Angiomiolipoma hepático epitelioide: reporte de un caso

Ahumada, Oscar; Hepp, Juan; Gallegos, Marcela; Schiappacasse, Giancarlo

Publication:
Angiomiolipoma hepático epitelioide: reporte de un caso

dc.contributor.author	Ahumada, Oscar
dc.contributor.author	Hepp, Juan
dc.contributor.author	Gallegos, Marcela
dc.contributor.author	Schiappacasse, Giancarlo
dc.date.accessioned	2023-04-26T16:05:06Z
dc.date.available	2023-04-26T16:05:06Z
dc.date.issued	2022
dc.description.abstract	Angiomyolipomas (AML) are mesenchymal tumors belonging to the group of perivascular epithelioid cell tumors, which, rarely, can display a malignant behavior. They are composed of adipose tissue, vessels, and muscle tissue in different proportions, and constitute a differential diagnosis for other focal liver lesions. We report a 34-year-old woman in whom a focal hepatic lesion was discovered incidentally. The pathology report of an ultrasound guided biopsy informed an epithelioid angiomyolipoma, a rare variant of these lesions. During ten years of imaging follow, the size and features of the lesion has not changed. The patient rejected a surgical excision.
dc.description.version	Versión Publicada
dc.identifier.citation	AHUMADA ESPINOZA, Oscar et al . Angiomiolipoma hepático epitelioide: reporte de un caso. Rev. méd. Chile, Santiago , v. 150, n. 9, p. 1256-1259, sept. 2022 . Disponible en <http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872022000901256&lng=es&nrm=iso>. accedido en 26 abr. 2023. http://dx.doi.org/10.4067/S0034-98872022000901256
dc.identifier.doi	https://doi.org/10.4067/S0034-98872022000901256
dc.identifier.uri	https://repositorio.udd.cl/handle/11447/7398
dc.language.iso	es
dc.subject	Angiomyolipoma
dc.subject	Malignant mesenchymal tumor
dc.title	Angiomiolipoma hepático epitelioide: reporte de un caso
dc.type	Article
dcterms.accessRights	Acceso Abierto
dcterms.source	Revista médica de Chile
dspace.entity.type	Publication