scholarly journals A Rare Case of Herlyn-Werner-Wünderlich Syndrome with an Ectopic Ureter and A Communication Between a Hydrocolpos and The Bladder Neck in A Uterus Didelphys

2021 ◽  
Vol 04 (05) ◽  
Author(s):  
Maañón di Leo JC ◽  
Cruz FJMS ◽  
Mármol RL ◽  
Knowlson NG ◽  
García JMM
Keyword(s):  
Bladder Neck ◽  
Rare Case ◽  
Ectopic Ureter ◽  
Uterus Didelphys

scholarly journals A rare case presentation of an anomalous uterus mimicking ovarian tumour

2017 ◽  
Vol 6 (6) ◽  
pp. 2638
Author(s):  
Mohanambal M. ◽  
Wills G. Sheelaa
Keyword(s):  
Rare Case ◽  
Pregnancy Loss ◽  
Recurrent Pregnancy Loss ◽  
Ovarian Tumour ◽  
Left Ovary ◽  
Unusual Presentation ◽  
Case Presentation ◽  
Young Girls ◽  
Uterus Didelphys ◽  
Operative Findings

Mullerian anomalies occur in 1:1000-3000 females. Uterus didelphys and obstructed hemangioma with a septum contribute to 10% anomalies. Young girls present with severe dysmenorrhea, hematometra, hematocolpos and recurrent pregnancy loss. A 16-year-old teenager presented like a torsion of complex ovarian tumour is presented here. Intra operative findings was uterus didelphys with well-developed 2 horns, tubes and ovaries. On left ovary, a hemorrhagic corpus luteal cyst of size 5.2*4cm was seen with 50ml of hemoperitoneum. Diagnosis was confirmed histopathologically. This case is reported for the unusual presentation of an anomalous uterus mimicking torsion ovarian tumour.

A Case of Unique Communication Between Blind-Ending Ectopic Ureter and Ipsilateral Hemi-Hematocolpometra in Uterus Didelphys

1995 ◽  
Vol 153 (4) ◽  
pp. 1208-1210 ◽  
Author(s):  
Takashi Shibata ◽  
Katsuya Nonomura ◽  
Hidehiro Kakizaki ◽  
Masahide Murayama ◽  
Toshimori Seki ◽  
...  
Keyword(s):  
Ectopic Ureter ◽  
Uterus Didelphys ◽  
Blind Ending

Bilateral Single System Ectopic Ureter with Urolithiasis: A Rare Case Entity

2016 ◽  
Vol 83 (4) ◽  
pp. 218-220
Author(s):  
Ankur Bansal ◽  
Manoj Kumar ◽  
Ashok Sokhal ◽  
Bimalesh Purkait ◽  
Gautam Kanodia
Keyword(s):  
Rare Case ◽  
Ectopic Ureter ◽  
Single System

scholarly journals EPISPADIAS IN GIRLS

2019 ◽  
Vol 23 (3) ◽  
pp. 166-168
Author(s):  
A. E. Soloviev
Keyword(s):  
Quality Of Life ◽  
Urinary Incontinence ◽  
Surgical Treatment ◽  
Plastic Surgery ◽  
Clinical Picture ◽  
Bladder Neck ◽  
Rare Case ◽  
Diagnosis And Treatment ◽  
X Ray

Purpose. To study the clinical picture, diagnosis and treatment of epispadias in girls. Material and methods. 22 girls with epispadias of various forms were under supervision for 50 years. During diagnostics the following issues were used: anamnesis, examination, catheterization and uroflowmetry, cystoscopy of the bladder, ultrasound and X-ray examination. Results and discussion. Out of 22 girls with epispadias, clitoral epispadia (partial ) was in 10 patients; sub-symphisal (subtotal) - in 4; symphisal (total) - in 8 girls. In 10 girls with the clitoral form, urological examination was made because of changes in the urine. Girls with sub-symphisal epispadia complained of irritation and itching in the vulva. All had vulvitis, cystitis, chronic pyelonephritis. In 2 patients, renal doubling was diagnosed; in other 2 patients ureterohydronephrosis and kidney dystopia were diagnosed. Uroflowmetry revealed hyperactive bladder in all. 8 girls with the total (symphisial) form of epispadia and urinary incontinence were operated by the Derzhavin technique; after the surgery the function of bladder sphincter was restored and the patients could have a normal quality of life. Conclusion. Epispadia in girls is a rare case . There are clitoral, sub-symphisal and symphisal (total) forms of epispadias. Cluster and sub-symphisial forms do not require surgical treatment. While in the symphisial (total) form, plastic surgery on the bladder neck by the Derzhavin technique is recommended. It is a good option for recovery.

scholarly journals Rupture Uterus in Pregnancy with Didelphys Uterus: A Rare Case Report

2011 ◽  
Vol 3 (3) ◽  
pp. 149-150 ◽  
Author(s):  
Shaifali Dadhich ◽  
Shashi Suthar ◽  
Rekha Choudhary
Keyword(s):  
Case Report ◽  
Perinatal Outcome ◽  
Rare Case ◽  
Previous Cesarean Section ◽  
Uterus Didelphys ◽  
Rare Case Report ◽  
History Of ◽  
Ruptured Uterus ◽  
In Pregnancy ◽  
Previous Cesarean

ABSTRACT Uterus didelphys is rare and sometimes not even diagnosed. We report a case of didelphys uterus in a 26-year-old pregnant lady who previously had three successful pregnancies with previous one C-section and remained undiagnosed till she presented to us as ruptured uterus. This case report aimed to summarize the clinical characteristics and perinatal outcome of VBAC in pregnancy with didelphys uterus and history of previous cesarean section.

scholarly journals Uterus didelphys associated with ovarian endometriosis in an infertile patient

2019 ◽  
Vol 76 (7) ◽  
pp. 749-752
Author(s):  
Ivana Rudic-Biljic-Erski ◽  
Mladenko Vasiljevic ◽  
Snezana Rakic ◽  
Olivera Dzatic-Smiljkovic ◽  
Sladjana Mihajlovic
Keyword(s):  
Rare Case ◽  
Transvaginal Ultrasound ◽  
Resonance Imaging ◽  
Laparoscopic Treatment ◽  
Hormone Analogue ◽  
Ovarian Endometriosis ◽  
Incision And Drainage ◽  
Uterus Didelphys ◽  
Pelvic Exam ◽  
Endometriotic Cyst

Introduction. Uterus didelphys results when Mullerian duct fusion is completely arrested during development. We presented a rare case of nonobstructive uterus didelphys occurring simultaneously with an endometriotic cyst of the ovary. Case report. A twenty-nine-year-old, nulliparous patient was admitted to our Clinic for laparoscopic treatment of an endometriotic ovarian cyst. Diagnoses of right ovarian endometriotic cyst and nonobstructed uterus didelphys were established with bimanual pelvic exam and two-dimensional transvaginal ultrasound. Diagnoses were subsequently confirmed by laparoscopy and magnetic resonance imaging. Laparoscopic incision and drainage of the endometriotic cyst were performed, followed by biopsy and coagulation of endometriotic lesions. Histopathology confirmed ovarian endometriosis. Gonadotropinreleasing hormone analogue (GnRHa) was prescribed postoperatively, for a total of 3 months. Ten months after completion of treatment, the patients was without disease recurence. Conclusion. Nonobstructive uterus didelphys is rarely associated with ovarian endometriosis.

scholarly journals A rare case of uterus didelphys presented as secondary abdominal pregnancy

2013 ◽  
Vol 2 (4) ◽  
pp. 737
Author(s):  
Neena Gupta ◽  
Sachidanand Gupta ◽  
Neetu Singh ◽  
Arun Arya ◽  
Pavika Lal ◽  
...  
Keyword(s):  
Rare Case ◽  
Abdominal Pregnancy ◽  
Uterus Didelphys

scholarly journals Rare case presentation of leiomyoma of bladder neck with tuberculous pelvic lymphadenitis in a young female patient

2021 ◽  
Vol 34 ◽  
pp. 101436
Author(s):  
Mahmoud Moawad ◽  
Najla Ben Ghashir ◽  
Quatullah Rustum ◽  
Hamid Toussi
Keyword(s):  
Female Patient ◽  
Bladder Neck ◽  
Rare Case ◽  
Young Female ◽  
Case Presentation
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