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dc.contributor.authorSani, PM
dc.contributor.authorTarzamni, MK
dc.contributor.authorAslanabadi, S
dc.contributor.authorSadat, ATE
dc.contributor.authorSani, AM
dc.contributor.authorNezami, N
dc.date.accessioned2018-08-26T08:16:43Z
dc.date.available2018-08-26T08:16:43Z
dc.date.issued2009
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51126
dc.description.abstractHepatic tumors are rare in children. About 50%-60% of these tumors are malignant. 65% of the liver malignancies are hepatoblastomas and most of the remainder are hepatocellular carcinomas. Yolk sac tumor (YST) is an extremely rare tumor of the liver. We report on a hepatic yolk sac tumor in a 15-month-old girl who presented with acute abdomen. She was diagnosed initially as intussusception. while ultrasonography and CT-scan indicated a liver mass. Finally, yolk sac tumor was diagnosed surgically and histopathologically.
dc.language.isoEnglish
dc.relation.ispartofIRANIAN JOURNAL OF RADIOLOGY
dc.subjectEndodermal Sinus Tumor
dc.subjectLiver
dc.subjectYolk Sac
dc.subjectUltrasonography
dc.subjectTomography
dc.subjectX-ray Computed
dc.titlePure Yolk Sac (Endodermal Sinus) Tumor of the Liver: A Case Report
dc.typeArticle
dc.citation.volume6
dc.citation.issue2
dc.citation.spage93
dc.citation.epage96
dc.citation.indexWeb of science
dc.citation.URLhttps://sites.kowsarpub.com/iranjradiol/articles/78929.html


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