An adult situs ambiguous case with polysplenism

Basit Öğe Kaydı
dc.contributor.authorÖzkurt, H.
dc.contributor.authorNarin, B.
dc.contributor.authorArman, A.
dc.contributor.authorTasali, N.
dc.contributor.authorÇelik, L.
dc.date.accessioned2024-07-12T21:38:00Z
dc.date.available2024-07-12T21:38:00Z
dc.date.issued2006en_US
dc.department[Belirlenecek]en_US
dc.description.abstractSitus ambiguous is a rare anomaly that is characterised by abnormal arrangement of abdominal organs with congenital heart diseases. Patients rarely survive beyond first decade of life as this anomaly generally coexists with cyanotic heart diseases. The correct recogniation and characterisation of cases is important for planning surgical, radiologic and endoscoping interventions. In this case we present an incidentally diagnosed case with midline located liver, multiple spleens and stomach in the right upper quadrant, interruptured inferior vena cava with azygos continuation. The heart was left sided and there was no sign of congenital cardiac anomaly. Hereby we present this case as it was found incidentally at adult age and there was no accompanying congenital heart anomaly.en_US
dc.identifier.endpage203en_US
dc.identifier.issn1300-526X
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-33846867424en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage200en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12415/7022
dc.identifier.volume21en_US
dc.indekslendigikaynakScopus
dc.language.isotren_US
dc.relation.ispartofGoztepe Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.snmzKY04372
dc.subjectMultiple Spleensen_US
dc.subjectSitus Ambiguousen_US
dc.titleAn adult situs ambiguous case with polysplenismen_US
dc.typeArticle
dspace.entity.typePublication

Dosyalar

Koleksiyon

Scopus İndeksli Yayınlar Koleksiyonu