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Urachal Tumor: A Case Report of an Extremely Rare Carcinoma

dc.contributor.authorGarcia, J.
dc.contributor.authorSampaio, R.
dc.contributor.authorPeixoto, C.
dc.date.accessioned2017-08-29T15:23:04Z
dc.date.available2017-08-29T15:23:04Z
dc.date.issued2017
dc.description.abstractThe urachus is a tubular structure that connects the bladder to the allantois in the embryonic development, involuting after the third trimester. The urachus carcinoma is an extremely rare tumor that accounts for <1% of all bladder cancers. We report a case of a 46-year-old woman, with no past medical history, complaining of hematuria with 6-month duration and a physical exam and an abdominal computed topographic scan revealing an exophytic mass of 6.8 cm longer axis that grew depending on the anterior bladder wall, invading the anterior abdominal wall. Cystoscopy detected mucosal erosion. The biopsy showed structures of adenocarcinoma of enteric type. The surgical specimen showed urachus adenocarcinoma of enteric type with stage IVA in the Sheldon system and stage III in the Mayo system. This case has a 3-year follow-up without disease recurrence.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationCase Rep Pathol. 2017;2017:1942595pt_PT
dc.identifier.doi10.1155/2017/1942595pt_PT
dc.identifier.issn2090-679X
dc.identifier.issn2090-6781
dc.identifier.urihttp://hdl.handle.net/10400.16/2172
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherHindawi Publishing Corporationpt_PT
dc.relation.publisherversionhttps://www.hindawi.com/journals/cripa/2017/1942595/pt_PT
dc.titleUrachal Tumor: A Case Report of an Extremely Rare Carcinomapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceUnited States of Americapt_PT
oaire.citation.startPage1942595pt_PT
oaire.citation.titleCase Reports in Pathologypt_PT
oaire.citation.volume2017pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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