6
views
0
recommends
+1 Recommend
2 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      OHVIRA Syndrome with a Rare Presentation

      case-report

      Read this article at

      ScienceOpenPublisher
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          ABSTRACT

          Background

          Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome is a rare complex Mullerian anomaly with an incidence of 1:20,000. The commonest presentation is pain in the abdomen and progressive dysmenorrhea. Other rare symptoms could include vaginal discharge, fever, infertility, or acute abdomen.

          Case description

          A 15-year girl presented with acute retention of urine which required catheterization. She had attained menarche 8 months back. On evaluation, the ultrasonography report revealed the presence of uterine didelphys with right side pelvic collection and absent kidney on the same side of the collection. On magnetic resonance imaging (MRI), a right obstructed hemivagina was clearly seen along with other findings suggesting the OHVIRA syndrome. Laparoscopically, a bulge was seen just below the right uterine horn which caused the retention of urine. Septal resection was performed vaginally, following which her symptoms subsided.

          Clinical significance

          Suspect OHVIRA syndrome in adolescent girls when there is a renal anomaly with Mullerian defect. The patient can also present with acute retention of urine because of hematocolpos. Early detection and treatment will help to prevent complications of endometriosis and adverse fertility outcomes.

          How to cite this article

          Nandan N, Tanneru A, Rai P, et al. OHVIRA Syndrome with a Rare Presentation. J South Asian Feder Obst Gynae 2023;15(3):354–356.

          Related collections

          Most cited references6

          • Record: found
          • Abstract: not found
          • Article: not found

          Diagnosis, management, and outcome of obstructed hemivagina and ipsilateral renal agenesis (OHVIRA syndrome): Is there a correlation between MRI findings and outcome?

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Diagnostic challenges of hemihematocolpos and dysmenorrhea in adolescents: obstructed hemivagina, didelphys or bicornuate uterus and renal aplasia is a rare female genital malformation.

            To develop a clear diagnostic and therapeutic strategy for adolescents presenting with abdominal pain and vaginal tumor caused by congenital female genital anomalies, such as blind hemivagina and uterine anomalies, as the lack of the correct diagnosis of the underlying anatomical genitourinary malformation frequently leads to destructive surgical procedures.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Late presentation, MR imaging features and surgical treatment of Herlyn-Werner-Wunderlich syndrome (classification 2.2); a case report

              Background Herlyn-Werner-Wunderlich syndrome is a very rare congenital genitourinary anomaly characterized by uterus didelphys, blind hemivagina and ipsilateral renal agenesis. Case presentation Authors present a case of Herlyn-Werner-Wunderlich syndrome in a 19-year-old unmarried woman who presented with pelvic pain and pelvic mass. MR imaging revealed the typical features of didelphys uterus, obstructed right hemivagina and ipsilateral renal agenesis. The patient subsequently underwent surgery. Conclusions Herlyn-Werner-Wunderlich syndrome would be suspected in patients with unilateral absent kidney and pelvic mass. Ultrasonography and MR imaging can well depict the disease entity and surgery is the treatment of choice for obstructed hemivagina.
                Bookmark

                Author and article information

                Journal
                JSAFOG
                Journal of South Asian Federation of Obstetrics and Gynaecology
                JSAFOG
                Jaypee Brothers Medical Publishers
                0974-8938
                0975-1920
                May-June 2023
                : 15
                : 3
                : 354-356
                Affiliations
                [1–4 ]Department of Obstetrics and Gynaecology, KS Hegde Medical Academy, Mangaluru, Karnataka, India
                Author notes
                Neetha Nandan, Department of Obstetrics and Gynaecology, KS Hegde Medical Academy, Mangaluru, Karnataka, India, Phone: +91 9900001287, e-mail: nvyas@ 123456nitte.edu.in
                Article
                10.5005/jp-journals-10006-2244
                6e5ea0c9-34f6-419c-bca5-4a0290e941fe
                Copyright © 2023; The Author(s).

                © The Author(s). 2023 Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and non-commercial reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 25 December 2022
                : 27 February 2023
                : 31 July 2023
                Categories
                CASE REPORT
                Custom metadata
                jsafog-15-354.pdf

                Obstetrics & Gynecology
                Renal agenesis,Acute urinary retention,OHVIRA syndrome,Uterine didelphys

                Comments

                Comment on this article