scholarly journals Multimodal ultrasound imaging of persistent urogenital sinus with uterus didelphys and double vagina malformation

Medicine ◽  
2021 ◽  
Vol 100 (52) ◽  
pp. e28477
Author(s):  
Yue Wang ◽  
Shourong Hu ◽  
Huifang Wang
PEDIATRICS ◽  
1962 ◽  
Vol 29 (5) ◽  
pp. 828-830
Author(s):  
Joseph Avin

A typical case of congenital adrenocortical hyperplasia with a persistent urogenital sinus has been followed for 9 years from the initiation of steroid therapy at 12 years, through surgical correction of the genital anomalies, a ruptured tubal pregnancy, and finally to the delivery of a normal female infant. The literature is briefly reviewed.


2007 ◽  
Vol 92 ◽  
pp. e48-e49 ◽  
Author(s):  
A. SAVANELLI ◽  
C. ESPOSITO ◽  
S. TILEMIS ◽  
A. FRANZESE ◽  
J. GUYS ◽  
...  

2010 ◽  
Vol 28 (4) ◽  
pp. 229-232 ◽  
Author(s):  
Joana Pauleta ◽  
Maria Antonieta Melo ◽  
Gertrudes Borges ◽  
Rui Carvalho ◽  
João Paulo Marques ◽  
...  

2010 ◽  
Vol 59 (2) ◽  
pp. 242-244 ◽  
Author(s):  
Sonia Singh ◽  
Poonam Singh ◽  
R.J. Singh

2016 ◽  
Vol 33 (05) ◽  
pp. e1-e1 ◽  
Author(s):  
Michela Giuliani ◽  
Benedetta Gui ◽  
Maria Laino ◽  
Viola Zecchi ◽  
Elena Rodolfino ◽  
...  

2019 ◽  
Vol 06 (10) ◽  
pp. 578-580
Author(s):  
Maaz Ahmed ◽  
Shalika Aeron Jayaswal ◽  
Sushma Malik

2014 ◽  
Vol 6 (4) ◽  
pp. 89-91
Author(s):  
Seema Chowdhary ◽  
Arvind Kumar Chowdhary ◽  
Sushma Pandey

Objective: Urogenital Sinus is a rare congenital deformity which overture to preclude of normal embryonic vaginal progression. We report a case of urogenital sinus with ambiguous genitalia in a female adult. Case Report:  An unmarried young female aged 26 years presented to our hospital with amenorrhea of 6 months and history of urinary incontinence from childhood. The diagnostic features of this case include normal haemogram with mildly elevated blood urea and creatinine, normal 17 ketosteroids, serum testosterone and DHEA; bilateral moderate hydronephrosis with uterus of size 6.8 x 4.6 x 5.3 cm; urogenital sinus with partial separation of bladder and vagina-vaginal type; bilateral hydrouretronephrosis with mild renal cortical scarring and bicornuate unicollis uterus cervix opening into the urogenital sinus. She was diagnosed with persistent urogenital sinus (Vaginal type) without congenital adrenal hyperplasia, but with associated mullerian anomaly. Treatment option was a U-shaped vaginoplasty with an aim of widening vaginal introitus and advancement of hypospadiac external urethral meatus to prevent micturition into vagina. Conclusion: Though the possible treatment options were discussed, this case study emphasizes the need of psycho social rehabilitation for the proper treatment of ambiguous genitalia. DOI: http://dx.doi.org/10.3126/ajms.v6i4.10107 Asian Journal of Medical Sciences Vol.6(4) 2015 89-91


2018 ◽  
Vol 17 (4) ◽  
pp. 455 ◽  
Author(s):  
Hooi H. Tan ◽  
Shung K. Tan ◽  
Rajah Shunmugan ◽  
Rozman Zakaria ◽  
Zakaria Zahari

Persistent urogenital sinus (PUGS) is a rare anomaly whereby the urinary and genital tracts fail to separate during embryonic development. We report a three-year-old female child who was referred to the Sabah Women & Children Hospital, Sabah, Malaysia, in 2016 with a pelvic mass. She had been born prematurely at 36 gestational weeks via spontaneous vaginal delivery in 2013 and initially misdiagnosed with neurogenic bladder dysfunction. The external genitalia appeared normal and an initial sonogram and repeat micturating cystourethrograms did not indicate any urogenital anomalies. She therefore underwent clean intermittent catheterisation. Three years later, the diagnosis was corrected following the investigation of a persistent cystic mass posterior to the bladder. At this time, a clinical examination of the perineum showed a single opening into the introitus. Magnetic resonance imaging of the pelvis revealed gross hydrocolpos and a genitogram confirmed a diagnosis of PUGS, for which the patient underwent surgical separation of the urinary and genital tracts.


2016 ◽  
Vol 04 (01) ◽  
pp. 013-016 ◽  
Author(s):  
Mario Lima ◽  
Francesca Destro ◽  
Noemi Cantone ◽  
Mohamed Shalaby ◽  
Giovanni Ruggeri

Persistent urogenital sinus (UGS) is a developmental anomaly. It represents one of the most complex problems that a pediatric surgeon may deal with. We report the case of a patient with UGS treated at 3 years of age by anterior sagittal transrectal approach and en bloc sinus mobilization. The procedure was performed with the patient prone with the initial idea of performing an anterior sagittal transrectal approach. The described approach allows an excellent anatomical view with a midline muscle sparing incision, along with an easy identification of the vaginal confluence with the benefit of avoiding dissection between the urethra and vagina.


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