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Gardner syndrome, also known as familial colorectal polyposis, is an autosomal dominant disease and is part of the spectrum\udof familial adenomatous polyposis (FAP) syndromes. It is characterized by the presence of multiple polyps in the colon\udtogether with neoplasms outside the colon. Gardner syndrome is also associated with desmoid tumors in approximately\ud15% of affected individuals. Desmoid tumors are rare benign slow-growing neoplasms, arising from connective tissue\ud(musculoaponeurotic fibrous tissue). Due to their locally aggressive nature, the term aggressive fibromatosis have been\udused to describe these tumors. Seven percent of patients with FAP or its variants may also have adrenal masses, most being\udbenign and asymptomatic. We report the PET/CT of a 42 year old patient who was diagnosed with Gardner syndrome,\uddemonstrating the rare coexistence of the intestinal polyps, extra and intra-abdominal desmoids and adrenal adenoma by\udPET/CT. In addition, the characteristic cutaneous lesions and osteomas of the skull were also identified

Gardner Syndrome with Extra and Intra-Abdominal Desmoid Tumors and Adrenal Involvement: PET/CT Findings