Twin Pregnancy in Bicornuate Uterus–One Fetus in Each Horn

2018 ◽  
Vol 5 (1) ◽  
pp. 59-61
Author(s):  
Mohd Ilyas ◽  
Mohammad Saleem Dar ◽  
Suhail Rafiq ◽  
Insha Khan
Author(s):  
Hussein E. Elias ◽  
James A. Amisi

Introduction: Uterine anomalies are often identified during pregnancy, during infertility evaluation or pregnancy miscarriage and have been associated with an increased risk of adverse pregnancy outcomes. Although some studies have documented the rare occurrence of spontaneous twin pregnancy in each horn of a bicornuate uterus, this is the first time this is being documented in Kenya, to the best of our knowledge. This is a rare occurrence and reporting of this case adds to the documentation of such cases.Patient presentation: This is a case report for a 30-year-old female, para 2+0 at 34 weeks 4 days by dates, who presented with features of labour. Upon examination, she had normal vital signs and a fundal height of 38 weeks with multiple foetal parts both in cephalic presentation and two foetal heart rates within normal range. Her antenatal profile was non-contributory and had undergone two ultrasounds that confirmed twin gestation with no other notable findings.Management and outcome: The patient had a spontaneous vertex delivery of the first twin with a good outcome. There was a delay in the delivery of the second twin and a caesarean section was done with an indication of non-reassuring foetal status and low-lying placenta. The bicornuate uterus was accidentally identified during the surgery. The outcome was good, with an APGAR score of 6 in the first minute and 9 at 10 min.Conclusion: Although this is a rare occurrence, we would like to sensitise healthcare workers in rural low- to middle-income countries that this can occur, and they should attempt to increase antenatal diagnosis as it can influence the mode of delivery.


2006 ◽  
Vol 86 (6) ◽  
pp. 1764.e3-1764.e5 ◽  
Author(s):  
Angel Chao ◽  
An-Shine Chao ◽  
Shih-Tíen Wang ◽  
Tzu-Hao Wang

Author(s):  
Juan Mario Troyano-Luque ◽  
Margarita Álvarez de la Rosa ◽  
Ana Isabel Padilla ◽  
Laura Ces ◽  
José María Martínez ◽  
...  

Abstract A female fetus of a dizygotic pregnancy presented with a retrovesical cystic mass at 16 weeks. Severe and recurrent fetal ascitis developed at 25 weeks. Pre-eclampsia, probably due to mirror syndrome, precipitated fetal extraction, which led to severe prematurity complications and neonatal death. Necropsy showed: cloacal anomaly, anal atresia, ambiguous genitalia and bicornuate uterus.


2011 ◽  
Vol 33 (2) ◽  
pp. 142-144 ◽  
Author(s):  
Mireia Cruceyra ◽  
Carlos Iglesias ◽  
María De La Calle ◽  
Marta Sancha ◽  
Sara López Magallón ◽  
...  

Author(s):  
Verma Ruchi ◽  
◽  
Patel Shweta ◽  
Mishra Neha ◽  
Gupta Veena ◽  
...  

The rupture of uterus in first and second trimester is very rare and mostly associated with uterine anomalies or cornual pregnancy. Bicornuate uterus (BU) is a uterine anomaly results from incomplete fusion of the two Mullerian ducts during embryogenesis. Here we are presenting a case of primigravida in the second trimester (20 weeks) as ruptured ectopic pregnancy in emergency. Laparotomy showed BU with twin pregnancy in the ruptured non communicating right horn. Right horn excision was done. This case highlights the twin pregnancy in non-communicating horn of uterus and its rupture in early pregnancy. Cases with non-communicating horn are reported but twin pregnancy in noncommunicating horn is a rare one. In asymptomatic women, the presence of bicornuate uterus may not be detected until during pregnancy or delivery. In case of pregnancy in rudimentary horn, early sonographic diagnosis has a major contribution in evaluation and management. Treatment usually involved is resection of the ruptured horn. Since the scar is present on the uterus, it is important to avoid pregnancy for at least 1 year.


1979 ◽  
Vol 7 (4) ◽  
pp. 303-304 ◽  
Author(s):  
William M. Green ◽  
Suzanne Berry ◽  
Gerardine Wilkinson

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