• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1016/j.dld.2012.01.003
PMID:22333476
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。

相似文献

1
Liver involvement in children with Familial Mediterranean fever.家族性地中海热患儿的肝脏受累。
Dig Liver Dis. 2012 Aug;44(8):689-93. doi: 10.1016/j.dld.2012.01.003. Epub 2012 Feb 12.
2
A rare cause of ascites: Familial Mediterranean fever.腹水的罕见病因:家族性地中海热。
Turk J Gastroenterol. 2008 Mar;19(1):64-8.
3
[Familial Mediterranean Fever (FMF): from diagnosis to treatment].[家族性地中海热(FMF):从诊断到治疗]
Sante. 2004 Oct-Dec;14(4):261-6.
4
The efficacy of anakinra in an adolescent with colchicine-resistant familial Mediterranean fever.阿那白滞素治疗一名对秋水仙碱耐药的青少年家族性地中海热的疗效。
Eur J Pediatr. 2008 Jun;167(6):695-6. doi: 10.1007/s00431-007-0547-3. Epub 2007 Jun 23.
5
Familial Mediterranean fever--a not so unusual cause of abdominal pain.家族性地中海热——腹痛的一个并非不常见的病因。
Best Pract Res Clin Gastroenterol. 2005 Apr;19(2):199-213. doi: 10.1016/j.bpg.2004.11.009.
6
Unresponsiveness to colchicine therapy in patients with familial Mediterranean fever homozygous for the M694V mutation.对家族性地中海热 M694V 突变纯合子患者的秋水仙碱治疗无反应。
J Rheumatol. 2010 Jan;37(1):182-9. doi: 10.3899/jrheum.090273. Epub 2009 Dec 15.
7
Boundaries between familial Mediterranean fever and juvenile spondyloarthritis: Analysis of three French retrospective cohorts.家族性地中海热与青少年脊柱关节炎的鉴别:法国三个回顾性队列研究分析。
Joint Bone Spine. 2018 Dec;85(6):733-739. doi: 10.1016/j.jbspin.2018.01.010. Epub 2018 Feb 13.
8
Colchicine-responsive chronic recurrent multifocal osteomyelitis with MEFV mutations: a variant of familial Mediterranean fever?伴有MEFV突变的对秋水仙碱敏感的慢性复发性多灶性骨髓炎:家族性地中海热的一种变异型?
Rheumatology (Oxford). 2010 Nov;49(11):2221-3. doi: 10.1093/rheumatology/keq157. Epub 2010 Jun 4.
9
[A three-year-old girl with abdominal pain and fever].[一名患有腹痛和发热的三岁女童]
Tidsskr Nor Laegeforen. 2010 Mar 11;130(5):494-5. doi: 10.4045/tidsskr.09.0692.
10
Bronchoalveolar carcinoma in a patient with recurrent familial Mediterranean attacks, fibrothorax, and treatment with colchicine.一名患有复发性家族性地中海热发作、纤维胸并接受秋水仙碱治疗的患者发生支气管肺泡癌。
Isr Med Assoc J. 1999 Oct;1(2):121-2.

引用本文的文献

1
Characteristics and course of patients with AA amyloidosis: single centre experience with 174 patients from Turkey.土耳其单中心 174 例患者的 AA 淀粉样变性特征和病程:单中心经验。
Rheumatology (Oxford). 2024 Feb 1;63(2):319-328. doi: 10.1093/rheumatology/kead465.
2
Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases.成人发病单基因自身炎症性疾病的遗传与临床鉴别要点。
Mediators Inflamm. 2019 Dec 31;2019:3293145. doi: 10.1155/2019/3293145. eCollection 2019.
3
Familial Mediterranean Fever: an unusual cause of liver disease.
家族性地中海热:一种不常见的肝病病因。
Ital J Pediatr. 2019 Sep 18;45(1):121. doi: 10.1186/s13052-019-0712-0.
4
An adult case of atypical familial Mediterranean fever (pyrin-associated autoinflammatory disease) similar to adult-onset Still's disease.一例类似于成人斯蒂尔病的非典型家族性地中海热(与吡啉相关的自身炎症性疾病)成人病例。
Clin Case Rep. 2019 Mar 12;7(4):801-805. doi: 10.1002/ccr3.2102. eCollection 2019 Apr.
5
Severe liver involvement in two patients with long-term history of fever: remember familial Mediterranean fever.两名长期发热患者出现严重肝脏受累:警惕家族性地中海热。
BMJ Case Rep. 2016 Sep 22;2016:bcr2016216941. doi: 10.1136/bcr-2016-216941.
6
Autoinflammatory diseases: a possible cause of thrombosis?自身炎症性疾病:血栓形成的一个可能原因?
Thromb J. 2015 May 12;13:19. doi: 10.1186/s12959-015-0049-x. eCollection 2015.
7
Non-canonical manifestations of familial Mediterranean fever: a changing paradigm.家族性地中海热的非典型表现:不断变化的模式
Clin Rheumatol. 2015 Sep;34(9):1503-11. doi: 10.1007/s10067-015-2916-z. Epub 2015 Mar 13.