COLORECTAL NEOPLASIA IN PATIENTS WITH ULCERATIVE-COLITIS AND PRIMARY SCLEROSING CHOLANGITIS

Citation
Ak. Gurbuz et al., COLORECTAL NEOPLASIA IN PATIENTS WITH ULCERATIVE-COLITIS AND PRIMARY SCLEROSING CHOLANGITIS, Diseases of the colon & rectum, 38(1), 1995, pp. 37-41
Citations number
24
Categorie Soggetti
Gastroenterology & Hepatology
ISSN journal
00123706
Volume
38
Issue
1
Year of publication
1995
Pages
37 - 41
Database
ISI
SICI code
0012-3706(1995)38:1<37:CNIPWU>2.0.ZU;2-0
Abstract
PURPOSE: Most patients with primary sclerosing cholangitis also have u lcerative colitis. It has been suggested that in the presence of prima ry sclerosing cholangitis the risk of colorectal dysplasia and carcino ma is greater than in patients with ulcerative colitis alone. METHODS: In a retrospective study, we evaluated the possibility of colorectal cancer or dysplasia in 35 consecutive patients with primary sclerosing cholangitis and ulcerative colitis seen at The Johns Hopkins Hospital between 1979 and 1991. RESULTS: Thirteen of the 35 patients (37 perce nt) with ulcerative colitis and primary sclerosing cholangitis had col orectal neoplasia (5 with adenocarcinoma and 8 with dysplasia). In the 27 patients undergoing colonoscopic biopsy surveillance, the cumulati ve incidence at 28 years of colorectal cancer was 18.5 percent and for colorectal dysplasia it was 29.6 percent. The high incidence of color ectal cancer was less than the rate of colorectal cancer in patients w ith extensive colitis of childhood onset without primary sclerosing ch olangitis (35 percent), but the rate of colorectal cancer and dysplasi a (48.1 percent) is similar to the highest rates of cancer noted in th e comparison group. Because patients had subtle, quiescent colitis, a short time from diagnosis of ulcerative colitis to diagnosis of colore ctal neoplasia was noted (mean, 12.2 +/- 9 years; less than 8 years in 5/13 (38.5 percent) patients). CONCLUSION: Ulcerative colitis patient s with primary sclerosing cholangitis appear to have a high frequency of colorectal cancer but a rate lower than expected in patients with e xtensive quiescent ulcerative colitis of childhood onset alone. Howeve r, exact conclusions are complicated by the high incidence of colorect al dysplasia found, which portends malignant transformation. Because o f the subtle nature of colitis, the diagnosis of ulcerative colitis is often delayed, and surveillance programs should start as soon as ulce rative colitis is diagnosed.