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Hematocolpos in women with uterus didelphys, imperforate hemivagina and ipsilateral renal agenesis: A case report and review of the literature
INTRODUCTION AND IMPORTANCE: Hematocolpos can be part of a rare syndrome OHVIRA or Herlyn-Werner-Wunderlich syndrome that requires special management (Brousse et al., n.d. [1]). The diagnosis can be delayed, yet an early diagnosis is important in order to elaborate an adequate strategy management an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189987/ http://dx.doi.org/10.1016/j.ijscr.2022.107277 |
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author | M'hamdi, Oumaima Boujida, Sarah Bensghir, Ibtissam Baidada, Aziz Lakhdar, Amina Kharbach, Aicha |
author_facet | M'hamdi, Oumaima Boujida, Sarah Bensghir, Ibtissam Baidada, Aziz Lakhdar, Amina Kharbach, Aicha |
author_sort | M'hamdi, Oumaima |
collection | PubMed |
description | INTRODUCTION AND IMPORTANCE: Hematocolpos can be part of a rare syndrome OHVIRA or Herlyn-Werner-Wunderlich syndrome that requires special management (Brousse et al., n.d. [1]). The diagnosis can be delayed, yet an early diagnosis is important in order to elaborate an adequate strategy management and prevent the patient from complications. CASE PRESENTATION: We report the case of a 14-year-old girl suffering from an hematocolpos due to this syndrome who has underwent a surgery in our hospital. CLINICAL DISCUSSION: Hematocolpos, the main symptom, is due to a retention of retained menstruation blood in women with obstructed hemivagina. Therefore, it's painful and associated with increasing dysmenorrhea (Brousse et al., n.d. [1]). The main treatment consists in its drainage with resection of vagina septum, preventing the patient from complications like endometriosis, infection, and infertility. CONCLUSION: A good knowledge of this anomaly can lead to an adequate diagnosis and more importantly an adequate treatment based on surgery to prevent the bad outcomes. |
format | Online Article Text |
id | pubmed-9189987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91899872022-06-14 Hematocolpos in women with uterus didelphys, imperforate hemivagina and ipsilateral renal agenesis: A case report and review of the literature M'hamdi, Oumaima Boujida, Sarah Bensghir, Ibtissam Baidada, Aziz Lakhdar, Amina Kharbach, Aicha Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Hematocolpos can be part of a rare syndrome OHVIRA or Herlyn-Werner-Wunderlich syndrome that requires special management (Brousse et al., n.d. [1]). The diagnosis can be delayed, yet an early diagnosis is important in order to elaborate an adequate strategy management and prevent the patient from complications. CASE PRESENTATION: We report the case of a 14-year-old girl suffering from an hematocolpos due to this syndrome who has underwent a surgery in our hospital. CLINICAL DISCUSSION: Hematocolpos, the main symptom, is due to a retention of retained menstruation blood in women with obstructed hemivagina. Therefore, it's painful and associated with increasing dysmenorrhea (Brousse et al., n.d. [1]). The main treatment consists in its drainage with resection of vagina septum, preventing the patient from complications like endometriosis, infection, and infertility. CONCLUSION: A good knowledge of this anomaly can lead to an adequate diagnosis and more importantly an adequate treatment based on surgery to prevent the bad outcomes. Elsevier 2022-06-06 /pmc/articles/PMC9189987/ http://dx.doi.org/10.1016/j.ijscr.2022.107277 Text en © 2022 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report M'hamdi, Oumaima Boujida, Sarah Bensghir, Ibtissam Baidada, Aziz Lakhdar, Amina Kharbach, Aicha Hematocolpos in women with uterus didelphys, imperforate hemivagina and ipsilateral renal agenesis: A case report and review of the literature |
title | Hematocolpos in women with uterus didelphys, imperforate hemivagina and ipsilateral renal agenesis: A case report and review of the literature |
title_full | Hematocolpos in women with uterus didelphys, imperforate hemivagina and ipsilateral renal agenesis: A case report and review of the literature |
title_fullStr | Hematocolpos in women with uterus didelphys, imperforate hemivagina and ipsilateral renal agenesis: A case report and review of the literature |
title_full_unstemmed | Hematocolpos in women with uterus didelphys, imperforate hemivagina and ipsilateral renal agenesis: A case report and review of the literature |
title_short | Hematocolpos in women with uterus didelphys, imperforate hemivagina and ipsilateral renal agenesis: A case report and review of the literature |
title_sort | hematocolpos in women with uterus didelphys, imperforate hemivagina and ipsilateral renal agenesis: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189987/ http://dx.doi.org/10.1016/j.ijscr.2022.107277 |
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