dc.contributor.author | Butt FM. | |
dc.contributor.author | Guthua Symon W. | |
dc.contributor.author | Chindia ML. | |
dc.contributor.author | Rana F. | |
dc.contributor.author | Osundwa Tom M. | |
dc.date.accessioned | 2013-04-10T04:38:26Z | |
dc.date.available | 2013-04-10T04:38:26Z | |
dc.date.issued | 2009-12 | |
dc.identifier.citation | J Craniomaxillofac Surg. 2009 Dec;37(8):434-7 | en |
dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/15553 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/pubmed/19836964 | |
dc.description.abstract | Melanotic 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 institution | en |
dc.language.iso | en | en |
dc.title | Early outcome of three cases of melanotic neuroectodermal tumour of infancy | en |
dc.type | Article | en |
local.publisher | Department of Oral and Maxillofacial Surgery, University of Nairobi | en |