Genotype–phenotype correlation for extracolonic aggressive phenotypes in patients with familial adenomatous polyposis

Abstract

Familial adenomatous polyposis (FAP) patients develop various life‐threatening extracolonic comorbidities that appear individually or within a family. This diversity can be explained by the localization of the adenomatous polyposis coli (APC) variant, but few reports provide definitive findings about genotype–phenotype correlations. Therefore, we investigated FAP patients and the association between the severe phenotypes and APC variants. Of 247 FAP patients, 126 patients from 85 families identified to have APC germline variant sites were extracted. These sites were divided into six groups (Regions A to F), and the frequency of severe comorbidities was compared among the patient phenotypes. Of the 126 patients, the proportions of patients with desmoid tumor stage ≥III, number of FGPs ≥1000, multiple gastric neoplasms, gastric neoplasm with high‐grade dysplasia, and Spigelman stage ≥III were 3%, 16%, 21%, 12%, and 41%, respectively, while the corresponding rates were 30%, 50%, 70%, 50%, and 80% in patients with Region E (codons 1398–1580) variants. These latter rates were significantly higher than those for patients with variants in other regions. Moreover, the proportion of patients with all three indicators (desmoid tumor stage ≥III, number of FGPs ≥1000, and Spigelman stage ≥III) was 20% for those with variants in Region E and 0% for those with variants in other regions. Variants in Region E indicate aggressive phenotypes, and more intensive management is required.

Dual primary gastric and colorectal cancer: The known hereditary causes and underlying mechanisms

“…Most patients have a family history of colorectal polyps and cancer. Patients may present with extraintestinal manifestations, individually or in the family, including osteomas, unerupted teeth, congenital absence of teeth, desmoid tumours[ 10 ], and extracolonic cancers (thyroid, liver, bile ducts, duodenum, and central nervous system). It results from a germline mutation in the adenomatous polyposis ( APC ) gene.…”