Severe Acute Liver Injury due to Secondary Hemophagocytic Lymphohistiocytosis: A Case Report.

IF 1 Q4 GASTROENTEROLOGY & HEPATOLOGY
GE Portuguese Journal of Gastroenterology Pub Date : 2023-03-30 eCollection Date: 2023-11-01 DOI:10.1159/000529549
Cristiana Sequeira, Sara Ramos Lopes, Anabela Neves, Inês Costa Santos, Cláudio Rodrigues Martins, Ana Paula Oliveira
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引用次数: 0

Abstract

Severe acute liver injury (ALI) is mostly triggered by viral infections and hepatotoxic drugs; however, it can also be seen in systemic diseases. Hemophagocytic lymphohistiocytosis (HLH) is a rare, immune-mediated syndrome that presents as a life-threatening inflammatory disorder affecting multiple organs. Secondary causes occur mainly in the set of malignancy, infection, and autoimmune disease, and are seldom triggered by vaccination. Although liver involvement is common, presentation as severe ALI is rare. We describe a case of a 65-year-old male with history of low-risk chronic lymphocytic leukemia and rheumatoid arthritis treated with prednisolone who presented with persistent fever and jaundice 1 week after COVID-19 vaccination. The diagnosis was challenging given the predominant liver impairment, characterized by hyperbilirubinemia, transaminases over 1,000 U/L, and prolonged INR, which prompted an extensive investigation and exclusion of autoimmune, toxic, and viral causes of hepatitis. Laboratory workup revealed bicytopenia, hyperferritinemia, which together with organ failure and evidence of hemophagocytosis in bone marrow suggested the diagnosis of HLH. After excluding infectious etiologies, flare of rheumatological disease, and the progression of hematological disease, HLH was diagnosed. He was successfully treated with etoposide and corticosteroids, with dramatic improvement of liver tests. After exclusion of other causes of secondary HLH, the recent vaccination for COVID-19 was the likely trigger. We report a case of double rarity of HLH, as it presented with severe liver dysfunction which was probably triggered by vaccination. In this case, the predominant liver involvement urged extensive investigation of liver disease, so a high index of suspicion was required to make an early diagnosis. Clinicians should consider HLH in patients with unexplained signs and symptoms of systemic inflammatory response and multiorgan involvement, including severe liver involvement as the first presentation.

继发性噬血细胞性淋巴组织细胞病致严重急性肝损伤1例报告。
严重急性肝损伤(ALI)多由病毒感染和肝毒性药物引起;然而,它也见于全身性疾病。噬血细胞性淋巴组织细胞增多症(HLH)是一种罕见的免疫介导的综合征,是一种危及生命的炎症性疾病,影响多个器官。继发原因主要发生在恶性肿瘤、感染和自身免疫性疾病,很少由接种引起。虽然累及肝脏是常见的,但表现为严重ALI是罕见的。我们描述了一例65岁男性,患有低风险慢性淋巴细胞白血病和类风湿关节炎病史,接受强的松龙治疗,在接种COVID-19疫苗1周后出现持续发热和黄疸。考虑到以高胆红素血症、转氨酶超过1000 U/L和INR延长为特征的主要肝功能损害,诊断是具有挑战性的,这促使了广泛的调查和排除自身免疫性、毒性和病毒性肝炎原因。实验室检查显示双氧体减少症,高铁蛋白血症,并伴有器官衰竭和骨髓噬血症,提示诊断为HLH。排除感染性病因、风湿病发作和血液病进展后,诊断为HLH。他成功地接受了依托泊苷和皮质类固醇治疗,肝脏检查有了显著改善。在排除了继发性HLH的其他原因后,最近接种的COVID-19疫苗可能是触发因素。我们报告一个病例的双重罕见的HLH,因为它提出了严重的肝功能障碍,这可能是由疫苗接种引发的。在这个病例中,主要的肝脏受累需要广泛的肝脏疾病调查,因此需要高度的怀疑指数来做出早期诊断。临床医生应考虑出现全身性炎症反应和多器官受累(包括以严重肝脏受累为首发表现)的不明体征和症状的患者。
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来源期刊
GE Portuguese Journal of Gastroenterology
GE Portuguese Journal of Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
1.60
自引率
11.10%
发文量
62
审稿时长
21 weeks
期刊介绍: The ''GE Portuguese Journal of Gastroenterology'' (formerly Jornal Português de Gastrenterologia), founded in 1994, is the official publication of Sociedade Portuguesa de Gastrenterologia (Portuguese Society of Gastroenterology), Sociedade Portuguesa de Endoscopia Digestiva (Portuguese Society of Digestive Endoscopy) and Associação Portuguesa para o Estudo do Fígado (Portuguese Association for the Study of the Liver). The journal publishes clinical and basic research articles on Gastroenterology, Digestive Endoscopy, Hepatology and related topics. Review articles, clinical case studies, images, letters to the editor and other articles such as recommendations or papers on gastroenterology clinical practice are also considered. Only articles written in English are accepted.
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