scholarly journals Uterus didelphys with obstructed hemivagina and ipsilateral renal anomaly (OHVIRA syndrome): A case report

2014 ◽  
Vol 2 (9) ◽  
pp. 410-412 ◽  
Author(s):  
Mohamed Amin El-Gohary
Keyword(s):  
Case Report ◽  
Renal Anomaly ◽  
Uterus Didelphys ◽  
Ohvira Syndrome ◽  
Obstructed Hemivagina

Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome with septic shock: A case report

2018 ◽  
Vol 44 (7) ◽  
pp. 1326-1329 ◽  
Author(s):  
Masaki Kamio ◽  
Chikako Nagata ◽  
Hirotsugu Sameshima ◽  
Shinichi Togami ◽  
Hiroaki Kobayashi
Keyword(s):  
Septic Shock ◽  
Case Report ◽  
Renal Anomaly ◽  
Ohvira Syndrome ◽  
Obstructed Hemivagina

scholarly journals Possibilities of Early Ultrasound Diagnostics of the Herlin — Werner — Wunderlich syndrome (Case Report)

2021 ◽  
pp. 161-170
Author(s):  
F. Sh. Mamedova ◽  
E. A. Filippova ◽  
Z. K. Batyrova ◽  
Z. H. Kumykova
Keyword(s):  
Severe Pain ◽  
Pain Syndrome ◽  
Rare Type ◽  
Renal Anomaly ◽  
Genitourinary System ◽  
Uterus Didelphys ◽  
Ultrasound Diagnostics ◽  
Ohvira Syndrome ◽  
Obstructed Hemivagina ◽  
Instrumental Methods

Herlin — Werner — Wunderlich syndrome or OHVIRA (Obstructed hemivagina and ipsilateral renal anomaly) is a rare type of uterine and vaginal doubling defect (0,1 – 10,0 % of all uterine abnormalities) which is characterized by a triad of symptoms: uterus didelphys, unilateral obstructed hemivagina, and ipsilateral renal dysgenesis. The manifestation of the disease usually present after menarche, is accompanied by severe pain syndrome, leads to redoubted complications and organ-carrying operations with decreasing the fertility. At an earlier age, it can manifest itself as an infection of the genitourinary system. The diagnosis is based on clinical and anamnestic data using instrumental methods, the most accessible and safe of which is ultrasound. This article presents three clinical cases of patients 5 – 6 years old with a description of the ultrasound picture of the OHVIRA syndrome.

scholarly journals Management of Hematometra in Single Horn of Didelphic Uterus with Obstructed Hemivagina and Ipsilateral Renal Agenesis Syndrome: A Case Report with Brief Review of Literature

2016 ◽  
Vol 8 (3) ◽  
pp. 231-235
Author(s):  
Ritu Agarwal
Keyword(s):  
Case Report ◽  
South Asian ◽  
Renal Agenesis ◽  
Rare Entity ◽  
Review Of Literature ◽  
Resonance Imaging ◽  
Uterus Didelphys ◽  
Future Fertility ◽  
Ohvira Syndrome ◽  
Obstructed Hemivagina

ABSTRACT The triad of uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis (OHVIRA) syndrome is a rare entity. These cases are difficult to diagnose due to heterogeneous presentation and rarity of the condition. Ultrasonography and magnetic resonance imaging are important for initial diagnosis; however, laparoscopy is required for the confirmation of the diagnosis. Early and accurate diagnosis of this condition followed by prompt surgical therapy is essential to prevent complications and to preserve future fertility. Here we report a case of uterus didelphys with hemivagina and ipsilateral renal agenesis with hematometra and hematosalpinx in a young girl. How to cite this article Mishra VV, Agarwal R, Bandwal P, Choudhary S, Gandhi K. Management of Hematometra in Single Horn of Didelphic Uterus with Obstructed Hemivagina and Ipsilateral Renal Agenesis Syndrome: A Case Report with Brief Review of Literature. J South Asian Feder Obst Gynae 2016;8(3):231-235.

Abdominopelvic Pain in Patient with Uterus Didelphys and Unilateral Obstructed Hemivagina and Ipsilateral Renal Agenesis (OHVIRA Syndrome)

2021 ◽  
Author(s):  
Zahra Tavoli ◽  
Ali Montazeri
Keyword(s):  
Renal Agenesis ◽  
Primary Diagnosis ◽  
Case Presentation ◽  
Uterus Didelphys ◽  
Future Fertility ◽  
History Of ◽  
Ohvira Syndrome ◽  
Obstructed Hemivagina ◽  
Magnetic Resonance Imaging Mri

Introduction: Uterus didelphys with obstructed hemivagina associated with ipsilateral renal agenesis (OHVIRA syndrome) is a rare female urogenital malformation and delay in its diagnosis could lead to several complications. Case presentation: A 21-year-old virgin woman was admitted to the emergency department (ED) with severe abdominal pain, without fever and vaginal discharge. She reported a history of cyclic abdominopelvic pain and dysmenorrhea for 5 years. The primary diagnosis (OHVIRA syndrome) was made using ultrasonography, spiral computed tomography (CT) and magnetic resonance imaging (MRI). In addition, laparoscopy was performed to confirm diagnosis and drain hematosalpinx. Then, hysteroscopy was carried out for septum resection and catheter insertion. At one-month follow-up the ultrasonography showed normal left hemicavity of uterus associated with significant decrease in dysmenorrhea. Conclusion: Being aware of OHVIRA syndrome and clinical suspicion of this rare anomaly are essential for making a timely diagnosis, preventing complications, relieving symptoms, and preserving future fertility.

scholarly journals Hysteroscopic Resection of the Vaginal Septum in Uterus Didelphys with Obstructed Hemivagina: A Case Report

2007 ◽  
Vol 22 (4) ◽  
pp. 766 ◽  
Author(s):  
Tae Eun Kim ◽  
Gyoung Hoon Lee ◽  
Young Min Choi ◽  
Byung Chul Jee ◽  
Seung-Yup Ku ◽  
...  
Keyword(s):  
Case Report ◽  
Vaginal Septum ◽  
Uterus Didelphys ◽  
Obstructed Hemivagina ◽  
Hysteroscopic Resection

An unusual presentation of obstructed hemivagina and ipsilateral renal anomaly syndrome: A case report

2011 ◽  
Vol 54 (12) ◽  
pp. 820
Author(s):  
Woo-Oh Kim ◽  
Kyung Eui Park ◽  
Seung-Yup Ku ◽  
Seok Hyun Kim ◽  
Young Min Choi ◽  
...  
Keyword(s):  
Case Report ◽  
Unusual Presentation ◽  
Renal Anomaly ◽  
Obstructed Hemivagina
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