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Granular cell ameloblastoma of jaw: report of a case with an emphasis on its characterization

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Granular cell ameloblastoma of jaw: report of a case with an emphasis on its characterization

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dc.contributor.author Taneeru, Sravya es
dc.contributor.author Guttikonda, Venkateswara Rao es
dc.contributor.author Yeluri, Sivaranjani es
dc.contributor.author Madala, Jayakiran es
dc.date.accessioned 2014-05-22T09:38:00Z
dc.date.available 2014-05-22T09:38:00Z
dc.date.issued 2013 es
dc.identifier.citation Taneeru, Sravya ; Guttikonda, Venkateswara Rao ; Yeluri, Sivaranjani ; Madala, Jayakiran. Granular cell ameloblastoma of jaw: report of a case with an emphasis on its characterization. En: Journal of Clinical and Experimental Dentistry, 2013, Vol. 5, No. 3: 154-156 es
dc.identifier.uri http://hdl.handle.net/10550/35332
dc.description.abstract Ameloblastoma is a neoplasm of odontogenic epithelium, especially of enamel organ-type tissue that has not under gone differentiation to the point of hard tissue formation. It accounts for approximately 10% of all tumors originating from gnathic bones. It exhibits diverse microscopic patterns which occurs either singly or in combination with other patterns. Granular cell ameloblastoma is a rare condition, accounting for 3.5% of all ameloblastoma cases that shows marked transformation in the cytoplasm of tumor cells, which are usually stellate reticulum like cells. The transformed cells possess very coarse, granular, eosinophilic cytoplasm. The 'granular change' is thought to be due to a dysfunctional status of neoplastic cells, and the pathogenesis of this tumour seems to be age-related. Ultrastructural, histochemical, and immunohitochemical studies have revealed that cytoplasmic granularity is caused by overload; however the mechanism ivolved remains poorly understood. This article describes a case of granular cell variant of ameloblastoma affecting a 55-year old female en_US
dc.subject Odontología es
dc.subject Ciencias de la salud es
dc.title Granular cell ameloblastoma of jaw: report of a case with an emphasis on its characterization es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.type.hasVersion VoR es_ES

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