dc.creatorParra-Medina, Rafael
dc.creatorGuio, José Ismael
dc.creatorLópez-Correa, Patricia
dc.date.accessioned2021-04-19T20:41:26Z
dc.date.accessioned2022-09-27T12:42:02Z
dc.date.available2021-04-19T20:41:26Z
dc.date.available2022-09-27T12:42:02Z
dc.date.created2021-04-19T20:41:26Z
dc.date.issued2016-03-17
dc.identifierhttp://dx.doi.org/10.1155/2016/8413987
dc.identifierhttps://repositorio.fucsalud.edu.co/handle/001/1441
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3596592
dc.description.abstractCastleman’s disease (CD) is a rare lymphoproliferative disorder of unknown etiology. It typically occurs in adulthood but it may also develop in childhood. Clinically, this disease may be classified as localized (unicentric) or systemic (multicentric). Six cases of breast CD have been described in the literature, and all have been reported in adults. Herein we describe the case of a 15-year-old female who presented with a slow-growing tumor in the right breast. The tumor was excised and histopathological examination demonstrated hyaline vascular variant CD. After two years of follow-up, the patient was asymptomatic without evidence of cervical or axillary lymphadenopathy.
dc.languageeng
dc.publisherHindawi
dc.publisherBudapest
dc.relationCase Reports in Pathology e-ISSN: 2090-679X año (2016)
dc.relationCase Reports in Pathology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAtribución 4.0 Internacional (CC BY 4.0)
dc.rightshttps://creativecommons.org/licenses/by/4.0/
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.sourcehttps://www.hindawi.com/journals/cripa/2016/8413987/
dc.titleLocalized Castleman’s Disease in the Breast in a Young Woman
dc.typeArtículo de revista


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