Literature DB >> 2082804

[Peutz-Jeghers syndrome with carcinomatous degeneration of a duodenal hamartomatous polyp].

A Settaf1, F Mansori, S Bargach, A Saidi.   

Abstract

The authors report a case of Peutz-Jeghers syndrome in a young patient revealed by a duodenal carcinoma developed in a hamartomatous polyp. The absence of adenomatous lesion a the level of duodenal tumour, and the presence of hamartomatous lesions, particularly smooth muscular fibres, contiguous to carcinomatous glands, are favorable to a degenerescence of hamartomatous polyp. The question of malignant change or of the association of digestive carcinomas is discussed.

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Year:  1990        PMID: 2082804

Source DB:  PubMed          Journal:  Ann Gastroenterol Hepatol (Paris)        ISSN: 0066-2070


  3 in total

1.  Peutz-Jeghers polyps, dysplasia, and K-ras codon 12 mutations.

Authors:  M M Entius; A M Westerman; F M Giardiello; M L van Velthuysen; M M Polak; R J Slebos; J H Wilson; S R Hamilton; G J Offerhaus
Journal:  Gut       Date:  1997-09       Impact factor: 23.059

2.  Duodenal cancer in a young patient with Peuts-Jeghers syndrome harboring an entire deletion of the STK11 gene.

Authors:  Satoshi Teramae; Koichi Okamoto; Kumiko Tanaka; Reika Matsumoto; Shinji Kitamura; Tetsuo Kimura; Masahiro Sogabe; Hiroshi Miyamoto; Naoki Muguruma; Yoshimi Bando; Mitsuo Shimada; Tetsuji Takayama
Journal:  Clin J Gastroenterol       Date:  2017-03-16

Review 3.  [Peutz-Jeghers syndrome. Cases at the Mannheim clinic over 25 years].

Authors:  S Loff; L Wessel; H Wirth; B C Manegold; H Pilcher; K L Waag
Journal:  Langenbecks Arch Chir       Date:  1995
  3 in total

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