An uncommon association of cloacal malformation with Hirschsprung's Disease, congenital pouch colon and vaginal duplication Kloakal anomalinin Hirschsprung hastaliǧi, doǧumsal 'pouch' kolon ve vajinal duplikasyon ile seyreden nadir birlikteligi
Pediatrik Cerrahi Dergisi, cilt.15, sa.2, ss.81-84, 2001 (Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 15 Sayı: 2
- Basım Tarihi: 2001
- Dergi Adı: Pediatrik Cerrahi Dergisi
- Derginin Tarandığı İndeksler: Scopus
- Sayfa Sayıları: ss.81-84
- Anahtar Kelimeler: Cloacal malformation, Congenital pouch colon, Hirschsprung's disease, Vaginal duplication
- Sağlık Bilimleri Üniversitesi Adresli: Evet
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.