Giant cell hepatitis associated with autoimmune hemolytic anemia: an update.

IF 3 4区 医学 Q1 Medicine
Translational gastroenterology and hepatology Pub Date : 2021-04-05 eCollection Date: 2021-01-01 DOI:10.21037/tgh.2020.03.10
Silvia Nastasio, Lorenza Matarazzo, Marco Sciveres, Giuseppe Maggiore
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引用次数: 3

Abstract

Giant cell hepatitis associated with autoimmune hemolytic anemia (GCH-AHA) is a rare and severe disease characterized by autoimmune hemolysis associated with acute liver injury, histologically defined by widespread giant cell transformation. It occurs after the neonatal period, most commonly in the first year of life and uniquely affects pediatric patients. It is still poorly understood and likely underdiagnosed, although in recent years there have been advances in the understanding of its pathogenesis and the liver injury is now hypothesized to be secondary to a humoral immune mechanism. Although no laboratory test specific for the diagnosis currently exists, given its severity, it is fundamental to rule out GCH-AHA when evaluating a patient in the first year of life presenting with AHA and/or with acute liver disease of unknown etiology. While GCH-AHA is progressive in nature as other autoimmune liver disorders, it differs significantly from juvenile autoimmune hepatitis (JAIH) in that a cure can be achieved after several years of intensive treatment in a portion of patients. Conventional first line therapy consist of prednisone/prednisolone combined with azathioprine, however, several immunosuppressive drugs, commonly used in the treatment of JAIH have been tried as second line therapy, including cyclosporine, cyclophosphamide, mycophenolate mofetil, 6-mercaptopurine, calcineurin inhibitors, and sirolimus. Intravenous immunoglobulins have also been used in cases of severe liver dysfunction and/or severe anemia allowing for transitory remission. More recently treatment with B-cell depletion has been attempted in some patients and encouraging results have been reported in refractory cases. Although what constitutes optimal treatment has yet to be determined, the recent progress in the understanding of the pathogenetic mechanisms of GCH-AHA have made positive strides, cautiously pointing toward a hopeful prognosis for some of these patients.

巨细胞肝炎与自身免疫性溶血性贫血相关:最新进展
巨细胞肝炎合并自身免疫性溶血性贫血(GCH-AHA)是一种罕见且严重的疾病,以自身免疫性溶血伴急性肝损伤为特征,组织学上以广泛的巨细胞转化为特征。它发生在新生儿期之后,最常见于生命的第一年,并且仅影响儿科患者。尽管近年来对其发病机制的了解有所进展,肝损伤现在被假设是继发于体液免疫机制,但人们对其仍知之甚少,可能未得到充分诊断。虽然目前没有专门用于诊断的实验室检查,但鉴于其严重程度,在评估患有AHA和/或病因不明的急性肝脏疾病的第一年患者时,排除GCH-AHA是至关重要的。虽然GCH-AHA在本质上与其他自身免疫性肝脏疾病一样是进行性的,但它与少年型自身免疫性肝炎(JAIH)的显著不同之处在于,部分患者在经过数年的强化治疗后可以治愈。传统的一线治疗包括强的松/泼尼松龙联合硫唑嘌呤,然而,一些常用的用于治疗JAIH的免疫抑制药物已被尝试作为二线治疗,包括环孢素、环磷酰胺、霉酚酸酯、6-巯基嘌呤、钙调磷酸酶抑制剂和西罗莫司。静脉注射免疫球蛋白也用于严重肝功能障碍和/或严重贫血的病例,允许短暂缓解。最近在一些患者中尝试了b细胞清除治疗,在难治性病例中报道了令人鼓舞的结果。尽管何为最佳治疗尚未确定,但最近对GCH-AHA发病机制的了解取得了积极进展,谨慎地指出其中一些患者的预后有希望。
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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来源期刊
CiteScore
8.20
自引率
0.00%
发文量
1
期刊介绍: Translational Gastroenterology and Hepatology (Transl Gastroenterol Hepatol; TGH; Online ISSN 2415-1289) is an open-access, peer-reviewed online journal that focuses on cutting-edge findings in the field of translational research in gastroenterology and hepatology and provides current and practical information on diagnosis, prevention and clinical investigations of gastrointestinal, pancreas, gallbladder and hepatic diseases. Specific areas of interest include, but not limited to, multimodality therapy, biomarkers, imaging, biology, pathology, and technical advances related to gastrointestinal and hepatic diseases. Contributions pertinent to gastroenterology and hepatology are also included from related fields such as nutrition, surgery, public health, human genetics, basic sciences, education, sociology, and nursing.
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