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Conditions/Hereditary Cancers/Chapter

Detailed chapter

FAP (Familial Adenomatous Polyposis)

APC, heavy polyp burden, and surgical timing

Classic FAP is linked to germline APC changes and can produce hundreds to thousands of colorectal adenomas. Without planned care, colorectal cancer risk is very high. The path usually combines endoscopy, family history, and genetic counseling. It differs from Lynch mainly by polyp burden and gene pathway.

FAP · educational illustration

Key points

  • When to consider FAP
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    Young-onset numerous colon polyps, family polyposis/colectomy history, or selected extracolonic clues (for example desmoid disease or duodenal polyps) open evaluation.

  • Surgical frame
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    Risk-reducing colectomy timing and reconstruction options are planned with genetics, gastroenterology, and surgery together.

  • Family and follow-up
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    Pathogenic APC findings trigger cascade testing and structured endoscopic/surgical surveillance, including selected extracolonic risks.

  • Important
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    This page is for education. It is not medical advice and does not replace a visit with your physician.

Frequently asked questions

  • Is every multi-polyp colon FAP?
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    No. Attenuated FAP and MUTYH-associated polyposis (MAP) are discussed separately.

  • Is colectomy mandatory at diagnosis?
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    Timing and extent are individualized by polyp load, rectum status, and goals — not one package for everyone.

This page is for education. It is not medical advice and does not replace a visit with your physician.

Medical editor: Assoc. Prof. Cengiz Dibekoğlu, MD · Last medically reviewed: August 2026 · English patient-education chapter.