An uncommon association of cloacal malformation with Hirschsprung's Disease, congenital pouch colon and vaginal duplication
[ X ]
Tarih
2001
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Cloacal malformations are characterized by a single opening that connects the urinary tract, the internal genitalia and the intestinal tract via a urogenital sinus. We describe the first reported case of a cloacal malformation consisting of congenital pouch colon associated with Hirschsprung's Disease and vaginal duplication in a 13 year-old girl. We also discussed the method of surgical treatment performed in this girl. To plan reconstruction for an individual case with cloaca, the surgeon should be acquainted with associated anomalies and a wide range of anatomy that may be present.
Açıklama
Anahtar Kelimeler
Cloacal Malformation, Congenital Pouch Colon, Hirschsprung's Disease, Vaginal Duplication
Kaynak
Pediatrik Cerrahi Dergisi
WoS Q Değeri
Scopus Q Değeri
N/A
Cilt
15
Sayı
2
