Peutz-Jeghers syndrome--a rare case and a literature review

Maslyankov, S.; Trifonov, G.; Kyoseva, D.; Fidoshev, I.; Tzoneva, D.; Velev, G.; Dimova, I.; Sokolov, M.; Koleva, Q.; Todorov, G.; Maslyankov, S; Trifonov, G; Kyoseva, D; Fidoshev, I; Tzoneva, D; Velev, G; Dimova, I; Sokolov, M; Koleva, Q; Todorov, G

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Peutz-Jeghers syndrome--a rare case and a literature review

Maslyankov, S.; Trifonov, G.; Kyoseva, D.; Fidoshev, I.; Tzoneva, D.; Velev, G.; Dimova, I.; Sokolov, M.; Koleva, Q.; Todorov, G.

Khirurgiia 2014(1): 43-48

2014

ISSN/ISBN: 0450-2167

PMID: 25199243

Document Number: 676435

The Peutz-Jeghers syndrome is inherited condition, characterized by hamartomatous gastrointestinal polyposis and with mucocutaneous pigmentation. We have experienced a case with typical clinical features, diagnosed before complication's development. In order to prevent cancer setting it is recommended to perform aggressive screening and high-technological procedures.