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克罗恩病患者的肝胆功能障碍与原发性硬化性胆管炎

Hepatobiliary dysfunction and primary sclerosing cholangitis in patients with Crohn's disease.

作者信息

Rasmussen H H, Fallingborg J F, Mortensen P B, Vyberg M, Tage-Jensen U, Rasmussen S N

机构信息

Dept. of Medical Gastroenterology, Aalborg Hospital, Denmark.

出版信息

Scand J Gastroenterol. 1997 Jun;32(6):604-10. doi: 10.3109/00365529709025107.

Abstract

BACKGROUND

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.

METHODS

Patients with CD and long-standing abnormal liver function results were investigated individually with endoscopic retrograde cholangiography and liver biopsy.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

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