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家族性地中海热患儿的肝脏受累。

Liver involvement in children with Familial Mediterranean fever.

机构信息

Department of Pediatric Gastroenterology, Hepatology and Nutrition, Dörtçelik Pediatric Hospital, Bursa, Turkey.

出版信息

Dig Liver Dis. 2012 Aug;44(8):689-93. doi: 10.1016/j.dld.2012.01.003. Epub 2012 Feb 12.

Abstract

AIM

Familial Mediterranean fever is characterised by recurrent, febrile, inflammatory attacks of the serosal membranes. Prolonged inflammatory response is triggered secondary to cytokine stimulation due to reduced activity of pyrin. Inflammatory cytokines play major role in the pathogenesis of acute liver injury; and chronic, recurrent cytokine production may cause chronic hepatitis/cirrhosis. We aimed to analyse liver involvement in children with Familial Mediterranean fever.

PATIENTS

The study included 58 patients with Familial Mediterranean fever. Patients with liver involvement were examined in detail.

RESULTS

Liver involvement was seen in 11 of 58 patients (18.9%). Two patients (3.4%) had abnormal liver enzymes during the diagnostic evaluation, whilst 9 patients (15.5%) were admitted with the features of liver diseases, and had final diagnosis of Familial Mediterranean fever (2 had Budd-Chiari syndrome, 5 had chronic hepatitis/cirrhosis, 2 had acute hepatitis). None of the demographic factors or laboratory findings was different between the patients with or without liver involvement M694V allele was more common in patients with liver involvement but did not reach significant difference (50% vs. 33.6%, p=0.21). All the patients showed clinical and laboratory improvement after colchicine.

CONCLUSION

Paediatric hepatologists must keep Familial Mediterranean fever in mind in the patients with cryptogenic hepatitis/cirrhosis especially in regions where hereditary inflammatory diseases are common.

摘要

目的

家族性地中海热的特征是反复发作的发热、炎症性浆膜炎。由于 pyrin 活性降低,细胞因子刺激引发持续性炎症反应。炎症细胞因子在急性肝损伤发病机制中起主要作用;慢性、反复的细胞因子产生可能导致慢性肝炎/肝硬化。我们旨在分析儿童家族性地中海热的肝脏受累情况。

患者

本研究纳入了 58 例家族性地中海热患者。详细检查了有肝脏受累的患者。

结果

58 例患者中 11 例(18.9%)有肝脏受累。2 例(3.4%)在诊断评估时出现肝酶异常,9 例(15.5%)因肝脏疾病特征入院,最终诊断为家族性地中海热(2 例为布加综合征,5 例为慢性肝炎/肝硬化,2 例为急性肝炎)。有或无肝脏受累的患者之间的人口统计学因素或实验室发现无差异 M694V 等位基因在有肝脏受累的患者中更为常见,但无显著差异(50% vs. 33.6%,p=0.21)。所有患者在用秋水仙碱治疗后均表现出临床和实验室改善。

结论

在隐匿性肝炎/肝硬化患者中,儿科肝病学家必须牢记家族性地中海热,特别是在遗传性炎症性疾病常见的地区。

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