Proctoneovaginohysterostomy and sigmoid colon pull-through for vaginal agenesis, hematocervicometra, and vestibular anus

1993 ◽  
Vol 6 (2) ◽  
pp. 95-98 ◽  
Author(s):  
Giovanni B. Candiani ◽  
Giuseppe Zaffaroni ◽  
Milena Dorta ◽  
Anna M. Fagnani ◽  
Massimo Candiani ◽  
...  
1992 ◽  
Vol 2 (04) ◽  
pp. 245-247 ◽  
Author(s):  
H. Takamatsu ◽  
H. Akiyama ◽  
H. Noguchi ◽  
H. Tahara ◽  
H. Kajiya
Keyword(s):  

Author(s):  
Pradyumna Pan

Background: The objective of this study is to report our experience with sigmoid vaginoplasty in adolescent female patients of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome with emphasis on the effectiveness of surgery, complications, sexual and functional outcomes.Methods: A retrospective study of adolescent females with vaginal atresia and Mayer-Rokitansky-Kuster-Hauser syndrome. The sigmoid segment was used for vaginoplasty in all the case.Results: Eleven females were studied over a period of 15 years. Postoperative complications were perineal rash in 3, ileus in 3, and minor wound infection in 1 patient and urinary tract infection in one patient. Nine patients were on regular follow-up. All the neovaginas were patent and functional. The postoperative mean vaginal length was 12.1 cm (range 11 cm to 14 cm). One of the patients had mild vaginal stenosis which responded to vaginal dilation, one had mucosal prolapse of the neovagina, one had excessive mucus discharge, during follow-up visits. Out of the 11patients, 8 patients are sexually active and 7 reported that they were engaging in satisfactory sexual activity with mild or no pain, and with good mucosal sensitivity. Only one experienced dyspareunia and three patients had not participated in sexual activity.Conclusions: Sigmoid vaginoplasty is a safe and acceptable procedure for vaginal agenesis with good cosmetic results and acceptable complications rate. Sigmoid colon vaginoplasty is the treatment of choice because of its large lumen, thick walls resistant to trauma, adequate secretion allowing lubrication, not demanding prolonged dilatation and short recovery time.


2020 ◽  
Vol 7 (3) ◽  
pp. 904
Author(s):  
Manisha Albal ◽  
Prasad Y. Bansod ◽  
Mahendra Chauhan

Mullerian duct anomalies are rare and can present with abnormalities in upper vagina, cervix, uterus, and fallopian tubes. The exact incidence of cervicovaginal agenesis is unknown and there are very few cases recorded in the literature. Authors report a 12-year-old girl referred from gynaecologist with chronic cyclical abdominal pain with underdeveloped, geniatilia and developed secondary sexual characters. Radiological investigations showed hypoplastic cervix with hematometra and left hemato salpinx. A definitive repair with creation of a neovagina using a sigmoid colon segment was performed in a single stage. Many techniques are described for reconstruction of cervicovaginal canal. Use of colon in creation of a neovagina is described by authors. Here we report a case of complete vaginal agenesis presenting with Hematometra-Hematosalpinx where a neovagina was created using a segment of sigmoid colon. Single staged surgery for neovagina creation using segment of sigmoid colon offers a promising and safe alternative for cervicovaginal agenesis. 


2018 ◽  
Vol 13 (2) ◽  
Author(s):  
Lubna Razzak ◽  
Raheela Mohsin Rizvi

Case: A female aged 22 years, suffering from cyclical menouria since age of 12 years presented to our clinic with concerns for future sexuality and fertility. Clinical examination revealed the absence of a vagina, although labia minora and majora were adequately developed. Secondary sexual growth such as axillary and pubic hair, breast development was normal. Micturating cystogram shows abnormal fistulous communication between the posterior urethra and upper vagina with contrast outlining the uterine cavity. Magnetic resonance imaging revealed functioning left kidney along with vaginal agenesis and an abnormal communication between uterus and urethra. The surgical treatment included urethrovaginal fistula repair   and pull through vaginoplasty.  The patient was asymptomatic till her last visit Conclusions: In this case, the diagnosis of congenital urethrovaginal fistula was delayed until adulthood despite menouria. This is a rare case report and to our best of literature search .we could not find any such case report.


2010 ◽  
Vol 15 (1) ◽  
pp. 19 ◽  
Author(s):  
Jiledar Rawat ◽  
Intezar Ahmed ◽  
Anand Pandey ◽  
TanvirR Khan ◽  
Sarita Singh ◽  
...  

1977 ◽  
Vol 3 (2) ◽  
pp. 57-61 ◽  
Author(s):  
G. Rutishauser ◽  
M. Dürig ◽  
B. Leibundgut ◽  
P. Evard ◽  
P. Graber

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