POUCH COLON - Is a congenital condition in which all or part of colon is replaced by a pouch like dilated colonic structure that communicate distally with urogenital tract through a fistula .It is a rare high type anorectal malformation , with the size of pouch variable [ 5 to 15 cms ] . In this small bowel ( terminal ileum) opens into a blind pouch like colon . Rest of colon , rectum , anal canal & anus are missing . There is usually associated fistula connecting pouch to Genitourinary system.
TYPES OF POUCH COLON
Type 1- Absent normal colon & the terminal ileum opens into colonic pouch
Type 2 - The ileum opens into short segment of cecum which then opens into pouch
Type 3 - A significant length of normal colon is present between ileum & pouch
Type 4 - Near normal colon present with only part of colon [ rectum and sigmoid ] converted into a pouch
Below presented is rare type 1 pouch colon-
Clinicals- A day 2 neonate with distension abdomen & imperforate anus
Fig1- Abdominal radiograph of a day 2 neonate shows a large gas shadow occupying more than half of abdominal diameter, is a distended pouch colon, in a case of imperforate anus . The radiographic finding is classical & sufficient to diagnose this anomaly ( pouch colon) .
PS- The case study is intended for medical professionals for academic purposes.
- I express my sincere thanks to Dr Gaurav Bahety , M.Ch ( ped surgery) , Bhilwara for sharing this case & operative feedback .
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