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Urachal carcinoma: imaging findings

dc.contributor.authorMonteiro, Vanessa
dc.contributor.authorCunha, Teresa Margarida
dc.date.accessioned2016-10-07T15:15:31Z
dc.date.available2016-10-07T15:15:31Z
dc.date.issued2012
dc.date.updated2016-07-23T14:09:58Z
dc.description.abstractUrachal carcinoma is a rare neoplasm, which accounts for only 0.5–2% of bladder malignancies, and arises from a remnant of the fetal genitourinary tract. A 46-year-old woman presented with a history of pelvic pain and frequent daytime urination. Ultrasound (US), computed tomography (CT), and magnetic resonance (MR) demonstrated a supravesical heterogeneous mass with calcifications. The patient underwent a partial cystectomy with en-bloc resection of the mass and histopathological examination revealed the diagnosis of urachal adenocarcinoma. Urachal carcinomas are usually associated with poor prognosis and early diagnosis is fundamental. CT and MR are useful to correctly diagnose and preoperatively staging.pt_PT
dc.identifier2047-9816en_US
dc.identifier.citationVanessa Monteiro; Teresa Margarida Cunha. Urachal carcinoma: imaging findings, Acta Radiologica Short Reports, 1, 1, 4-4, 2012.pt_PT
dc.identifier.doi10.1258/arsr.2011.110018pt_PT
dc.identifier.issn2047-9816
dc.identifier.urihttp://hdl.handle.net/10400.26/15054
dc.language.isoengpt_PT
dc.subjectUrinarypt_PT
dc.subjectCTpt_PT
dc.subjectMR imagingpt_PT
dc.subjectUltrasoundpt_PT
dc.subjectBladderpt_PT
dc.subjectNeoplasms – primarypt_PT
dc.titleUrachal carcinoma: imaging findingspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage3pt_PT
oaire.citation.issue4pt_PT
oaire.citation.startPage1pt_PT
oaire.citation.titleActa Radiologica Short Reportspt_PT
oaire.citation.volume1pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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