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儿童自身免疫性硬化性胆管炎:一项前瞻性病例对照研究。

Autoimmune Sclerosing Cholangitis in Children: A Prospective Case-Control Study.

作者信息

Kumar Nagendra, Poddar Ujjal, Yadav Rajnikant, Lal Hira, Pani Krushna, Yachha Surender Kumar, Srivastava Anshu, Pandey Rakesh

机构信息

Department of Pediatric Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.

Department of Radiodiagnosis, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.

出版信息

Pediatr Gastroenterol Hepatol Nutr. 2021 Mar;24(2):154-163. doi: 10.5223/pghn.2021.24.2.154. Epub 2021 Mar 8.

Abstract

PURPOSE

In children overlap of autoimmune hepatitis (AIH) and primary sclerosing cholangitis is labelled as autoimmune sclerosing cholangitis (ASC). The only prospective pediatric study showed a high prevalence of ASC by using endoscopic retrograde cholangiopancreatography. Aims of our study were to find the prevalence of ASC by using magnetic resonance cholangiography (MRC) in AIH and in non-AIH cirrhosis and to compare clinical presentation and outcome of AIH and ASC.

METHODS

Prospectively we did MRC in 38 children with AIH (cases) and 19 disease controls (Wilson disease). Multiple biliary strictures with proximal dilatation on MRC were taken as definitive changes of ASC. Detail clinical, laboratory parameters, liver histopathology and treatment outcome were recorded.

RESULTS

The median age of cases was 11.5 (3-18) years, 22 (57.9%) were girls and 28 (73.7%) were diagnosed as type 1 AIH. MRC was done in 11 children (28.9%) at the time of diagnosis and in 27 (71.1%) after a median follow-up of 2.5 (0.3-10) years. Abnormal MRC changes were seen in 14/38 (36.8%) of AIH and 8/19 (42.1%) of controls. However, definite changes of ASC were present in four (10.5%) children in AIH and none in controls. None of the clinical, laboratory, histological parameters and treatment response were significantly different between ASC and AIH groups.

CONCLUSION

The prevalence of ASC in children with AIH was just 10.5%. We suggest MRC in select group with cholestatic features, inflammatory bowel disease and in those who showed poor response to immunosuppression instead of all children with AIH.

摘要

目的

在儿童中,自身免疫性肝炎(AIH)与原发性硬化性胆管炎的重叠被标记为自身免疫性硬化性胆管炎(ASC)。唯一一项前瞻性儿科研究显示,通过内镜逆行胰胆管造影术,ASC的患病率很高。我们研究的目的是通过磁共振胆管造影(MRC)来确定AIH和非AIH肝硬化患儿中ASC的患病率,并比较AIH和ASC的临床表现及转归。

方法

我们前瞻性地对38例AIH患儿(病例组)和19例疾病对照(威尔逊病)进行了MRC检查。MRC显示的多发胆管狭窄伴近端扩张被视为ASC的确诊改变。记录详细的临床、实验室参数、肝脏组织病理学及治疗结果。

结果

病例组的中位年龄为11.5(3 - 18)岁,22例(57.9%)为女孩,28例(73.7%)被诊断为1型AIH。11例患儿(28.9%)在诊断时进行了MRC检查,27例(71.1%)在中位随访2.5(0.3 - 10)年后进行了MRC检查。38例AIH患儿中有14例(36.8%)MRC检查结果异常,19例对照中有8例(42.1%)异常。然而,AIH患儿中有4例(10.5%)出现了ASC的确诊改变,对照组中无确诊病例。ASC组和AIH组在临床、实验室、组织学参数及治疗反应方面均无显著差异。

结论

AIH患儿中ASC的患病率仅为10.5%。我们建议,对于有胆汁淤积特征、炎症性肠病以及对免疫抑制治疗反应不佳的特定患儿群体,而非所有AIH患儿,进行MRC检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8953/8007839/2f4e5fbce907/pghn-24-154-g001.jpg

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