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Hypervascular neurofibromas in a case of neurofibromatosis type 1: a case report

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Hypervascular neurofibromas in a case of neurofibromatosis type 1: a case report

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dc.contributor.author Kashyap, Roopashri Rajesh es
dc.contributor.author Gogineni, Subhas Babu es
dc.date.accessioned 2016-06-24T12:25:42Z
dc.date.available 2016-06-24T12:25:42Z
dc.date.issued 2011 es
dc.identifier.citation Kashyap, Roopashri Rajesh ; Gogineni, Subhas Babu. Hypervascular neurofibromas in a case of neurofibromatosis type 1: a case report. En: Journal of Clinical and Experimental Dentistry, 2011, Vol. 3, No. 4-1: 356-359 es
dc.identifier.uri http://hdl.handle.net/10550/54214
dc.description.abstract Neurofibromatosis type 1 is one of the most frequently inherited diseases affecting 1:3500 newborn. The diagnosis of Neurofibromatosis type 1 is not dilemmatic because of typical clinical features. The key feature of Neurofibromatosis type 1, neurofibromas, are complex tumours arising from peripheral nerve sheaths. Neurofibromas may be focal growths or can extend along the length of a nerve, involving several fascicles and including nerve branches. Neurofibromas sometimes exhibit hypervascular characteristics. Few reports suggest the bleeding tendency observed in neurofibroma, although not common, occasionally causes a large amount of bleeding during surgical intervention. Hypervascular characteristics of these tumors may be a confusing factor for the diagnostician. This report describes the case of Neurofibromatosis type 1 presented with neurofibroma exhibiting hypervascular characteristics and emphasizes the importance of necessary investigations prior to sur gical procedures en_US
dc.subject Odontología es
dc.subject Ciencias de la salud es
dc.title Hypervascular neurofibromas in a case of neurofibromatosis type 1: a case report es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.type.hasVersion VoR es_ES

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