RESUMEN
Peutz Jeghers Syndrome [PJS], which was first described in 1921 by Peutz1, followed by Jeghers etal in 19492, is an uncommon but not a rare disorder characterized by mucocutaneous melanin pigmentation, gastrointestinal hamartomatous polyps and increased risk of gastrointestinal and other organs cancer 1, 3, 4.The polyps vary in size from few millimeters to several centimeters, with lobulated surface, and could be pedunculated as in large polyps, or sessile as in the small ones5.The clinical symptoms of the disease are recurrent abdominal pain, intestinal intussusception and obstruction, gastrointestinal bleeding with symptoms of iron deficiency anaemia. The symptoms usually take place in the second and third decade of life6.The complications of PJS which brings the patient to the doctor is severe anemia due to blood loss from GIT, acute abdomen, intestinal obstruction due to tumor-mass obstruction or intussusception, or rarely due to gastric outlet obstruction as in this presented case7.The treatment of polyposis is by endoscopic polypectomy, laprotomy and resection which may lead to complications as short bowel syndrome. The other difficulty which the doctor comes across while managing these cases is to follow-up the occurrence of malignant disease in these patients, malignant changes of hamartomatus polyps and other organs cancers have been reported in patients with PJS8