Gallbladder paraganglioma

dc.contributor.authorEce, İlhan
dc.contributor.authorAlptekin, Hüsnü
dc.contributor.authorÇelik, Zeliha Esin
dc.contributor.authorŞahin, Mustafa
dc.date.accessioned2020-03-26T19:06:02Z
dc.date.available2020-03-26T19:06:02Z
dc.date.issued2015
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractGallbladder paraganglioma is a very rare tumor, and only a few cases have been reported. Most of these cases were asymptomatic and found incidentally during operation. Our case involved a 57-year-old female patient complaining of intermittent right upper quadrant pain. Preoperative imaging demonstrated a mass in the neck of the gallbladder. Laparoscopic cholecystectomy was performed, and a frozen section of the gallbladder demonstrated a benign mass. The postoperative pathologic examination reported gallbladder paraganglioma and chronic cholecystitis. Immunohistochemically, the chief cells and sustentacular cells showed diffuse positivity with vimentin, synaptophysin, and S-100.en_US
dc.identifier.doi10.5152/UCD.2014.2691en_US
dc.identifier.endpage246en_US
dc.identifier.issn2564-6850en_US
dc.identifier.issn2564-7032en_US
dc.identifier.issue4en_US
dc.identifier.pmid26668523en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage244en_US
dc.identifier.urihttps://dx.doi.org/10.5152/UCD.2014.2691
dc.identifier.urihttps://hdl.handle.net/20.500.12395/32187
dc.identifier.volume31en_US
dc.identifier.wosWOS:000370846700015en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherAVESen_US
dc.relation.ispartofTURKISH JOURNAL OF SURGERYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectGallbladderen_US
dc.subjectparagangliomaen_US
dc.subjectintra-abdominal massen_US
dc.titleGallbladder paragangliomaen_US
dc.typeArticleen_US

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