Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome – A Case ReportRT

Authors

  • Md. Kabirul Islam Square Hospitals Ltd Dhaka
  • Md. Shah Alam Dhaka Medical College Hospital Dhaka
  • Abdul Hanif Dhaka Medical College Hospital Dhaka
  • Md. Kamrul Hasan Dhaka Medical College Hospital Dhaka
  • Mizanur Rahman Bangabandhu Sheikh Mujib Medical University Dhaka

DOI:

https://doi.org/10.3329/jpsb.v1i1.19468

Keywords:

MRKH, vaginal malformation

Abstract

We report a case of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome in a 25 year old married lady. Though it is a congenital abnormality, she presented as primary infertility after 2 year of her marriage and was referred to us from a Gynaecologist. She had absent vagina, rudimentary uterus with no cervix. Her ovaries were severely hypoplastic. The anus was placed anteriorly and opened into the vulva. In spite of absence of her vagina, the lady somehow maintained her married life by doing intercourse through the anteriorly placed rectum. The vagina was made from the lower end of existing rectum which opened into the vulva. The proximal end of the rectum and left colon were pulled through the pelvis and opened into the perineum. It improved her quality of life.

DOI: http://dx.doi.org/10.3329/jpsb.v1i1.19468

 

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Author Biographies

Md. Kabirul Islam, Square Hospitals Ltd Dhaka

Department of Pediatric Surgery

Md. Shah Alam, Dhaka Medical College Hospital Dhaka

Department of Pediatric Surgery

Abdul Hanif, Dhaka Medical College Hospital Dhaka

Department of Pediatric Surgery

Md. Kamrul Hasan, Dhaka Medical College Hospital Dhaka

Department of Pediatric Surgery

Mizanur Rahman, Bangabandhu Sheikh Mujib Medical University Dhaka

Department of Pediatric Surgery

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Published

2014-07-09

How to Cite

Islam, M. K., Alam, M. S., Hanif, A., Hasan, M. K., & Rahman, M. (2014). Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome – A Case ReportRT. Journal of Paediatric Surgeons of Bangladesh, 1(1), 70–73. https://doi.org/10.3329/jpsb.v1i1.19468

Issue

Section

Case Reports