Surgical Approach to a Late-Diagnosed Coexistence of Megalourethra, Double Vagina and Uterus Didelphys Presenting with Total Urinary Incontinence in an Adolescent Girl Adolesan Kız Hastada Total Üriner Inkontinansla Seyreden Geç Tanı Almış Megaloüretra, Çift Vajina ve Uterus Didelfis Birlikteliğine Cerrahi Yaklaşım

Sezer B. T., YILMAZ M. U., PARLAK A., SAĞLAM S., Utangaç M. M., Balkan E., ...Daha Fazla

Cocuk Cerrahisi Dergisi, cilt.35, sa.3, ss.155-158, 2021 (Scopus) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 35 Sayı: 3
  • Basım Tarihi: 2021
  • Doi Numarası: 10.5222/jtaps.2021.59329
  • Dergi Adı: Cocuk Cerrahisi Dergisi
  • Derginin Tarandığı İndeksler: Scopus
  • Sayfa Sayıları: ss.155-158
  • Anahtar Kelimeler: adolescent, double vagina, megalourethra, urinary incontinence, uterus didelphys
  • Bursa Uludağ Üniversitesi Adresli: Evet

Özet

Mullerian duct anomalies can sometimes accompany urinary malformations and they can be diagnosed with different symptoms in late childhood. We aimed to present a thirteen year-old adolescent girl with megalourethra, double vagina and uterus didelphys who presented with total urinary incontinence. Her urogenital examination revealed a large orifice of megalourethra in the middle and two symmetric orifices of bifid vagina on both sides. An amorphous bladder with a large urethra was detected at cystoscopic examination. Urethral plication, resection of vaginal septum and reconstruction were performed. Congenital urological malformations associated with mullerian anomalies can be diagnosed with urinary symptoms in adolescence. Combined corrective surgery can be performed safely in a single session.