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Gardner Syndrome with Extra and Intra-Abdominal Desmoid Tumors and Adrenal Involvement: PET/CT Findings
Author(s) -
Alshaima Alshammari,
Rasha Ashkanani,
Saker Alabsi,
Mohammed Ghanem
Publication year - 2015
Publication title -
molecular imaging and radionuclide therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.292
H-Index - 7
eISSN - 2147-1959
pISSN - 2146-1414
DOI - 10.4274/mirt.57966
Subject(s) - medicine , gardner's syndrome , radiology , nuclear medicine , pathology
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

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