Juvenile polyposis syndrome

From Wikipedia, the free encyclopedia

Juvenile polyposis is a condition which presents when an individual is young hence it is called juvenile. The polyps are a growth that projects into the lumen like a mushroom, arising from the tissue underneath the epithelium layer (colonocytes).

The polyps can be solitary or multiple. If there are more than 5 polyps they are referred to as multiple. And if someone with juvenile polyps has more than 5 then the condition is referred to as Juvenile polyposis.

Contents

[edit] Presentation

They normally present at a young age with rectal bleeding which can be pretty concerning for the patient and parents. They can also present as a mass which has prolapsed outside the anus.

[edit] Pathophysiology

It is not clear if this condition has a genetic predisposition or if they are just sporadic. There has been some association with familial juvenile polyposis and the gene SMAD4 on chromosome 18 and PTEN on chromosome 10

[edit] Prognosis

Solitary polyps have no significant risk of cancer. But multiple polyps, polyposis syndrome, of the colon carry a 10% risk of developing into a cancer. This is mainly because of juvenile polyps developing adenomatous tissue.

[edit] Monitoring

If the patient has juvenile polyps they require yearly upper and lower endoscopies with the intention of excision and cytology.

[edit] Treatment

If you fear adenomatous tissue developing than you can offer surgery, namely colectomy and ileorectal anastomosis.

[edit] Screening

The siblings of patients with juvenile polyps can be screened, starting in their teens

[edit] External links