PT - JOURNAL ARTICLE AU - R Scheenstra AU - F E M Rijcken AU - J J Koornstra AU - H Hollema AU - R Fodde AU - F H Menko AU - R H Sijmons AU - C M A Bijleveld AU - J H Kleibeuker TI - Rapidly progressive adenomatous polyposis in a patient with germline mutations in both the <em>APC</em> and <em>MLH1</em> genes: the worst of two worlds AID - 10.1136/gut.52.6.898 DP - 2003 Jun 01 TA - Gut PG - 898--899 VI - 52 IP - 6 4099 - http://gut.bmj.com/content/52/6/898.short 4100 - http://gut.bmj.com/content/52/6/898.full SO - Gut2003 Jun 01; 52 AB - The two most common inherited forms of colorectal cancer are familial adenomatous polyposis and hereditary non-polyposis colorectal cancer. Simultaneous inheritance of both an APC gene mutation and a mismatch repair gene (for example, MLH1) mutation has never been described. In the present case report, we report rapidly progressive adenomatous polyposis in a 10 year old boy with a germline frame shift mutation in the APC gene and a germline splice site mutation in the MLH1 gene. Immunohistochemical investigations showed abnormal expression of β-catenin in early adenomas with low grade dysplasia, attributed to the APC gene mutation. Subsequent loss of function of the MLH1 gene, as shown by absent immunostaining of its protein in adenomas with high grade dysplasia, may well have caused the rapid progression to high grade dysplasia in many of the adenomas.