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高效抗逆转录病毒治疗期间的人类免疫缺陷病毒感染与自身免疫性肝炎:一例病例报告及文献综述

Human immunodeficiency virus infection and autoimmune hepatitis during highly active anti-retroviral treatment: a case report and review of the literature.

作者信息

Daas Hanady, Khatib Riad, Nasser Haitham, Kamran Farah, Higgins Martha, Saravolatz Louis

机构信息

Department of Internal Medicine, Division of Infectious Diseases, St John Hospital & Medical Center, 19251 Mack Avenue, Suite 340, Grosse Pointe Woods, MI 48236, USA.

出版信息

J Med Case Rep. 2011 Jun 25;5:233. doi: 10.1186/1752-1947-5-233.

DOI:10.1186/1752-1947-5-233
PMID:21702972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3141694/
Abstract

INTRODUCTION

The emergence of hepatic injury in patients with human immunodeficiency virus infection during highly active therapy presents a diagnostic dilemma. It may represent treatment side effects or autoimmune disorders, such as autoimmune hepatitis, emerging during immune restoration.

CASE PRESENTATION

We present the case of a 42-year-old African-American woman with human immunodeficiency virus infection who presented to our emergency department with severe abdominal pain and was found to have autoimmune hepatitis. A review of the literature revealed 12 reported cases of autoimmune hepatitis in adults with human immunodeficiency virus infection, only three of whom were diagnosed after highly active anti-retroviral treatment was initiated. All four cases (including our patient) were women, and one had a history of other autoimmune disorders. In our patient (the one patient case we are reporting), a liver biopsy revealed interface hepatitis, necrosis with lymphocytes and plasma cell infiltrates and variable degrees of fibrosis. All four cases required treatment with corticosteroids and/or other immune modulating agents and responded well.

CONCLUSION

Our review suggests that autoimmune hepatitis is a rare disorder which usually develops in women about six to eight months after commencing highly active anti-retroviral treatment during the recovery of CD4 lymphocytes. It represents either re-emergence of a pre-existing condition that was unrecognized or a de novo manifestation during immune reconstitution.

摘要

引言

在高效抗逆转录病毒治疗期间,人类免疫缺陷病毒感染患者出现肝损伤会带来诊断难题。这可能代表治疗副作用或自身免疫性疾病,如免疫重建过程中出现的自身免疫性肝炎。

病例报告

我们报告一例42岁的非裔美国女性人类免疫缺陷病毒感染患者,她因严重腹痛就诊于我院急诊科,被诊断为自身免疫性肝炎。文献回顾显示,有12例成人人类免疫缺陷病毒感染合并自身免疫性肝炎的报告病例,其中仅3例是在开始高效抗逆转录病毒治疗后确诊的。所有4例病例(包括我们的患者)均为女性,且1例有其他自身免疫性疾病史。在我们的患者(我们报告的这例单一病例)中,肝活检显示界面性肝炎、淋巴细胞和浆细胞浸润伴坏死以及不同程度的纤维化。所有4例病例均需要用皮质类固醇和/或其他免疫调节剂治疗,且反应良好。

结论

我们的回顾表明,自身免疫性肝炎是一种罕见疾病,通常在女性开始高效抗逆转录病毒治疗后约6至8个月、CD4淋巴细胞恢复过程中发生。它代表既往未被识别的疾病复发或免疫重建过程中的新发表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644c/3141694/9c89a70c0fad/1752-1947-5-233-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644c/3141694/43920de7f799/1752-1947-5-233-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644c/3141694/9c89a70c0fad/1752-1947-5-233-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644c/3141694/43920de7f799/1752-1947-5-233-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644c/3141694/9c89a70c0fad/1752-1947-5-233-2.jpg

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