Turcot Syndrome

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Turcot Syndrome This section has been reviewed and approved by the Cancer.Net Editorial Board [1], December / 2011 Overview What is Turcot syndrome? Turcot syndrome is a condition in which cells become abnormal and form masses called polyps. A polyp is benign (noncancerous) but can eventually turn malignant (cancerous, meaning it can spread to other parts of the body). Turcot syndrome is rare and is considered to be an alternative form of two more common syndromes associated with polyp formations: hereditary non-polyposis colorectal cancer [2] (HNPCC) and familial adenomatous polyposis [3] (FAP).

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A Challenging Treatment Decision for a Rare Association: Case Report of Familial Turcot Syndrome With Fistulizing Crohn’s Disease

Turcot syndrome and fistulizing Crohn’s disease (CD) are two disease entities that are not usually associated with one another, particularly given the rarity of the former. This is a case of a pediatric patient with fistulizing CD treated with biologic therapy, who was later found to have Turcot syndrome. Management of this rare combination of diseases can present several challenges, as surgica...

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[Turcot syndrome--a rare extra-intestinal manifestation of familial adenomatous polyposis?].

The case of a 15-year-old male with Turcot syndrome is presented. When the patient was aged 10 years a medulloblastoma was diagnosed. Five years later he developed multiple adenomatous polyps of the colon and multiple "congenital hypertrophy of the retina" (CHRPE), the most common extraintestinal manifestation of FAP, were described. Family history revealed familial adenomatous polyposis with 1...

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Case Reports: Pinealoblastoma in a Patient With Familial Adenomatous Polyposis: Variant of Turcot Syndrome Type 2? Report of a Case and Review of the Literature

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Turcot Syndrome: A Synchronous Clinical Presentation of Glioblastoma Multiforme and Adenocarcinoma of the Colon

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تاریخ انتشار 2012