Rasmussen H H, Fallingborg J F, Mortensen P B, Vyberg M, Tage-Jensen U, Rasmussen S N
Dept. of Medical Gastroenterology, Aalborg Hospital, Denmark.
Scand J Gastroenterol. 1997 Jun;32(6):604-10. doi: 10.3109/00365529709025107.
Only a few studies have attempted to determined the prevalence of long-standing abnormal liver function and primary sclerosing cholangitis (PSC) in patients with Crohn's disease (CD). The aim of the study was to determine the prevalence of long-standing abnormal liver function test results and to describe the clinical, biochemical, and histologic findings in patients with large-duct classic PSC and small-duct PSC (that is, normal cholangiogram) in patients with CD during a 15-year period.
Patients with CD and long-standing abnormal liver function results were investigated individually with endoscopic retrograde cholangiography and liver biopsy.
Of 262 consecutive patients with CD, 38 (15%) had long-standing increased alkaline phosphatase (ALP) values (mean, 1065 U/l; range, 321-4165 U/l). Of these, 10 patients were classified as having hepatic disease (4%), of which 9 had PSC and 1 had a non-specific reactive hepatitis. Of nine patients with PSC (3.4%), three were classified as having large-duct PSC; five, small-duct PSC; and one, unclassified. In patients with large-bowel CD (n = 102) the prevalence of PSC was 9%. Mean age at diagnosis of PSC was 35 years (22-46 years), and the female to male ratio, 7:2. All PSC patients had large-bowel involvement (P < 0.00015), and two of them developed colonic carcinoma of the large bowel (P < 0.01). All cases of small-duct PSC were stage 1, whereas large-duct PSC were stage 2-3. During the observation period (mean, 5.4 years) no PSC patients died.
The results of our study indicate that PSC is the major hepatic disease in patients with CD and long-standing abnormal liver function tests and is approximately as prevalent as in ulcerative colitis. Patients with PSC and CD may have a milder liver disease than patients with PSC and ulcerative colitis, perhaps because large-duct PSC is less common in patients with CD. Cholangiograms and liver biopsies are both needed to evaluate the extent of the disease.
仅有少数研究试图确定克罗恩病(CD)患者中长期存在的肝功能异常及原发性硬化性胆管炎(PSC)的患病率。本研究的目的是确定长期肝功能检查结果异常的患病率,并描述15年间CD患者中具有大胆管典型PSC及小胆管PSC(即胆管造影正常)患者的临床、生化及组织学表现。
对CD及长期肝功能结果异常的患者分别进行内镜逆行胆管造影及肝活检。
在262例连续的CD患者中,38例(15%)长期碱性磷酸酶(ALP)值升高(平均1065 U/l;范围321 - 4165 U/l)。其中,10例患者被归类为患有肝病(4%),其中9例患有PSC,1例患有非特异性反应性肝炎。在9例PSC患者(3.4%)中,3例被归类为大胆管PSC;5例为小胆管PSC;1例未分类。在大肠CD患者(n = 102)中,PSC的患病率为9%。PSC诊断时的平均年龄为35岁(22 - 46岁),女性与男性比例为7:2。所有PSC患者均有大肠受累(P < 0.00015),其中2例发生了大肠癌(P < 0.01)。所有小胆管PSC病例均为1期,而大胆管PSC为2 - 3期。在观察期(平均5.4年)内,无PSC患者死亡。
我们的研究结果表明,PSC是CD及长期肝功能检查异常患者中的主要肝脏疾病,其患病率与溃疡性结肠炎大致相同。与PSC合并溃疡性结肠炎的患者相比,PSC合并CD的患者肝脏疾病可能较轻,这可能是因为大胆管PSC在CD患者中较少见。胆管造影和肝活检均需要用于评估疾病的程度。