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Unicornuate uterus with a rudimentary non-communicating cavitary horn in association with VACTERL association: case report.
- Source :
-
BMC women's health [BMC Womens Health] 2019 May 30; Vol. 19 (1), pp. 71. Date of Electronic Publication: 2019 May 30. - Publication Year :
- 2019
-
Abstract
- Background: The unicornuate uterus is caused by abnormal or failed development of one Müllerian duct. Unicornuate uteri with functioning non-communicating rudimentary horns are susceptible to many gynaecologic and obstetric complications such as hematometra, endometriosis and ectopic pregnancy and thus surgical resection is usually recommended..<br />Case Presentation: We report a rare case of a unicornuate right uterus with rudimentary non-communicating (functional) cavitary left horn (class U4a) in a 17-year-old girl who was diagnosed with VACTERL association. She was presented to our centre with 3 years history of secondary sever dysmenorrhea. Pelvic magnetic resonance imaging revealed a normal uterus on the right side, a 7 × 8 cm left endometrioma, a tortuous dilated fluid-filled structure in the left hemipelvis, mostly represented left-sided hematosalpinx, and a well-defined lesion with thick enhancing wall in the left hemipelvis measuring 6.7 × 5.7 × 5.6 cm with a similar enhancement to the uterus in the right. She underwent laparotomy that showed a right unicornuate uterus with a normal cervix and a rudimentary non-communicating distended left horn. In addition, there was a left endometrioma and left hematosalpinx. Resection of the left communicating horn, left salpingectomy and left ovarian cystectomy were performed. The right tube and both ovaries were preserved. At 9-months follow up, the patient had a regular period and the pain subsided completely.<br />Conclusion: We report yet the second case of VACTERL association and unicornuate uterus with non-communicating functional rudimentary horn, in hope of expanding the knowledge of a rare occurrence. This case also highlights the importance of considering the diagnosis of Müllerian duct anomalies in patients with a history of other anomalies, and/or history of early-age secondary dysmenorrhea.
- Subjects :
- Adolescent
Anal Canal surgery
Dysmenorrhea etiology
Endometriosis etiology
Esophagus surgery
Female
Humans
Kidney surgery
Spine surgery
Trachea surgery
Anal Canal abnormalities
Esophagus abnormalities
Heart Defects, Congenital surgery
Kidney abnormalities
Limb Deformities, Congenital surgery
Mullerian Ducts abnormalities
Spine abnormalities
Trachea abnormalities
Subjects
Details
- Language :
- English
- ISSN :
- 1472-6874
- Volume :
- 19
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- BMC women's health
- Publication Type :
- Academic Journal
- Accession number :
- 31146728
- Full Text :
- https://doi.org/10.1186/s12905-019-0768-4