH, We report on a rare case of a child with persistent right upper lid eversion with conjunctival prolapse since birth that failed various attempts in repositioning the right superior fornix at other centre. He was found to have a right supero-temporal orbital mass above the prolapsed area. Computerized tomography (CT) scan of orbit confirmed a right lacrimal gland tumour with thinning of the right lesser wing of sphenoid. An excision biopsy of the tumour via anterior orbitotomy and eyelid reconstruction were performed. Histopathology report reviewed plexiform neurofibroma of the lacrimal gland. Further physical examination confirmed presence of multiple café-au-lait spots. He was diagnosed as Neurofibromatosis Type 1. Pusat Perubatan Universiti Kebangsaan Malaysia 2018 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/12556/1/8._poh__syed.pdf Poh, Khay Wei and Syed Osman SIH, (2018) A rare presentation of plexiform neurofibroma. Journal of Surgical Academia, 8 (1). pp. 39-42. ISSN 2231-7481 http://jsurgacad.com/toc/8/1
spellingShingle Poh, Khay Wei
Syed Osman SIH,
A rare presentation of plexiform neurofibroma
title A rare presentation of plexiform neurofibroma
title_full A rare presentation of plexiform neurofibroma
title_fullStr A rare presentation of plexiform neurofibroma
title_full_unstemmed A rare presentation of plexiform neurofibroma
title_short A rare presentation of plexiform neurofibroma
title_sort rare presentation of plexiform neurofibroma
url http://journalarticle.ukm.my/12556/
http://journalarticle.ukm.my/12556/
http://journalarticle.ukm.my/12556/1/8._poh__syed.pdf