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Journal of Nursing Research and Practice

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Unicornuate uterus with rudimentary non-communicating cavitary horn in association VACTERL syndrome: Case report

Annual Congress on Midwifery nursing and Gynaecology

December 04-05, 2019 | Dubai, UAE

Abdelwahab Aleshawi

Jordan University of Science and Technology, Jordan

ScientificTracks Abstracts: J Nurs Res Pract

Abstract :

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 gynecologic and obstetric complications such as hematometra, endometriosis and ectopic pregnancy and thus surgical resection is usually advised. We have encountered 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 pediatric surgery and gynecology departments with three 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 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 regular period and the pain subsided completely. This is the second case of VACTERL association and unicornuate uterus with noncommunicating 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. In addition, it is preferable to explore for any associated congenital anomalies when performing any surgery for syndromic children.

Biography :

Abdelwahab Aleshawi is a 24-year-old organized graduated medical intern with an-excellent educational record, research skills and passion for health and wellbeing. He was graduated from Jordan University of Science and Technology (JUST). Now, he is an intern in King Abdulla University Hospital that is affiliated to JUST. He participated in many conferences and workshops that focus on gynecology and oncology. He has many ongoing researches and projects in the gynecology and oncology field. He looks forward a residency program in obstetrics and gynecology and to be pioneer, researcher and consultant in this field. He has 19 publisher articles.

E-mail: abdelwahhabjamal@yahoo.com

 
Google Scholar citation report
Citations : 50

Journal of Nursing Research and Practice received 50 citations as per Google Scholar report

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