Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/5963
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dc.contributor.authorEl Asmar, Antoineen_US
dc.contributor.authorEl Rassi, Ziaden_US
dc.date.accessioned2022-08-02T09:10:44Z-
dc.date.available2022-08-02T09:10:44Z-
dc.date.issued2016-
dc.identifier.issn2210-2612-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/5963-
dc.description.abstractHepatoblastoma is the most common primary liver tumor for children under 5 years of age. It usually presents as an abdominal mass, symptomatic only when large enough to cause mass effect on nearby organs. Symptoms such as early satiety, anorexia, abdominal pain or weight loss are the most common. Diagnosis depends on imaging studies, AFP levels and percutaneous biopsy. Treatment modality is usually surgical with neoadjuvant chemotherapy.en_US
dc.language.isoengen_US
dc.publisherNational Library of Medicineen_US
dc.subjectChemotherapyen_US
dc.subjectHepatoblastoma case reportsen_US
dc.subjectLong term survivalen_US
dc.subjectSurgical resectionen_US
dc.subjectTotal remissionen_US
dc.titleHepatoblastoma in childhood, long term survival achieved: 2 case reports and literature reviewen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.ijscr.2016.02.019-
dc.identifier.pmid26942331-
dc.identifier.scopus2-s2.0-84963570032-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84963570032-
dc.contributor.affiliationFaculty of Medicineen_US
dc.description.volume21en_US
dc.description.startpage55en_US
dc.description.endpage58en_US
dc.date.catalogued2022-08-02-
dc.description.statusPublisheden_US
dc.identifier.openURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802225/en_US
dc.relation.ispartoftextInternational Journal of Surgery Case Reportsen_US
dc.description.campusSGH campusen_US
Appears in Collections:Faculty of Medicine
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