Abstract

G A A b st ra ct s disease rather than cancer/dysplasia (88% vs 29%; p=0.02). In contrast, surgical indication did not influence chronic pouch inflammation among -PSC (26% vs 18%, p=0.38).Conclusions: +PSC have unique clinical and serologic characteristics that distinguish them from -PSC. +PSC patients who undergo IPAA for refractory disease rather than dysplasia are more likely to develop chronic pouch inflammation. Validation of these findings in a larger cohort is warranted.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call