Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/5384
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dc.contributor.authorBernard, Aklen_US
dc.contributor.authorTeddy, Jabbouren_US
dc.contributor.authorAsad, Haydaren_US
dc.contributor.authorZarouhie, Bedoyanen_US
dc.contributor.authorFatme, Ghandouren_US
dc.contributor.authorMichel, Jabbouren_US
dc.date.accessioned2022-01-27T12:25:53Z-
dc.date.available2022-01-27T12:25:53Z-
dc.date.issued2021-
dc.identifier.issn00904295-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/5384-
dc.description.abstractOncocytic Papillary Renal Cell Carcinoma (OPRCC) is a rare variant of renal cell carcinoma with overlapping characteristics type 1 and 2 of papillary renal carcinoma. Based on the literature, OPRCC is predominantly present in adult males. OPRCC has a specific genetic affiliation with the Fumarate Hydratase gene requiring all patients diagnosed with OPRCC to undergo genetic testing. There isn't any agreement for the treatment of OPRCC due to the rarity of the disease; however, a radical nephrectomy poses as a possible modality. Therefore, we present the rare case of an 11-year-old female found to have OPRCC.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.titleOncocytic Papillary Renal Cell Carcinoma in an 11-year-old girlen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.urology.2021.04.009-
dc.identifier.pmid33891928-
dc.identifier.scopus2-s2.0-85107342808-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85107342808-
dc.contributor.affiliationFaculty of Medicineen_US
dc.description.volume156en_US
dc.date.catalogued2022-01-27-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.urology.2021.04.009en_US
dc.relation.ispartoftextUrologyen_US
dc.description.campusSGH campusen_US
Appears in Collections:Faculty of Medicine
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