Juvenile polyposis: Focus on less described manifestations

Elsevier

Available online 4 August 2022, 101802

Best Practice & Research Clinical GastroenterologyAbstract

Juvenile polyposis represents an heterogeneous disease as different genetic dominant backgrounds have been evidenced leading to different clinical presentations. It is associated in some patients with a different syndrome, Hereditary Hemorragic Telangiectasia, justifying a complementary and different management. Recent international recommendations help in managing this very rare disease, and this management should probably be restricted to expert centers able to take care of the multiple manifestations and risks of these patients and families. This paper will focus on the poorly known and evaluated aspects of juvenile polyposis, excluding the colonic involvement and epidemiology that are addressed in a different article of this issue.

Keywords

Polyposis

Juvenile

Cancer

Hereditary haemorragic telangiectasia

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