Cancer risk and mortality in patients with solitary Peutz-Jeghers polyps
Anne Marie Jelsig1
Laus Wullum2
Lilian Bomme Ousager3
Johan Burish4
Tine Plato Kühlmann5
John Gásdal Karstensen6
1.Department of Clinical Genetics,University Hospital of Copenhagen,Rigshospitalet,Copenhagen,Denmark2.Omicron Aps,Copenhagen,Denmark3.Department of Clinical Genetics,Odense University Hospital,Odense,Denmark;Human Genetics,Institute of Clinical Research,University of Southern Denmark,Odense,Denmark4.Gastrounit,Medical Division,Copenhagen University Hospital—Amager and Hvidovre,Hvidovre,Denmark5.Department of Pathology,Copenhagen University Hospital,Herlev,Denmark;Department of Clinical Medicine,University of Copenhagen,Copenhagen,Denmark6.Department of Clinical Medicine,University of Copenhagen,Copenhagen,Denmark;Danish Polyposis Registry,Gastrounit,Copenhagen University Hospital—Amager and Hvidovre,Hvidovre,Denmark
摘要：Introduction
Solitary Peutz-Jeghers polyps are hamartomatous lesions in the gastrointestinal(GI)tract.They are rare and can be diagnosed in both children and adults(Figure 1A).Microscopically,Peutz-Jeghers polyps can have a characteristic morphology,making it possible to distinguish them from other polyps(Figure 1B and C).
机标关键词：peutz-jegherscancerriskwithmortalitypatientspolypssolitary
论文发表日期：2024-06-30
在线出版日期：2026-07-17（本平台首次上网日期，不代表文献的发表时间）
页数：3( 290-292 )