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Peutz-Jeghers syndrome--a rare case and a literature review.
Khirurgiia (Sofiia) ; (1): 43-8, 2014.
Article em Bg, En | MEDLINE | ID: mdl-25199243
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.
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Base de dados: MEDLINE Assunto principal: Síndrome de Peutz-Jeghers / Colonoscopia Tipo de estudo: Systematic_reviews Limite: Adult / Female / Humans Idioma: Bg / En Ano de publicação: 2014 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Síndrome de Peutz-Jeghers / Colonoscopia Tipo de estudo: Systematic_reviews Limite: Adult / Female / Humans Idioma: Bg / En Ano de publicação: 2014 Tipo de documento: Article