This report examines a 17-year-old female with familial adenomatous polyposis, revealing increased colorectal cancer risk and treatment outcomes.
Familial adenomatous polyposis (FAP) is a rare disease syndrome characterized by mutations in the Adenomatous Polyposis Coli gene. Affected people have a markedly increased lifetime risk of colorectal cancer. The patient was a 17-year-old female with a 4- year history of intermittent abdominal pain, rectal bleeding, and anal masses. A proctocolectomy with perineal resection and a permanent ileostomy were performed. The histological findings were consistent with that of FAP. FAP can present in young patients with rectal bleeding and anal masses
No takes yet. Share an insight, caveat, or question.
Bokalli et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: