Caprai Silvia, Vajro Pietro, Ventura Alessandro, Sciveres Marco, Maggiore Giuseppe
Department of Reproductive and Developmental Medicine, University of Pisa, Pisa, Italy.
Clin Gastroenterol Hepatol. 2008 Jul;6(7):803-6. doi: 10.1016/j.cgh.2007.12.002. Epub 2008 Feb 7.
BACKGROUND & AIMS: Celiac patients are at risk to develop an autoimmune liver disease. The aim of this study was to describe the clinical features of children and adolescents presenting with an autoimmune liver disease associated with celiac disease.
A retrospective multicenter national survey was made for the period 1990-2005.
Among 140 pediatric patients with autoimmune liver disease in italy, we identified 23 with celiac disease: 19 with autoimmune hepatitis, 2 with autoimmune cholangitis, and 2 with overlap syndrome. Diagnosis of celiac disease preceded the diagnosis of liver disease in 18 of them, but elevation of aminotransferase activity was present in 16 when celiac disease was diagnosed. Acute hepatitis developed in 2 infants on gluten-free diet, and a hidden celiac disease was discovered in 5 other patients. Nineteen patients had liver-related non-organ-specific autoantibodies. Liver histology showed inflammatory lesions with features of autoimmune damage and different degrees of fibrosis in all of them and cirrhosis in 4. All patients, on gluten-free diet, achieved remission on immunosuppressive therapy, 14 relapsed because of discontinuation of therapy or during spontaneous gluten challenge, 20 are still on immunosuppressive treatment, and 3 could stop therapy.
Autoimmune liver diseases are frequently associated with celiac disease, but they might remain undiagnosed because of lack of symptoms, because of absence of liver-specific autoantibodies, or because of a misdiagnosis of celiac hepatitis. Acute hepatitis in celiac patients should induce one to suspect an autoimmune origin. Patients with autoimmune liver disease might have a hidden celiac disease, suggesting a rigorous check in any cryptogenic liver disease.
乳糜泻患者有患自身免疫性肝病的风险。本研究旨在描述患有与乳糜泻相关的自身免疫性肝病的儿童和青少年的临床特征。
对1990年至2005年期间进行了一项回顾性多中心全国性调查。
在意大利的140例患有自身免疫性肝病的儿科患者中,我们确定了23例患有乳糜泻:19例患有自身免疫性肝炎,2例患有自身免疫性胆管炎,2例患有重叠综合征。其中18例乳糜泻的诊断先于肝病的诊断,但在诊断乳糜泻时,16例存在转氨酶活性升高。2例婴儿在无麸质饮食时发生急性肝炎,另外5例患者发现隐匿性乳糜泻。19例患者有肝脏相关的非器官特异性自身抗体。肝脏组织学显示所有患者均有具有自身免疫损伤特征和不同程度纤维化的炎性病变,4例有肝硬化。所有患者采用无麸质饮食,在免疫抑制治疗后病情缓解,14例因治疗中断或在自发麸质激发试验期间复发,20例仍在接受免疫抑制治疗,3例可以停止治疗。
自身免疫性肝病常与乳糜泻相关,但由于缺乏症状、缺乏肝脏特异性自身抗体或乳糜泻性肝炎误诊等原因,可能仍未被诊断。乳糜泻患者的急性肝炎应促使人们怀疑其自身免疫性起源。自身免疫性肝病患者可能有隐匿性乳糜泻,提示对任何原因不明的肝病进行严格检查。