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dc.contributor.authorButt FM.
dc.contributor.authorGuthua Symon W.
dc.contributor.authorChindia ML.
dc.contributor.authorRana F.
dc.contributor.authorOsundwa Tom M.
dc.date.accessioned2013-04-10T04:38:26Z
dc.date.available2013-04-10T04:38:26Z
dc.date.issued2009-12
dc.identifier.citationJ Craniomaxillofac Surg. 2009 Dec;37(8):434-7en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/15553
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/19836964
dc.description.abstractMelanotic neuroectodermal tumour of infancy (MNTI)/progonoma is a rare lesion affecting infants. Although it is slow growing and appears benign, it may have malignant potential. Evidently, surgery is the main stay of treatment and close follow-up is recommended for all cases. The literature shows that radiotherapy and chemotherapy may be indicated especially in cases where total surgical extirpation is equivocal. This article contributes three more cases of MNTI surgically managed at our institutionen
dc.language.isoenen
dc.titleEarly outcome of three cases of melanotic neuroectodermal tumour of infancyen
dc.typeArticleen
local.publisherDepartment of Oral and Maxillofacial Surgery, University of Nairobien


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