Beatrice Randi
University of Bologna
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Journal of Pediatric Surgery | 2010
Mario Lima; Giovanni Ruggeri; Beatrice Randi; Marcello Dòmini; Tommaso Gargano; Enrico La Pergola; Giulio Gregori
BACKGROUND/PURPOSE The absence of vagina is rare in the pediatric population. It can occur as a result of congenital malformations such as an aplasia of mullerian ducts (46,XX Mayer-Rokitansky-Küster-Hauser syndrome) or a complete androgen insensitivity syndrome (46,XY testicular feminizing syndrome). Intersex patients, who underwent reassessment of a female sex, need a genital reconstruction toward a feminine phenotype. Patients with congenital adrenogenital syndrome with high urogenital sinus could have a severe hypoplastic vagina. In all these cases, a vaginal replacement is required. We reviewed our experience of vaginal replacement using a sigmoid conduit. METHODS In 34 years, we evaluated 47 patients. The observation period was from 1 to 34 years (mean: 12 years). The preoperative diagnosis was Mayer-Rokitansky-Küster-Hauser syndrome in 17 cases, androgen insensitivity syndrome in 24 cases, adrenogenital syndrome with high urogenital sinus in 5 and 1 patient was affected by penile agenesis. Forty-six patients were treated with vaginal reconstruction by interposition of sigmoid colon. Only in 1 case we performed a vaginal construction with an ileal loop: in this case, the sigmoid colon was extremely dilated by a chronic constipation secondary to a high anorectal malformation corrected at birth. RESULTS The outcome for 47 patients is excellent: 18 are sexually active and 4 are married. Only 1 patient with adrenogenital syndrome died of endocrine problems. Complications occurred in 17 cases: in 1 patient a necrosis of the replaced vagina occurred, thus requiring vaginal exeresis; now she is waiting for a second operation. Another patient had an abdominal abscess, which was surgically treated. In 12 cases a second procedure was required: 6 had stenotic new-vaginal introitus, 4 had new-vaginal prolapse, and 2 had intestinal obstruction. CONCLUSIONS We believe that the preferable technique for vaginal replacement is the use of intestinal conduit. The sigmoid colon is the best intestinal tract to be used owing to its size, location and preserved blood supply. Our experience leads us to believe that the sigmoid segment is the segment of choice, although we consider ileal loop as a good alternative when the sigmoid colon is not available.
Archive | 2012
Mario Lima; Marcello Dòmini; Giulio Gregori; Beatrice Randi
Il pneumotorace (Pnx) e una raccolta d’aria nel cavo pleurico che determina uno schiacciamento del polmone e il conseguente collasso [1]. Questo collasso polmonare puo essere parziale o totale, arrivando, nelle forme ipertese, a determinare anche uno sbandieramento del mediastino verso l’emitorace del lato opposto.
Pediatric Surgery International | 2012
Giovanni Ruggeri; Tommaso Gargano; Claudio Antonellini; Veronica Carlini; Beatrice Randi; Francesca Destro; Mario Lima
La Pediatria Medica e Chirurgica | 2012
Mario Lima; F. Molinaro; Giovanni Ruggeri; Tommaso Gargano; Beatrice Randi
European Journal of Pediatric Surgery | 2010
Mario Lima; Beatrice Randi; Tommaso Gargano; Tani G; A. Pession; Giulio Gregori
JEMIS Journal of Endoscopic and Minimally Invasive Surgery in Newborn, Children and Adolescent | 2014
Mirella Mogiatti; Giovanni Ruggeri; Tommaso Gargano; Beatrice Randi; Mario Lima
Surgical Endoscopy and Other Interventional Techniques | 2012
Mario Lima; Giovanni Ruggeri; Francesco Molinaro; Tommaso Gargano; Giulio Gregori; Beatrice Randi
JEMIS Journal of Endoscopic and Minimally Invasive Surgery in Newborn, Children and Adolescent | 2014
Ciro Andolfi; Beatrice Randi; Giovanni Ruggeri; Mario Lima
JEMIS Journal of Endoscopic and Minimally Invasive Surgery in Newborn, Children and Adolescent | 2014
Giovanni Ruggeri; Beatrice Randi; Tommaso Gargano; Michele Libri; Michela Maffi; Mario Lima
ESPES 2nd annual scientific meeting | 2013
Giovanni Ruggeri; Tommaso Gargano; Michele Libri; Beatrice Randi; Michela Maffi; Mario Lima