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dc.contributor.authorMacin, G.
dc.contributor.authorHekimoglu, K.
dc.contributor.authorUner, H.
dc.contributor.authorTarhan, C.
dc.date.accessioned2019-12-26T07:54:06Z
dc.date.available2019-12-26T07:54:06Z
dc.date.issued2014
dc.identifier.issn1780-2393
dc.identifier.urihttps://pdfs.semanticscholar.org/8e56/5d24c47969c59f5d232b6e7d020ee440a326.pdf?_ga=2.111229121.497193966.1577346743-640473402.1577346743
dc.identifier.urihttp://hdl.handle.net/11727/4556
dc.description.abstractLymphangiomas are rare congenital benign tumors arising from the lymphatic system mostly encountered in the neck and axillary regions of pediatric patients. Pancreatic cystic lymphangiomas very rarely occur in adults. Radio-logically, the lesion may mimic pancreatic carcinoma and should be considered in the differential diagnosis of any patient found to have an abdominal cystic mass. In this article, we present a 50-year-old man who presented with pain in the upper abdomen, nausea, and abdominal swelling. On computed tomography (CT) and magnetic resonance (MR) imaging, a gross septated cystic lesion was detected in the upper abdomen which extended from the pancreatic corpus to the left liver lobe. The patient underwent complete resection of tumor Pathology revealed a cystic lymphangioma.en_US
dc.language.isoengen_US
dc.relation.isversionof0.5334/jbr-btr.26en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectLymphangiomaen_US
dc.titlePANCREATIC CYSTIC LYMPHANGIOMA: DIAGNOSTIC APPROACH WITH MDCT AND MR IMAGINGen_US
dc.typearticleen_US
dc.relation.journalJBR-BTRen_US
dc.identifier.volume97en_US
dc.identifier.issue2en_US
dc.identifier.startpage97en_US
dc.identifier.endpage99en_US
dc.identifier.wos000350837600008


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