| Literature DB >> 27540430 |
Yun Hee Kang1, Hye Kyung Lee2, Geon Park3.
Abstract
Cowden syndrome (CS) is a rare autosomal dominant disorder characterized by multiple hamartomas in various tissues and cancers (breast, thyroid, and endometrium). We report CS of the esophagus and gastrointestinal tract that was incidentally detected by positron emission tomography/computed tomography (PET/CT) at postoperative surveillance in an endometrial cancer patient. PET/CT showed mildly increased FDG uptake along the entire esophagus and stomach. Upper GI endoscopy and histologic examination revealed glycogenic acanthosis of the esophagus and several hundred gastric polyps. In our case, increased FDG uptake of the esophageal wall contributed to the diagnosis of CS.Entities:
Keywords: Cowden syndrome; Fluorodeoxyglucose F18; Hamartoma syndrome; Multiple; Positron emission tomography
Year: 2016 PMID: 27540430 PMCID: PMC4977259 DOI: 10.1007/s13139-016-0427-8
Source DB: PubMed Journal: Nucl Med Mol Imaging ISSN: 1869-3474