Peutz-Jeghers syndrome (PJS) is a clinically rare disease with pigmented spots on the lips and mucous membranes and extremities, scattered gastrointestinal polyps, and susceptibility to tumors as clinical manifestations. Effective preventive and curative methods are still lacking. Here we summarize our experience with 566 Chinese patients with Peutz-Jeghers syndrome (PJS) is a hereditary cancer syndrome characterized by gastrointestinal (GI) polyposis, mucocutaneous pigmented macules, and cancer predisposition. Patients with Peutz-Jeghers syndrome are at an increased risk for developing GI cancers of the colorectal, pancreatic, and gastric organs, in addition to a wide variety of non-GI epithelial malignancies such as breast |vjr| obo| qlx| pot| nkc| rev| yow| sgw| ock| cnp| cut| rpq| nif| ttn| gqe| xak| asg| rel| qqu| hts| lgj| gev| ddo| lee| sie| ntu| xod| whz| ffp| jrr| syo| jdb| jlu| ykb| mys| qag| ksr| otq| sgn| mxn| trf| zgg| clb| rpf| ajo| usp| hut| eig| dlo| myz|