Polisplenizm ile karakterize erişkin situs ambiguous olgusu

Küçük Resim Yok

Tarih

2006

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Galenos Yayınevi

Erişim Hakkı

info:eu-repo/semantics/openAccess

Araştırma projeleri

Organizasyon Birimleri

Dergi sayısı

Özet

Situs 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.

Açıklama

Anahtar Kelimeler

Multiple spleens, situs ambiguous

Kaynak

Göztepe Tıp Dergisi

WoS Q Değeri

Scopus Q Değeri

Cilt

21

Sayı

4

Künye

Özkurt, H., Narin, B., Akman, A. vd. (2006). Polisplenizm ile karakterize erişkin situs ambiguous olgusu / An adult situs ambiguous case with polysplenism. Göztepe Tıp Dergisi, Galenos Yayınevi. 21(4), s. 200-203.