Filiation Hamartoma polyposis dysplasia and small bowel adeno-carcinoma
Tunisie Medicale [La]. 2006; 84 (2): 128-130
em Francês
| IMEMR
| ID: emr-81438
ABSTRACT
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
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Adenocarcinoma
/
Família
/
Hamartoma
/
Doenças Genéticas Inatas
Tipo de estudo:
Relato de Casos
Limite:
Humanos
/
Masculino
Idioma:
Francês
Revista:
Tunisie Med.
Ano de publicação:
2006
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