Hepatic damage in gluten sensitive enteropathy.

B Altuntaş, A Kansu, N Girgin
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引用次数: 18

Abstract

Background: Gluten sensitive enteropathy has been reported to occur concomitantly with liver abnormalities, such as primary biliary cirrhosis, chronic active hepatitis and primary sclerosing cholangitis.

Methods: Duodenal biopsy was performed in nine children (all with short stature, five with chronic diarrhea and three with hepatosplenomegaly of unknown etiology) with a possible diagnosis of gluten sensitive enteropathy. All of the patients had different abnormalities in serum aminotransferase levels. With the help of laboratory investigations, viral, autoimmune, metabolic and toxic etiologies which cause hepatic damage were excluded. Liver biopsy was performed in five of these patients, two showing fibrosis and three nonspecific reactive changes. Gliadin antibodies were measured in six cases.

Results: Intestinal mucosal histopathology was compatible with gluten sensitive enteropathy in all patients. While immunoglobulin (Ig) G gliadin antibodies were positive in all cases, only three cases were found to have positive IgA gliadin antibodies. After a gluten-free diet, levels of transaminases fell to normal within 3 months and remained so in seven of these patients. A second intestinal biopsy, which was performed after 1 year of gluten-free diet revealed normal intestinal mucosa in all patients.

Conclusion: Gluten sensitive enteropathy should be considered when evaluating a child with elevated levels of serum transaminase and in cases with cryptogenic liver disease.

麸质敏感性肠病的肝损害。
背景:据报道,麸质敏感性肠病可伴发肝脏异常,如原发性胆汁性肝硬化、慢性活动性肝炎和原发性硬化性胆管炎。方法:对9例可能诊断为麸质敏感性肠病的儿童(均为身材矮小,5例患有慢性腹泻,3例患有病因不明的肝脾肿大)进行十二指肠活检。所有患者血清转氨酶水平均有不同程度的异常。在实验室检查的帮助下,排除了导致肝损害的病毒、自身免疫、代谢和毒性病因。其中5例患者进行了肝活检,2例显示纤维化,3例显示非特异性反应性改变。6例患者检测麦胶蛋白抗体。结果:所有患者的肠黏膜组织病理学均符合麸质敏感性肠病。免疫球蛋白(Ig) G麦胶蛋白抗体在所有病例中均呈阳性,而IgA麦胶蛋白抗体仅在3例中呈阳性。在无麸质饮食后,转氨酶水平在3个月内降至正常水平,并在其中7名患者中保持正常。在无麸质饮食1年后进行的第二次肠道活检显示,所有患者的肠道粘膜正常。结论:在评估血清转氨酶水平升高的儿童和隐源性肝病的病例时,应考虑麸质敏感性肠病。
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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