scholarly journals A rare case of hydrometrocolpos from persistent urogenital sinus in patient affected by adrenogenital syndrome

2018 ◽  
Vol 21 (3) ◽  
pp. 249-252
Author(s):  
Igino Simonetti ◽  
Piero Trovato ◽  
Francesco Verde ◽  
Luca Tarotto ◽  
Roberto Della Casa ◽  
...  
2021 ◽  
Vol 3 (3) ◽  
pp. 280-283
Author(s):  
Mohamed Ibrahim Amer ◽  

Persistent urogenital sinus (PUGS) is an uncommon developmental cloacal anomaly, with Incidence of 0.6 in 10000 female births. Herein we depict the case of a 22-year of age lady who presented with Infertility for 16 months with dyspareunia and was found to have Persistent urogenital sinus associated with other urogenital anomalies as unilateral rudimentary horn with ipsilateral renal agenesis and contralateral dermoid cyst. The patient was successfully treated with the excision of the sinus, the rudimentary horn and the dermoid cyst.


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


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