Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report

R Angotti; F Molinaro; A L Bulotta; F Ferrara; M Sica; E Bindi; M Messina

doi:10.21699/jns.v5i3.326

Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report

J Neonatal Surg. 2016 Jul 3;5(3):32. doi: 10.21699/jns.v5i3.326. eCollection 2016 Jul-Sep.

Authors

R Angotti¹, F Molinaro¹, A L Bulotta¹, F Ferrara¹, M Sica¹, E Bindi¹, M Messina¹

Affiliation

¹ Division of Pediatric Surgery, Department of Medical, Surgical and Neurological Sciences, University of Siena, Viale Bracci 53100 Siena, Italy.

Abstract

More than 50% of infants with esophageal atresia have associated anomalies. We present a case report of a 46XX neonate with long-gap esophageal atresia and tracheoesophageal fistula (EA/TEF), anorectal malformation, bowel duplication and vaginal agenesis. This is an unusual association of abnormalities which had not yet described in literature.

Keywords: Anorectal malformation; Bowel duplication; Esophageal atresia; Mullerian anomalies.

Publication types

Case Reports