Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.23/1254
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dc.contributor.authorPalma Rios, H-
dc.contributor.authorGoulart, A-
dc.contributor.authorLeão, P-
dc.date.accessioned2018-04-13T13:50:39Z-
dc.date.available2018-04-13T13:50:39Z-
dc.date.issued2018-
dc.identifier.citationCase Rep Surg. 2018 Jan 11;2018:6897372.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.23/1254-
dc.description.abstractPseudomyxoma peritonei (PMP) and extragastrointestinal stromal tumors (E-GISTs) are both rare entities. Most of the time, PMP is associated with an appendiceal tumor. An ovarian mucinous tumor can mimic appendiceal metastases. E-GIST is a mesenchymal tumor that can arise from the omentum, retroperitoneum, mesentery, or pleura. We present a case of an 87-year-old woman with mucinous carcinomatosis and acute intestinal occlusion submitted to an emergency laparotomy. She has found to have a borderline mucinous tumor of the ovary from the intestinal type with several lesions of pseudomyxoma peritonei and an E-GIST from the epiploons retrocavity (intermediated risk). In the literature, no relation was found between these two rare tumors. E-GIST was an incidental finding in the context of a mucinous carcinomatosis.pt_PT
dc.language.isoengpt_PT
dc.rightsopenAccesspt_PT
dc.subjectAdenocarcinoma Mucinosopt_PT
dc.titleMucinous Carcinomatosis: A Rare Association between an Ovarian Tumor and an E-GISTpt_PT
dc.typearticlept_PT
dc.peerreviewedyespt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
degois.publication.firstPage6897372pt_PT
degois.publication.lastPage4pt_PT
degois.publication.volume2018pt_PT
dc.identifier.doi10.1155/2018/6897372pt_PT
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