scholarly journals Congenital pouch colon in girls: An algorithm for preoperative diagnosis

2022 ◽  
Vol 27 (1) ◽  
pp. 71
Author(s):  
Amit Gupta ◽  
Amit Kumar ◽  
Rajiv Chadha ◽  
PartapSingh Yadav ◽  
Vikram Khanna ◽  
...  
Keyword(s):  
Preoperative Diagnosis ◽  
Congenital Pouch Colon ◽  
Pouch Colon

scholarly journals Newer variant of congenital pouch colon with double colovesical fistulae

2012 ◽  
Vol 17 (2) ◽  
pp. 89
Author(s):  
Archana Puri ◽  
Monica Nanda ◽  
R Chadha ◽  
SRoy Choudhary
Keyword(s):  
Congenital Pouch Colon ◽  
Pouch Colon

scholarly journals Congenital pouch colon

2011 ◽  
Vol 31 (5) ◽  
pp. 546-547 ◽  
Author(s):  
Bilal Mirza ◽  
Lubna Ijaz ◽  
Afzal Sheikh
Keyword(s):  
Congenital Pouch Colon ◽  
Pouch Colon

scholarly journals Varied Presentation of Congenital Segmental Dilatation of the Intestine in Neonates: Report of Three Cases

2016 ◽  
Vol 5 (4) ◽  
pp. 55 ◽  
Author(s):  
Binod Kumar Rai ◽  
Bilal Mirza ◽  
Imran Hashim ◽  
Muhammad Saleem
Keyword(s):  
Intestinal Obstruction ◽  
Anorectal Malformation ◽  
Developmental Anomaly ◽  
Abdominal Radiograph ◽  
Abdominal Drain ◽  
The Third ◽  
Neonatal Intestinal Obstruction ◽  
Segmental Dilatation ◽  
Congenital Pouch Colon ◽  
Pouch Colon

Congenital segmental dilatation (CSD) of the intestine is a rare developmental anomaly characterized by sharply demarcated dilatation of a gastrointestinal segment and may present with intestinal obstruction. We report three cases of CSD of the intestine in neonates with varied presentation. First patient was mistaken as pneumoperitoneum on abdominal radiograph, which led to initial abdominal drain placement. The 2nd patient was a case of anorectal malformation associated with congenital pouch colon (CPC) and CSD of ileum; and the third case presented as neonatal intestinal obstruction and found to have CSD of ileum. All the patients were successfully managed in our department.

scholarly journals Use of congenital pouch colon for augmenting the neurogenic bladder in a child: a 13-year follow-up

2015 ◽  
Vol 2015 (mar12 1) ◽  
pp. bcr2014208486-bcr2014208486 ◽  
Author(s):  
J. J. Kurian ◽  
H. S. Bal ◽  
S. Sen
Keyword(s):  
Neurogenic Bladder ◽  
Congenital Pouch Colon ◽  
Pouch Colon

A Female Patient with Congenital Pouch Colon (CPC): a Case Report

2011 ◽  
Vol 111 (5) ◽  
pp. 335-337 ◽  
Author(s):  
O. Yilmaz ◽  
A. Genc ◽  
S. Ayhan ◽  
T. Ozcan ◽  
R. Aygoren ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Congenital Pouch Colon ◽  
Pouch Colon

scholarly journals Type V Pouch Colon, Prune Belly Syndrome, and Congenital Anterior Urethrocutaneous Fistula

2017 ◽  
Vol 6 (2) ◽  
pp. 38 ◽  
Author(s):  
Prince Raj ◽  
Hirendra Birua
Keyword(s):  
Anorectal Malformation ◽  
Male Child ◽  
Prune Belly Syndrome ◽  
Urethrocutaneous Fistula ◽  
Rare Type ◽  
Prune Belly ◽  
Short Colon ◽  
Congenital Pouch Colon ◽  
Pouch Colon ◽  
Type V

Congenital pouch colon (CPC) or short colon syndrome is a rare type of anorectal malformation(ARM). Type V is the rarest form of CPC. We present a 1-day-old male child with type V CPC with prune belly syndrome and congenital anterior urethrocutaneous fistula (CAUF).

Sign in / Sign up

Export Citation Format

Share Document