• Arch Med Sci · Apr 2010

    Case Reports

    Colorectal cancer in the course of familial adenomatous polyposis syndrome ("de novo" pathogenic mutation of APC gene): case report, review of the literature and genetic commentary.

    • Rafał Stec, Andrzej Pławski, Agnieszka Synowiec, Michał Mączewski, and Cezary Szczylik.
    • Department of Oncology, Military Institute of Medicine, Warsaw, Poland.
    • Arch Med Sci. 2010 Apr 30; 6 (2): 283287283-7.

    AbstractColorectal cancer (CRC) is one of the most common malignant tumours in Poland. Annually approximately 11 000 new cases of CRC are diagnosed, while the number of deaths caused by CRC approaches 8 000. Five-year survival does not exceed 20%. Familial adenomatous polyposis (FAP) is responsible for about 1% of new cases of CRC. The risk of CRC in FAP syndrome is 100%, and the average age of CRC development is 39 years. Early colectomy is the most effective method of CRC prevention. We report an atypical case of CRC in a patient with FAP caused by 2797-2800delAACA mutation of the APC gene.

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