CZECH MEDICAL ASSOCIATION J. Ev. PURKYNĚ | |
Journals - Article | |
Česky / Czech version | Rozhl. Chir., 2007, roč. 86, č. 1, s. 24–26. |
The Peutz-Jeghers
Syndrom – A Case Review Škrovina M.1, Czudek S.1, Bartoš J.1, Ferák I.2, Adamčík L.1, Bezunková E.3, Vaňko R.1 1Chirurgické oddělení, Onkocentrum J. G. Mendela a Nemocnice Nový Jičín, primář: MUDr. S. Czudek, CSc. 2Patologie, P & R LAB s.r.o., Onkocentrum J. G. Mendela Nový Jičín, primář: MUDr. I. Ferák, Ph.D. 3Radiodiagnostické oddělení, Onkocentrum J. G. Mendela a Nemocnice Nový Jičín, primář: MUDr. M. Velkoborský |
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Summary: 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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