[A rare case of bladder exstrophy with a completely malformed complex in a girl].

Report of the observation of a female newborn presenting a complex malformative set: distal anorectal malformation without fistula; bladder exstrophy without epispadias, with cutaneous bridge; congenital urethrovaginal fistula; malformative sexual ambiguity with bulky genital tubercle, whole urethra, urethral meatus on the apex of the genital tubercle, associated with a mid labial genital joint and a high genital orifice; unilateral multicystic kidney; vertebral abnormalities with supernumerary thoracolumbar vertebrae; no karyotype abnormalities and no familial pathological history; no endocrine abnormalities. The therapeutic multistage program permitted a good reconstruction of the different lesion, particularly with bladder functioning witch in hope a good continence with two years of follow-up. No similar case is reviewed in the literature.
AuthorsJ F Dyon, E Sabatier, H Dodat, P Andrini, P Baudain, J P Alibeu
JournalChirurgie pédiatrique (Chir Pediatr) Vol. 31 Issue 6 Pg. 354-6 ( 1990) ISSN: 0180-5738 [Print] FRANCE
Vernacular TitleUn cas inhabituel d'extrophie vésicale avec ensemble malformatif complexe chez une fille.
PMID2091849 (Publication Type: Case Reports, English Abstract, Journal Article)
  • Abnormalities, Multiple
  • Anal Canal (abnormalities)
  • Bladder Exstrophy
  • Female
  • Fistula (congenital)
  • Humans
  • Infant
  • Infant, Newborn
  • Rectum (abnormalities)
  • Urethral Diseases (congenital)
  • Urogenital Abnormalities
  • Vaginal Diseases (congenital)

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