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Pseudomyxoma peritonei: a clinical case of this poorly understood condition

dc.contributor.authorOliveira, AM
dc.contributor.authorRodrigues, C
dc.contributor.authorBorges, A
dc.contributor.authorMartins, A
dc.contributor.authorSantos, S
dc.contributor.authorPires, F
dc.contributor.authorAraújo, JM
dc.contributor.authorDeus, JR
dc.date.accessioned2014-04-24T11:25:56Z
dc.date.available2014-04-24T11:25:56Z
dc.date.issued2014
dc.description.abstractBACKGROUND: Pseudomyxoma peritonei is an uncommon condition with an estimated incidence of one to two per million (worldwide) per year. It is characterized by the peritoneal deposition of mucinous tumors, most commonly of the appendix, and occasionally from the ovary, coupled by mucinous ascites. CASE PRESENTATION: We report the case of a 76-year-old woman who presented with increased abdominal girth and dyspnea for 2 weeks. She was diagnosed as a case of pseudomyxoma peritonei. She was submitted to right oophorectomy, omentectomy, and pseudomyxoma debulking. The histology was compatible with a mucinous tumor of colorectal/appendicular origin. Chemotherapy was not administered because of her functional status. Two years and 8 months later, she refers with postprandial fullness and has moderate ascites.por
dc.identifier.citationInt J Gen Med. 2014 Mar 3;7:137-41por
dc.identifier.issn1178-7074
dc.identifier.urihttp://hdl.handle.net/10400.10/1148
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherDove Medical Presspor
dc.relation.publisherversionhttp://www.dovepress.com/articles.php?article_id=15991&l=QunbpSKVHKBJWd4LXQ62Zk85332546por
dc.subjectpseudomyxoma peritoneipor
dc.titlePseudomyxoma peritonei: a clinical case of this poorly understood conditionpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceAuckland, N.Zpor
oaire.citation.endPage141por
oaire.citation.startPage137por
oaire.citation.titleInternational Journal of General Medicinepor
oaire.citation.volume7por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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