Δημοσίευση

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

Τίτλος[Unusual complications of the Peutz-Jeghers-syndrome in two consecutive generations of the same family].
Publication TypeJournal Article
Year of Publication2002
AuthorsLazaridis, C., Papaziogas B., Atmatzidis K., Kalaitzis E., Pavlidis T., & Papaziogas T.
JournalZentralbl Chir
Volume127
Issue2
Pagination147-50
Date Published2002 Feb
ISSN0044-409X
Λέξεις κλειδιάAdult, Chromosome Aberrations, Female, Genes, Dominant, Humans, Intestinal Mucosa, Intestinal Neoplasms, Intestinal Perforation, Male, Peutz-Jeghers Syndrome, Polyps
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.

DOI10.1055/s-2002-22026
Alternate JournalZentralbl Chir
PubMed ID11894220

Επικοινωνία

Τμήμα Ιατρικής, Πανεπιστημιούπολη ΑΠΘ, T.K. 54124, Θεσσαλονίκη
 

Συνδεθείτε

Το τμήμα Ιατρικής στα κοινωνικά δίκτυα.
Ακολουθήστε μας ή συνδεθείτε μαζί μας.