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Title: Cowden's syndrome with Lhermitte-Duclos disease. Author: Boonpipattanapong T, Phuenpathom N, Mitarnun W. Journal: Br J Neurosurg; 2005 Aug; 19(4):361-5. PubMed ID: 16455548. Abstract: Cowden's syndrome (CS) is a rare autosomal dominant condition featuring multiple hamartomas, often with mucocutaneous lesions, goitre, breast cancer, gastrointestinal polyps or even Lhermitte-Duclos disease (LDD). In this article we report the case of a 34-year-old man who was diagnosed with LDD. Subsequent examinations also revealed manifestations of CS, i.e. macrocephaly, thyroid nodules and gastrointestinal polyps.[Abstract] [Full Text] [Related] [New Search]