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原发性硬化性胆管炎与自身免疫性肝炎重叠综合征合并炎症性肠病:一例报告及系统评价

Primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome associated with inflammatory bowel disease: A case report and systematic review.

作者信息

Ballotin Vinícius Remus, Bigarella Lucas Goldmann, Riva Floriano, Onzi Georgia, Balbinot Raul Angelo, Balbinot Silvana Sartori, Soldera Jonathan

机构信息

Faculty of Medicine, Universidade de Caxias do Sul (UCS), Caxias do Sul 95070560, Brazil.

CPM Laboratório de Caxias do Sul, Caxias do Sul 95070561, Brazil.

出版信息

World J Clin Cases. 2020 Sep 26;8(18):4075-4093. doi: 10.12998/wjcc.v8.i18.4075.

Abstract

BACKGROUND

A previously healthy 22-year-old woman presented with abdominal pain and jaundice. She had a reagent antinuclear factor (1:640, with a homogeneous nuclear pattern) and hypergammaglobulinemia (2.16 g/dL). Anti-smooth muscle, anti-mitochondrial and anti-liver-kidney microsomal antibody type 1 antibodies were negative. Magnetic resonance cholangiography showed a cirrhotic liver with multiple focal areas of strictures of the intrahepatic bile ducts, with associated dilations. Liver biopsy demonstrated periportal necroinflammatory activity, plasmocyte infiltration and advanced fibrosis. Colonoscopy showed ulcerative pancolitis and mild activity (Mayo score 1), with a spared rectum. Treatment with corticosteroids, azathioprine, ursodeoxycholic acid and mesalamine was initiated, with improvement in laboratory tests. The patient was referred for a liver transplantation evaluation.

AIM

To report the case of a female patient with autoimmune hepatitis and primary sclerosing cholangitis (PSC) overlap syndrome associated with ulcerative colitis and to systematically review the available cases of autoimmune hepatitis and PSC overlap syndrome.

METHODS

In accordance with preferred reporting items for systematic reviews and meta-analysis protocols guidelines, retrieval of studies was based on medical subject headings and health sciences descriptors, which were combined using Boolean operators. Searches were run on the electronic databases Scopus, Web of Science, MEDLINE (PubMed), Biblioteca Regional de Medicina, Latin American and Caribbean Health Sciences Literature, Cochrane Library for Systematic Reviews and Opengray.eu. Languages were restricted to English, Spanish and Portuguese. There was no date of publication restrictions. The reference lists of the studies retrieved were searched manually.

RESULTS

The search strategy retrieved 3349 references. In the final analysis, 44 references were included, with a total of 109 cases reported. The most common clinical finding was jaundice and 43.5% of cases were associated with inflammatory bowel disease. Of these, 27.6% were cases of Crohn's disease, 68% of ulcerative colitis, and 6.4% of indeterminate colitis. Most patients were treated with steroids. All-cause mortality was 3.7%.

CONCLUSION

PSC and autoimmune hepatitis overlap syndrome is generally associated with inflammatory bowel disease and has low mortality and good response to treatment.

摘要

背景

一名既往健康的22岁女性出现腹痛和黄疸。她的抗核因子试剂检测结果为(1:640,核型均匀),且存在高球蛋白血症(2.16 g/dL)。抗平滑肌抗体、抗线粒体抗体和1型抗肝肾微粒体抗体均为阴性。磁共振胆胰管造影显示肝脏呈肝硬化,肝内胆管有多个局灶性狭窄区域,并伴有扩张。肝活检显示汇管区有坏死性炎症活动、浆细胞浸润及重度纤维化。结肠镜检查显示全结肠溃疡性炎症且活动度较轻(梅奥评分1分),直肠未受累。开始使用皮质类固醇、硫唑嘌呤、熊去氧胆酸和美沙拉嗪进行治疗,实验室检查结果有所改善。该患者被转诊进行肝移植评估。

目的

报告一名患有自身免疫性肝炎和原发性硬化性胆管炎(PSC)重叠综合征并伴有溃疡性结肠炎的女性患者病例,并系统回顾自身免疫性肝炎和PSC重叠综合征的现有病例。

方法

按照系统评价和Meta分析方案的首选报告项目指南,基于医学主题词和健康科学描述符检索研究,并使用布尔运算符进行组合。在电子数据库Scopus、科学网、MEDLINE(PubMed)、地区医学图书馆、拉丁美洲和加勒比健康科学文献、Cochrane系统评价图书馆和Opengray.eu上进行检索。语言限于英语、西班牙语和葡萄牙语。没有出版日期限制。对检索到的研究的参考文献列表进行手动检索。

结果

检索策略共获取3349篇参考文献。最终分析纳入44篇参考文献,共报告109例病例。最常见的临床发现是黄疸,43.5%的病例与炎症性肠病相关。其中,27.6%为克罗恩病病例,68%为溃疡性结肠炎病例,6.4%为不确定型结肠炎病例。大多数患者接受了类固醇治疗。全因死亡率为3.7%。

结论

PSC与自身免疫性肝炎重叠综合征通常与炎症性肠病相关,死亡率低,对治疗反应良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/7520795/d521293b368f/WJCC-8-4075-g001.jpg

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