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Angiomyolipoma of the upper lip : case report and review of the literature

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Angiomyolipoma of the upper lip : case report and review of the literature

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dc.contributor.author Silva, Andréia Aparecida da es
dc.contributor.author Carlos, Román es
dc.contributor.author Contreras Vidaurre, Elisa es
dc.contributor.author Almeida, Oslei Paes de es
dc.contributor.author Lopes, Márcio Ajudarte es
dc.contributor.author Vargas, Pablo Agustín es
dc.date.accessioned 2017-11-23T07:47:45Z
dc.date.available 2017-11-23T07:47:45Z
dc.date.issued 2007 es
dc.identifier.citation Silva, Andréia Aparecida da ; Carlos, Román ; Contreras Vidaurre, Elisa ; Almeida, Oslei Paes de ; Lopes, Márcio Ajudarte ; Vargas, Pablo Agustín. Angiomyolipoma of the upper lip : case report and review of the literature. En: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, 12 2 2007: 4- es
dc.identifier.uri http://hdl.handle.net/10550/63264
dc.description.abstract Angiomyolipoma (AML) is a hamartomatous growth that usually affects the kidney. One third of patients with AML present with manifestations of tuberous sclerosis. Oral AML is rare with only 6 cases reported in the English-language literature. In the present case, AML was located in the upper lip of a 43 year-old woman. Clinically, it presented as a firm nodule, well circumscribed and measuring 1x2 cm. It was surgically excised. Histopathological analysis showed a lesion composed of an admixture of smooth muscle cells, blood vessels, and adipose tissue. The immunohistochemical study revealed positivity for vimentin, smooth muscle actin, pan specific muscle actin and desmin. CD68, CD34 and mast cell antibodies showed focal immunoreactivity. S100 protein, Ki-67, and HMB-45 were negative. Based on these histological and immunohistochemical features the diagnosis was of oral AML. No recurrence was observed after 2 years of follow-up. es
dc.title Angiomyolipoma of the upper lip : case report and review of the literature es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.identifier.doi es
dc.type.hasVersion VoR es_ES

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