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
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.