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Cervical Dysgenesis: A Rare Mullerian Duct Anomaly
Cervical agenesis or dysgenesis is a rare congenital anomaly. The patients usually present with primary amenorrhoea, primary infertility, and cyclical abdominal pain or with a history of prior surgeries like hymenectomy, vaginoplasty, or adhesiolysis for endometriosis along with well developed secon...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8544906/ https://www.ncbi.nlm.nih.gov/pubmed/34722057 http://dx.doi.org/10.7759/cureus.18279 |
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author | Samantaray, Subha R Mohapatra, Ipsita |
author_facet | Samantaray, Subha R Mohapatra, Ipsita |
author_sort | Samantaray, Subha R |
collection | PubMed |
description | Cervical agenesis or dysgenesis is a rare congenital anomaly. The patients usually present with primary amenorrhoea, primary infertility, and cyclical abdominal pain or with a history of prior surgeries like hymenectomy, vaginoplasty, or adhesiolysis for endometriosis along with well developed secondary sexual characters. We present a case of 15 years old girl with cervical dysgenesis and proximal vaginal agenesis, who presented with severe cyclical abdominal pain. She was managed with cervicovaginal canalization by coring and drilling technique done by vaginal approach with simultaneous laparoscopic guidance. Being a rare type of developmental anomaly of the female genital tract, no standard treatment for type-2 cervical dysgenesis has been established. The patient was followed up for 18 months during which she reported to be having regular menstruation. |
format | Online Article Text |
id | pubmed-8544906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-85449062021-10-28 Cervical Dysgenesis: A Rare Mullerian Duct Anomaly Samantaray, Subha R Mohapatra, Ipsita Cureus Obstetrics/Gynecology Cervical agenesis or dysgenesis is a rare congenital anomaly. The patients usually present with primary amenorrhoea, primary infertility, and cyclical abdominal pain or with a history of prior surgeries like hymenectomy, vaginoplasty, or adhesiolysis for endometriosis along with well developed secondary sexual characters. We present a case of 15 years old girl with cervical dysgenesis and proximal vaginal agenesis, who presented with severe cyclical abdominal pain. She was managed with cervicovaginal canalization by coring and drilling technique done by vaginal approach with simultaneous laparoscopic guidance. Being a rare type of developmental anomaly of the female genital tract, no standard treatment for type-2 cervical dysgenesis has been established. The patient was followed up for 18 months during which she reported to be having regular menstruation. Cureus 2021-09-25 /pmc/articles/PMC8544906/ /pubmed/34722057 http://dx.doi.org/10.7759/cureus.18279 Text en Copyright © 2021, Samantaray et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Obstetrics/Gynecology Samantaray, Subha R Mohapatra, Ipsita Cervical Dysgenesis: A Rare Mullerian Duct Anomaly |
title | Cervical Dysgenesis: A Rare Mullerian Duct Anomaly |
title_full | Cervical Dysgenesis: A Rare Mullerian Duct Anomaly |
title_fullStr | Cervical Dysgenesis: A Rare Mullerian Duct Anomaly |
title_full_unstemmed | Cervical Dysgenesis: A Rare Mullerian Duct Anomaly |
title_short | Cervical Dysgenesis: A Rare Mullerian Duct Anomaly |
title_sort | cervical dysgenesis: a rare mullerian duct anomaly |
topic | Obstetrics/Gynecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8544906/ https://www.ncbi.nlm.nih.gov/pubmed/34722057 http://dx.doi.org/10.7759/cureus.18279 |
work_keys_str_mv | AT samantaraysubhar cervicaldysgenesisararemullerianductanomaly AT mohapatraipsita cervicaldysgenesisararemullerianductanomaly |