Antenatal diagnosis of congenital pouch colon: a case report from the Indian subcontinent with insights into management
Jitendra Sharma, Rajesh Malik, Reyaz Ahmed

TL;DR
This case report describes the rare antenatal diagnosis of congenital pouch colon in a fetus, leading to timely treatment and a successful recovery.
Contribution
The paper presents a rare case of antenatal CPC diagnosis and highlights its impact on improved clinical outcomes.
Findings
CPC was suspected via ultrasound in the late third trimester due to a hypoechoic tubular lesion in the pre-sacral region.
Early diagnosis allowed for timely delivery and surgery, reducing complications and improving recovery.
The child underwent staged corrective surgeries and made a complete recovery.
Abstract
Congenital pouch colon (CPC) is highly uncommon congenital anorectal malformation where a distended pouch-like structure replaces either some part of the colon or the entire colon and communicates to the genitourinary tract through a fistula. Diagnosis of CPC is usually made after birth when neonate/infant presents with abdominal distension and absence of anal opening. Making antenatal diagnosis of CPC is difficult because of the lack of specific and verifiable signs on sonography. Hence, only a few cases of antenatal diagnosis of CPC have been reported.1,2 In our case, CPC was suspected on a routine antenatal growth scan ultrasound in the late third trimester, showing a hypoechoic tubular-shaped lesion in the pre-sacral region. With this suspicion, we suggested an institutional delivery at a tertiary level centre, and diagnosis of type III CPC was confirmed on post-delivery imaging and…
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Taxonomy
TopicsCongenital gastrointestinal and neural anomalies · Gastrointestinal disorders and treatments · Intestinal Malrotation and Obstruction Disorders
