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Hamartoma mioide, serie de casos y revisión de la literatura

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dc.contributor.author Uchida, Marcela
dc.contributor.author Altamirano, Aleen
dc.contributor.author Horvath, Eleonora
dc.contributor.author Pinochet, Miguel
dc.contributor.author Galleguillos, Maria
dc.contributor.author Wenzel, Heriberto
dc.contributor.author Gallegos, Marcela
dc.date.accessioned 2017-08-10T19:20:40Z
dc.date.available 2017-08-10T19:20:40Z
dc.date.issued 2016
dc.identifier.citation Rev Chil Rad.2016; 22(4):184-188
dc.identifier.uri http://hdl.handle.net/11447/1557
dc.identifier.uri http://dx.doi.org/10.1016/j.rchira.2016.11.009
dc.description.abstract Myoid hamartoma is a rare entity, and was first described by Davies and Riddell in 1973. It is pathologically defined as the mixture of fatty glandular tissue and fibrous connective tissue, associated with a widespread focus of fusiform muscle cells. Six cases of HM diagnosed in seven patients are presented, with emphasis on imaging findings and characteristics of their respective core biopsies. The importance of biopsy in these lesions is required to differentiate malignant diseases. There is no need for excisional biopsy, because this is not associated with high-risk lesions or carcinomas.
dc.format.extent 5
dc.language.iso spa
dc.publisher Sociedad Chilena de Radiologia
dc.subject Breast
dc.subject Hamartoma
dc.subject Myoid hamartoma
dc.subject Muscle hamartoma
dc.title Hamartoma mioide, serie de casos y revisión de la literatura
dc.title.alternative Myoid hamartoma: A case series and literature review
dc.type Artículo


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