[Unusual complications of the Peutz-Jeghers-syndrome in two consecutive generations of the same family].

Abstract:

:The Peutz-Jeghers syndrome is an autosomal dominant inherited disease, characterized by the presence of hamartomatous polyposis of the gastrointestinal tract and perioral mucocutaneous pigmentation. The incidence of surgical complications in these patients is relatively rare, and correlates with the size and location of the polyps. We report on two complications of the Peutz-Jeghers syndrome which occurred in two generations of the same family. There was a perforation and an invagination of the small intestine. Both cases were treated by resection of the small intestine.

journal_name

Zentralbl Chir

authors

Lazaridis Ch,Papaziogas B,Atmatzidis K,Kalaitzis E,Pavlidis T,Papaziogas T

doi

10.1055/s-2002-22026

subject

Has Abstract

pub_date

2002-02-01 00:00:00

pages

147-50

issue

2

eissn

0044-409X

issn

1438-9592

journal_volume

127

pub_type

杂志文章
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