Anorectal malformations are a spectrum of conditions in which the anus, rectum, and sometimes the urinary and gynecologic structures do not form normally before birth. They range from a low malformation corrected in infancy to a cloaca, where the rectum, vagina, and urethra share a single channel and reconstruction is among the most demanding in all of pediatric surgery.
Repair restores the anatomy — most often through a posterior sagittal reconstruction — but the real goal is long-term function: bowel control, urinary control, and, later, healthy sexual and reproductive anatomy. That requires a surgeon who plans for the child’s whole future, not only the first operation.
How Dr. Calisto approaches it
- Full pelvic and anorectal reconstruction across the malformation spectrum, including cloaca
- Complex and redo reconstruction for children with poor results from a prior repair
- Published technique for rectovestibular fistula with vaginal agenesis, preserving the natural fecal reservoir
- Lifelong continence planning through a dedicated bowel-management program
A precise first reconstruction is the single best predictor of a continent child.