Peuz-Jeghers syndrome. New therapeutic approach endoscopic-surgical

Authors

  • Carlos Barberousse
  • Carlos Kierszembaun
  • Elena Trucco
  • Luis Carriquiry

Keywords:

digestive system, intestinal polyposis

Abstract

The Peutz-Jeghers Syndrome is a very
inrequent hereditary disorder. The main
characteristic is the association of intestinal
polyps and pigmented spots on lips and bucea!
mucous. lts natural history is about recurrent
attacks of co!icky abdominal pain due to
episodes of intestinal invagination. This results in
mu/tiple and acute laparotomies with
considerable morbidity and mortality which
final/y develop in a short bowel syndrome.
Recent studies have a/so determínate a greater
incidence of intestinal and extraintestinal cancer
in this patients.

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Published

2000-04-20

How to Cite

1.
Barberousse C, Kierszembaun C, Trucco E, Carriquiry L. Peuz-Jeghers syndrome. New therapeutic approach endoscopic-surgical. Cir. Urug. [Internet]. 2000 Apr. 20 [cited 2024 May 16];70(1-2):65-71. Available from: https://revista.scu.org.uy/index.php/cir_urug/article/view/4386

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Original Article

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