Simultaneous Presentation of Autoimmune Hepatitis and Wilson's Disease: A Systematic Review Study

IF 0.3 Q4 PEDIATRICS
Peiman Nasri, Seyed Esmaeil Hosseini-Kordkhyli, Azar Jafari-Koulaee, S. Hovsepian, H. Saneian, M. Khademian, F. Famouri
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Abstract

Background: The specialists should identify the features of Wilson disease and autoimmune hepatitis when both affect a patient to adopt appropriate treatment. Objectives: This study was conducted to determine features of the patient, disease, diagnostic studies, and therapeutic measures in cases of simultaneity of Wilson disease and autoimmune hepatitis. Methods: To find evidence related to the study objectives, we searched databases such as Barakat knowledge network system, SID, Magiran, Google Scholar, Web of Science, ProQuest, Springer, ScienceDirect, Medline via PubMed, and Scopus with specified Persian and English keywords, including “Wilson’s Disease”, “Autoimmune”, and “Hepatitis”. The inclusion criteria for the studies were 1) the study was observational and 2) the study was published in Persian or English. The exclusion criteria included low-quality studies based on the score obtained from the checklist. The obtained studies were screened in terms of titles, abstracts, and full text, and finally, the qualified studies entered the review process. The relevant data were extracted according to a designed checklist. Results: Finally, 10 studies were included in the review process. Information about 14 patients was reported. The Mean±SD age of the participants in the studies was 19±11 years. The direction of diagnosis was from autoimmune hepatitis to Wilson disease in 8 cases and from Wilson disease to autoimmune hepatitis in 3 cases. The simultaneity of autoimmune hepatitis and Wilson disease was considered in 3 patients with no primary and secondary diagnosis. Conclusions: The comorbidity of Wilson disease and autoimmune hepatitis is uncommon but is important. In the presence of relevant symptoms in these patients, the comorbidity of these two diseases should be considered. Accordingly, additional assessments such as serum ceruloplasmin, urinary 24-h copper, molecular genetic testing, MRI, serological tests, anti-nuclear antibody, anti-mitochondrial antibody, anti-smooth muscle antibody, complement level, gamma globulin, IgG, albumin, Kayser-Fleischer ring eye examination, and liver biopsy should be considered for correct diagnosis. If appropriate treatment was started for the disease with a diagnosis of Wilson disease or autoimmune hepatitis, but the response to treatment was insufficient, it is better to consider the simultaneous occurrence of two diseases or the initial misdiagnosis.
自身免疫性肝炎和Wilson病同时发病的系统回顾性研究
背景:当Wilson病和自身免疫性肝炎都影响患者时,专家应确定其特征,以采取适当的治疗方法。目的:本研究旨在确定威尔逊病和自身免疫性肝炎并发病例的患者特征、疾病、诊断研究和治疗措施。方法:为了寻找与研究目标相关的证据,我们搜索了Barakat知识网络系统、SID、Magiran、Google Scholar、Web of Science、ProQuest、Springer、ScienceDirect、Medline via PubMed和Scopus等数据库,并使用指定的波斯语和英语关键词,包括“Wilson’s Disease”、“Autoimmune”和“Hepatitics”。这些研究的纳入标准是:1)该研究是观察性的,2)该研究以波斯语或英语发表。排除标准包括基于检查表得分的低质量研究。对获得的研究进行了标题、摘要和全文筛选,最终,合格的研究进入审查程序。相关数据是根据设计的检查表提取的。结果:最后,10项研究被纳入审查过程。报告了14名患者的相关信息。研究参与者的平均±标准差年龄为19±11岁。诊断方向由自身免疫性肝炎转为Wilson病8例,由Wilson病转为自身免疫性肝3例。考虑了3例无一级和二级诊断的患者同时患有自身免疫性肝炎和Wilson病。结论:Wilson病和自身免疫性肝炎的合并症并不常见,但很重要。在这些患者出现相关症状的情况下,应考虑这两种疾病的合并症。因此,应考虑进行额外的评估,如血清铜蓝蛋白、尿液24小时铜、分子遗传学检测、MRI、血清学检测、抗核抗体、抗线粒体抗体、抗平滑肌抗体、补体水平、丙种球蛋白、IgG、白蛋白、Kayser-Flescher环眼检查和肝活检,以进行正确诊断。如果对诊断为Wilson病或自身免疫性肝炎的疾病开始了适当的治疗,但对治疗的反应不足,最好考虑两种疾病同时发生或最初的误诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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