Literature DB >> 17416075

[The Peutz-Jeghers syndrome--a case review].

M Skrovina1, S Czudek, J Bartos, I Ferák, L Adamcík, E Bezunková, R Vanko.   

Abstract

INTRODUCTION: The authors present a case review of a localized Peutz-Jeghers syndrome of the caecum, emulating a carcinoma.
METHODS: The patient who presented with insignificant family history with a diagnosed stenosing tumor of his appendix and histological findings of highly suspected adenocarcinoma, was indicated for surgical revision and right-sided hemicolectomy.
RESULTS: The patient underwent laparoscopically assissted right-sided hemicolectomy and his postoperative course was adequate. The final histological finding diagnosed solitary hamartoma of the Peutz-Jeghers polyp.
CONCLUSION: Differential diagnostic reasoning in patients with negative family history and unclear case history with findings of polypous tumorous lesions of the GIT, should also consider the Peutz-Jeghers syndrome. The syndrome is related to a high risk of malignancies in the elderly.

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Year:  2007        PMID: 17416075

Source DB:  PubMed          Journal:  Rozhl Chir        ISSN: 0035-9351


  1 in total

1.  Appendiceal cancer leading to intussusception detected incidentally during follow-up for Peutz-Jeghers syndrome.

Authors:  Kazuhiro Kurihara; Takanori Suganuma
Journal:  Clin J Gastroenterol       Date:  2020-10-09
  1 in total

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