Please use this identifier to cite or link to this item: http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/12411
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dc.contributor.authorKumanan, T.-
dc.contributor.authorMathangi, N.-
dc.contributor.authorSuganthan, N.-
dc.contributor.authorBrammah, R.T.-
dc.date.accessioned2026-03-27T04:27:31Z-
dc.date.available2026-03-27T04:27:31Z-
dc.date.issued2026-
dc.identifier.urihttp://repo.lib.jfn.ac.lk/ujrr/handle/123456789/12411-
dc.description.abstractPlexiform neurofibromas are benign nerve sheath tumours commonly associated with neurofibromatosis type 1 (NF1). Plexiform neurofibromas of the scalp is a rare finding. Plexiform neurofibroma in the occipital region is even rarer. The commonest skull manifestations in neurofibromatosis involve the orbit, with very few reports about occipital defects. Magnetic resonance imaging (MRI) is the preferred modality to identify the lesion. It is usually managed by surgical excision, but recurrence has also been reported even after thorough removal. We present a case of a 52-year-old man with plexiform neurofibroma in the occipital region with skull erosions which is an extremely rare findingen_US
dc.language.isoenen_US
dc.publisherSri Lanka College of Internal Medicineen_US
dc.subjectPlexiform neurofibromaen_US
dc.subjectBone erosionsen_US
dc.subjectNeurofibromatosis type 1 (NF1)en_US
dc.subjectOccipital plexiform neurofibromaen_US
dc.titleA rare case of occipital plexiform neurofibroma with skull erosions in neurofibromatosis type 1en_US
dc.typeCase reporten_US
Appears in Collections:Medicine



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