Anal sphincter reconstruction with a pudendal nerve anastomosis following abdominoperineal resection

1997 ◽  
Vol 40 (12) ◽  
pp. 1497-1503 ◽  
Author(s):  
Tomoyuki Sato ◽  
Fumio Konishi ◽  
Kyotaro Kanazawa
2005 ◽  
Vol 48 (11) ◽  
pp. 2085-2089 ◽  
Author(s):  
Nicolas Pirro ◽  
Igor Sielezneff ◽  
Andrew Malouf ◽  
Medhi Ouaïssi ◽  
Vincent Di Marino ◽  
...  

1999 ◽  
Vol 42 (4) ◽  
pp. 451-456 ◽  
Author(s):  
Philippe Rouanet ◽  
Pierre Senesse ◽  
Dalila Bouamrirene ◽  
Eliane Toureille ◽  
Michel Veyrac ◽  
...  

Surgery ◽  
2000 ◽  
Vol 127 (1) ◽  
pp. 92-98 ◽  
Author(s):  
Tomoyuki Sato ◽  
Fumio Konishi ◽  
Kyotaro Kanazawa

1974 ◽  
Vol 2 (2) ◽  
pp. 133-141 ◽  
Author(s):  
G. Freilinger ◽  
H. Holle ◽  
B. Mamoli

2020 ◽  
Vol 47 (3) ◽  
pp. 272-276
Author(s):  
Chairat Burusapat ◽  
Natthawoot Hongkarnjanakul ◽  
Nutthapong Wanichjaroen ◽  
Sakchai Panitwong ◽  
Jiraporn Sangkaewsuntisuk ◽  
...  

Anorectal malformation or imperforate anus is a congenital anomaly of rectum and anus. Mullerian duct anomalies are abnormal development of uterus, cervix, and vagina. Imperforate anus with double uterus is extremely rare and cannot explain by normal embryologic development. Moreover, guideline in treatment is inconclusive. We report an extremely rare case of a young adult female who presented with recurrent pelvic inflammatory disease caused by rectovaginal fistula in congenital imperforate anus and didelphys uterus, and successfully neoanal reconstruction with gracilis muscle flap. Aims for treatment are closed rectovaginal fistula, and anal sphincter reconstruction. To our best knowledge, the imperforate anus with double uterus is extremely rare anomaly. Furthermore, successfully anal sphincter reconstruction with functional gracilis muscle in the imperforate anus with double uterus has never been reported in English literature.


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