2012
DOI: 10.1200/jco.2011.39.7422
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[18F]Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography–Positive Gastric Adenocarcinoma in a 12-Year-Old Girl With Peutz-Jeghers Syndrome

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Cited by 4 publications
(2 citation statements)
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“…Peutz-Jeghers syndrome is a rare inherited autosomal dominant syndrome characterized by mucocutaneous pigmentations and diffuse gastrointestinal hamartomatous polyps. 2,3 Although hamartomatous polyps are generally assumed to have a low malignant potential, malignant transformation within the polyps has been observed in patients with Peutz-Jeghers syndrome. 4 It may be difficult to discriminate gastrointestinal polyps or adenomas from cancer on FDG PET because both can show increased FDG uptake.…”
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confidence: 99%
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“…Peutz-Jeghers syndrome is a rare inherited autosomal dominant syndrome characterized by mucocutaneous pigmentations and diffuse gastrointestinal hamartomatous polyps. 2,3 Although hamartomatous polyps are generally assumed to have a low malignant potential, malignant transformation within the polyps has been observed in patients with Peutz-Jeghers syndrome. 4 It may be difficult to discriminate gastrointestinal polyps or adenomas from cancer on FDG PET because both can show increased FDG uptake.…”
mentioning
confidence: 99%
“…Clear cell sarcoma was confirmed by pathology. Peutz-Jeghers syndrome is a rare inherited autosomal dominant syndrome characterized by mucocutaneous pigmentations and diffuse gastrointestinal hamartomatous polyps 2,3. Although hamartomatous polyps are generally assumed to have a low malignant potential, malignant transformation within the polyps has been observed in patients with Peutz-Jeghers syndrome 4.…”
mentioning
confidence: 99%