Diclofenac-Induced Post Infantile Giant Cell Hepatitis

S. Venkataraman, V. Mohan, J. Conyers, Rukma Govindu
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引用次数: 1

Abstract

INTRODUCTION: Post-infantile Giant Cell Hepatitis (PIGCH) is a rare type of autoimmune hepatitis (AIH) characterized by an idiosyncratic response to liver injury from various causes in which liver cells respond to insult by rapid proliferation and without the appropriate cellular division, leading to the formation of the multi-nucleated giant cells. We encountered a case of Diclofenac induced PIGCH in a patient with untreated seropositive rheumatoid arthritis. To the best of our knowledge, this is first such case reported in the literature. CASE PRESENTATION: A 48-year-old Hispanic woman with type II diabetes and rheumatoid arthritis, not on DMARDs presented with acute onset jaundice and right upper quadrant pain. She was taking 50mg of Diclofenac, 2 pills daily for the past 3 months and unknown quantity of garlic tablets. Workup for hepatitis including infectious and toxic etiologies were ruled out. Serum IgG levels were elevated with increased globuin gap, and positive ANA titer of 640, anti-smooth muscle cell antibodies elevated at 41 units (moderate to strong positive > 30 units). Liver biopsy demonstrated submassive necrosis in the setting of post-infantile giant cell hepatitis. The differential diagnoses included idiopathic autoimmune hepatitis, viral or drug induced injury. Our diagnosis was drug induced autoimmune liver disease (DIALD), the etiology is likely due to Diclofenac given temporal relationship of drug intake and symptom onset, as well as a calculated Roussel Uclaf Causality Assessment Method (RUCAM) score of 6, signifying probable drug-induced liver disease. Patient was started on Prednisone and Azathioprine with complete resolution of clinical and laboratory findings within 5 months. DISCUSSION: The outcome of PIGCH is unpredictable, usually adopts a fulminant course leading to cirrhosis within months, however, a more benign course has also been described. PIGCH is triggered by three primary etiologies: drugs, infection, and autoimmune liver injury. This case highlights that giant cell hepatitis is a multifactorial condition that can be precipitated by drug use in the setting of autoimmune phenotype. Garlic and garlic extracts, through their antioxidant activities, have been reported to provide protection against free radical damage in the body. The innocuous course of PIGCH in our patient could possibly be due to concurrent consumption of garlic tablets. Further research is needed in this area.
双氯芬酸诱导的婴儿后巨细胞肝炎
简介:婴儿期后巨细胞肝炎(PIGCH)是一种罕见的自身免疫性肝炎(AIH),其特征是对各种原因引起的肝损伤有特殊反应,肝细胞通过快速增殖而没有适当的细胞分裂来对损伤做出反应,从而形成多核巨细胞。我们在一名未经治疗的血清阳性类风湿性关节炎患者中遇到了双氯芬酸诱导的PIGCH病例。据我们所知,这是文献中首次报道此类病例。病例介绍:一名48岁的西班牙裔女性,患有II型糖尿病和类风湿性关节炎,未服用DMARD,表现为急性发作性黄疸和右上象限疼痛。她服用了50毫克双氯芬酸,在过去的3个月里每天2粒,还有未知数量的大蒜片。排除了肝炎的治疗,包括传染性和毒性病因。血清IgG水平随着球蛋白间隙的增加而升高,ANA阳性滴度为640,抗平滑肌细胞抗体在41个单位时升高(中度至强阳性>30个单位)。肝活检显示在婴儿期后巨细胞肝炎的情况下出现亚大规模坏死。鉴别诊断包括特发性自身免疫性肝炎、病毒性或药物性损伤。我们的诊断是药物诱导的自身免疫性肝病(DIALD),病因可能是由于双氯芬酸,考虑到药物摄入和症状发作的时间关系,以及计算的Roussel-Uclaf因果关系评估方法(RUCAM)评分为6,表明可能是药物诱导性肝病。患者开始服用泼尼松和硫唑嘌呤,临床和实验室检查结果在5个月内完全消失。讨论:PIGCH的结果是不可预测的,通常会在几个月内出现导致肝硬化的暴发性过程,然而,也有人描述了一种更良性的过程。PIGCH由三种主要病因引发:药物、感染和自身免疫性肝损伤。该病例强调,巨细胞肝炎是一种多因素疾病,在自身免疫表型的情况下,药物使用可能会引发这种疾病。据报道,大蒜和大蒜提取物具有抗氧化活性,可以保护身体免受自由基损伤。我们患者的PIGCH无害过程可能是由于同时服用大蒜片所致。这方面还需要进一步的研究。
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