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Letter| Volume 32, ISSUE 3, P345, June 2019

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Two Successful Pregnancies after a Previous Cloacal Repair

  • Colin A. Walsh
    Correspondence
    Address correspondence to: Colin A. Walsh, MB, BCh, BAO, MRCPI, MRCOG, FRANZCOG, CCT-MFM (UK), PhD, Department of Maternal-Fetal Medicine, North Shore Private Hospital, 460 Pacific Highway, Suite G6, St Leonards, Sydney, New South Wales, Australia
    Affiliations
    Department of Maternal-Fetal Medicine, North Shore Private Hospital, Sydney, New South Wales, Australia
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Published:February 04, 2019DOI:https://doi.org/10.1016/j.jpag.2019.01.008
      I read with much interest the recent review by Vilanova-Sanchez et al regarding the obstetrical outcomes of women with previous cloacal repairs.
      • Vilanova-Sanchez A.
      • McCracken K.
      • Halleran D.R.
      • et al.
      Obstetrical outcomes in adult patients born with complex anorectal malformations and cloacal anomalies: a literature review.
      I recently cared for a woman whose case adds nicely to this excellent review. The patient, a 30-year-old physician, was born with a 2.5-cm cloaca with an associated didelphys uterus and 2 hemivaginas. Definitive surgical repair was undertaken at 19 months of age by Dr Alberto Pena, one of the surgical pioneers, who was visiting Sydney at that time.
      • Pena A.
      • Levitt M.A.
      • Hong A.
      • et al.
      Surgical management of cloacal malformations: a review of 339 patients.
      The patient underwent a posterior sagittal anorectoplasty including excision of the vaginal septum. Subsequently, in childhood, a bilateral ureteric reimplantation was performed for vesicoureteral reflux.
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      References

        • Vilanova-Sanchez A.
        • McCracken K.
        • Halleran D.R.
        • et al.
        Obstetrical outcomes in adult patients born with complex anorectal malformations and cloacal anomalies: a literature review.
        J Pediatr Adolesc Gynecol. 2019; 32: 7
        • Pena A.
        • Levitt M.A.
        • Hong A.
        • et al.
        Surgical management of cloacal malformations: a review of 339 patients.
        J Pediatr Surg. 2004; 39: 470

      Linked Article

      • Obstetrical Outcomes in Adult Patients Born with Complex Anorectal Malformations and Cloacal Anomalies: A Literature Review
        Journal of Pediatric and Adolescent GynecologyVol. 32Issue 1
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          Patients born with complex anorectal malformations often have associated Müllerian anomalies, which might affect fertility and obstetrical outcomes. Other vertebral-anorectal-tracheoesophageal-renal-limb associations, such as renal or cardiac anomalies, could also affect pregnancy intention, fertility rates, and recommendations about mode of delivery or obstetrical outcomes. Associated conditions present at birth, like hydrocolpos, could also potentially affect fertility. Depending on the complexity of the anomaly, primary reconstruction might include vaginoplasty, vaginal interposition, perineal body reconstruction, and extensive pelvic dissection.
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