Clinical Analysis Of Peutz-Jeghers Syndrome: A Report Of 3 Cases

Objective:To investigate the Peutz-Jeghers syndrome (PJS) clinical features, diagnosis and treatment.Methods:Retrospective analysis of our hospitals the past two years 3 cases were treated syndrome in PJS.Results:All 3 patients had gastrointestinal polyps and mucocutaneous pigmented skin,1 patients with family history. Clinical manifestations:abdominal pain, melena.3 patients underwent endoscopic treatment for many times.Conclusion:PJS is autosomal dominant syndrome, easily complicated by intestinal obstruction, intussusception, alimentary tract hemorrhage. Endoscopic therapy is the preferred treatment. PJS patients are often cancerous,so surveillance should be emphasized.