Congenital pouch colon with imperforate anus; a report of 3 cases
Journal of Qazvin University of Medical Sciences and Health Services [The]. 2006; 10 (1): 133-136
in Fa
| IMEMR
| ID: emr-78103
Responsible library:
EMRO
ABSTRACT
Congenital pouch colon [CPC] is an unusal condition in imperforate anus [IA] usually of high variety this malfotmation is mostly reported from India, where it comprises about 7% of all anorectal malformations. In this anomaly the normal colon is very short or absent and is replaced by a pouch like dilatation that usually communicates through a fistula with genitourinary tract or persistent cloaca. We are reporting on three cases of newborns [2 females, and 1 male] with this anomaly diagnosed during September 2001 to September 2004 These three cases comprise less than 3% of all cases of IA during this time period. The two girls had anorectal agenesia, short segment of colon and a pouch with vaginal fistula and persistent cloaca [Type II]. Colon in the third case was replaced by a dilated pouch that communicated with a wide fistula to the bladder [Type I]. This is very important for pediatric surgeons to be aware of the features of this condition to allow for proper diagnosis and surgical management
Search on Google
Index:
IMEMR
Main subject:
Anus, Imperforate
/
Rectum
/
Cloaca
/
Colonic Diseases
Type of study:
Case_reports
Limits:
Female
/
Humans
/
Male
Language:
Fa
Journal:
J. Qazvin Univ. Med. Sci. Health Serv.
Year:
2006