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Tunisie Medicale [La]. 2006; 84 (2): 128-130
em Francês | IMEMR | ID: emr-81438

RESUMO

Peutz-Jeghers syndrome is a hereditary affection with dominant autosomal transmission. The risk of cancerisation is largely higher than that in the general population. Dysplasia is rare. Transformation of the polyposis hamartoma into a site of dysplasia then into adenocarcinoma has been rarely reported. The authors report the case of a 14 year-old patient, having a severe dysplasia on ileal polyposis hamartoma related to the syndrome of Peutz-Jeghers


Assuntos
Humanos , Masculino , Família , Adenocarcinoma , Doenças Genéticas Inatas , Hamartoma
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