scholarly journals Bicornuate Uterus with Complete Cervico-Vaginal Agenesis and Skeletal Deformity: A Case Report

2018 ◽  
Vol 69 (S1) ◽  
pp. 67-70
Author(s):  
Jyoti Meena ◽  
Juhi Bharti ◽  
Kallol Kumar Roy ◽  
Sunesh Kumar ◽  
Seema Singhal ◽  
...  
Keyword(s):  
Case Report ◽  
Vaginal Agenesis ◽  
Skeletal Deformity ◽  
Bicornuate Uterus

scholarly journals Massive Hematometra due to Congenital Cervicovaginal Agenesis in an Adolescent Girl Treated by Hysterectomy: A Case Report

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Turki Gasim ◽  
Fathia E. Al Jama
Keyword(s):  
Case Report ◽  
Adolescent Girl ◽  
Abdominal Hysterectomy ◽  
Left Ovary ◽  
Mentally Handicapped ◽  
Vaginal Agenesis ◽  
Bicornuate Uterus

A case of massive hematometra with a bicornuate uterus in a 14-year-old mentally handicapped girl complicated by vaginal agenesis and absent cervix is presented. She was managed by abdominal hysterectomy and right salpingo-oophorectomy that included the ovarian cystadenoma. The left ovary was conserved. This treatment was considered appropriate for this patient.

scholarly journals Pregnancy: CASE REPORT Twin gestation occupying separate horns of a bicornuate uterus after in-vitro fertilization and embryo transfer

1996 ◽  
Vol 11 (10) ◽  
pp. 2316-2318 ◽  
Author(s):  
L.I. Barmat ◽  
M.A. Damario ◽  
A. Kowalik ◽  
I. Kligman ◽  
O.K. Davis ◽  
...  
Keyword(s):  
Case Report ◽  
In Vitro Fertilization ◽  
Embryo Transfer ◽  
Bicornuate Uterus ◽  
Vitro Fertilization

scholarly journals Acute Kidney Injury After Sigmoid Vaginoplasty Procedure In Mullerian Duct Anomalies: A Case Report

2021 ◽  
Vol 04 (04) ◽  
Author(s):  
Rizkha Adistyatama ◽  
Keyword(s):  
Acute Kidney Injury ◽  
Abdominal Pain ◽  
Case Report ◽  
European Society ◽  
Surgical Procedure ◽  
Kidney Injury ◽  
Vaginal Agenesis ◽  
Müllerian Duct Anomalies ◽  
Sigmoid Vaginoplasty ◽  
Mullerian Duct Anomalies

Background: Development of female genital tract is a complex process and dependent upon a series of events involving cellular differentiation, migration, fusion, and canalization. Mullerian Duct Anomalies (MDA) are uncommon congenital anomalies, but can vary widely and treatable with surgical procedure. Classification system that have been used are classification from American Society for Reproductive Medicine (ASRM) and European Society of Human Reproduction and Embriology (ESHRE) and European Society for Gynaecological Endoscopy (ESGE). Surgical procedure in MDA patient had a high successful rate, but postoperative complication can arise in form of the need for further surgical requirement and acute kidney injury. Case report: A 20 year old girl admitted to obstetric gynecologic clinic with complaints of abdominal pain, amenorrhea, and redness voiding. She experienced abdominal pain since 6 years ago. Previously, patient had history of vaginal drainage procedure when she was 14 years old but she did not felt improvement in complaint and symptom. Cystoscopy and radiology imaging showed vaginal agenesis and renal dekstra agenesis, subsequently patient was planned for a sigmoid vaginoplasty procedure. Identification and exploration during surgery revealed vaginal agenesis, renal dekstra agenesis, hematometra from hemiuterus dekstra, hemiuterus sinistra with asesorius or hipoplasia uterine and hematosalping dekstra. In 5 days post operative, patient suffer anuria and acute kidney injury complication. Acute kidney injury after major surgery involving gastrointestinal was common because of surgical stress response, and agenesis renal condition aggravates this complication.

scholarly journals (Ventrodorsal) Symmetrical Bicornuate Uterus Mimicking a Pedunculated Myoma—A Case Report

2017 ◽  
Vol 05 (04) ◽  
pp. 33-38
Author(s):  
Adam Moyosore Afodun ◽  
Khadijah Kofoworola Quadri ◽  
Mustapha Akajewole Masud ◽  
Muhammad Olanrewaju Buhari ◽  
Sodiq Kolawole Lawal
Keyword(s):  
Case Report ◽  
Bicornuate Uterus

scholarly journals Twin pregnancy in a bicornuate uterus in rural Kenya: A case report for accidental discovery and successful delivery

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Hussein E. Elias ◽  
James A. Amisi
Keyword(s):  
Case Report ◽  
Twin Pregnancy ◽  
Mode Of Delivery ◽  
Vital Signs ◽  
Rare Occurrence ◽  
Middle Income ◽  
Bicornuate Uterus ◽  
Increased Risk ◽  
Uterine Anomalies ◽  
Adverse Pregnancy

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.

Sign in / Sign up

Export Citation Format

Share Document