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Evaluation of Biomaterials for Bladder Augmentation using Cystometric Analyses in Various Rodent Models
Published on: August 9, 2012
Colorectal anomalies in patients with classic bladder exstrophy
Andrew A Stec1, Nima Baradaran, Christine Tran
1Division of Pediatric Urology, The Brady Urological Institute, The Johns Hopkins Medical Institutions, Baltimore, MD 21287, USA. andrew.stec@jhmi.edu
Insights
Children with classic bladder exstrophy (CBE) have a 1.8% rate of colorectal anomalies, primarily imperforate anus. Early evaluation and treatment are crucial for managing these significant associated conditions.
Area of Science:
- Pediatric Surgery
- Congenital Anomalies
- Urology
Background:
- Classic bladder exstrophy (CBE) is a complex congenital condition affecting the genitourinary system.
- Associated gastrointestinal malformations in CBE patients are not well-characterized.
- Understanding these comorbidities is vital for comprehensive patient care.
Purpose of the Study:
- To determine the incidence and types of colorectal anomalies in children with CBE.
- To assess the significance of these anomalies in the context of CBE.
Main Methods:
- Retrospective review of a database of 1044 patients with bladder exstrophy-epispadias-cloacal exstrophy complex.
- Detailed medical record review for 676 patients diagnosed with CBE.
- Identification and extraction of history for patients with gastrointestinal malformations.
Main Results:
- 12 out of 676 patients with CBE (1.8%) had a concomitant colorectal anomaly.
- Imperforate anus was the most common anomaly (8 patients).
- Other anomalies included severe rectal stenosis (2 patients) and congenital rectal prolapse (2 patients).
Conclusions:
- Isolated colorectal anomalies occur in 1.8% of children with CBE, a 72-fold increase over the general population.
- Despite being uncommon, these anomalies carry significant morbidity.
- Prompt evaluation and treatment of both genitourinary and colorectal issues are essential.
Aim:
This study aims to determine the proportion and type of colorectal anomalies that occur in children born with classic bladder exstrophy (CBE).
Methods:
All patients in a database of 1044 patients with the bladder exstrophy-epispadias-cloacal exstrophy complex were reviewed. Those with CBE had their complete medical records reviewed. Children noted to have gastrointestinal malformations were identified, and all aspects of their history were extracted.
Results:
A total of 676 patients were identified with CBE, of whom 12 patients were identified who had a concomitant colorectal anomaly. In this population, the proportion of colorectal anomalies is 1.8%. The most common gastrointestinal anomaly was imperforate anus in 8 patients. Two patients had severe rectal stenosis requiring serial dilations, and 2 patients were born with congenital rectal prolapse.
Conclusions:
Excluding all variants and cloacal patients with exstrophy, isolated colorectal anomalies occur at a rate of 1.8% in children born with CBE, a 72-fold increase compared with the general population. Although uncommon in this rare birth defect, the morbidity is significant and warrants prompt evaluation and treatment of both the genitourinary and colorectal anomalies.
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