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1
Anti-glutamic Acid decarboxylase antibody-associated ataxia as an extrahepatic autoimmune manifestation of hepatitis C infection: a case report.抗谷氨酸脱羧酶抗体相关性共济失调作为丙型肝炎感染的一种肝外自身免疫表现:一例报告
Case Rep Neurol Med. 2011;2011:975152. doi: 10.1155/2011/975152. Epub 2011 Jul 10.
2
Immune Mediated Cerebellar Ataxia: An Unknown Manifestation of Graft-versus-Host Disease.免疫介导小脑共济失调:移植物抗宿主病的一种未知表现。
Acta Haematol. 2019;141(1):19-22. doi: 10.1159/000494423. Epub 2018 Nov 15.
3
High Titer of Circulating Antiglutamic Acid Decarboxylase Antibodies in a Patient with Cerebellar Ataxia and Type 1 Diabetes.一名患有小脑共济失调和1型糖尿病的患者体内存在高滴度循环谷氨酸脱羧酶抗体
Conn Med. 2017 Mar;81(3):161-164.
4
Low-Titre GAD Antibody-Associated Late-Onset Cerebellar Ataxia with a Significant Clinical Response to Intravenous Immunoglobulin Treatment.低滴度谷氨酸脱羧酶抗体相关迟发性小脑共济失调对静脉注射免疫球蛋白治疗有显著临床反应
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Cerebellar disease associated with anti-glutamic acid decarboxylase antibodies: review.与抗谷氨酸脱羧酶抗体相关的小脑疾病:综述。
J Neural Transm (Vienna). 2017 Oct;124(10):1171-1182. doi: 10.1007/s00702-017-1754-3. Epub 2017 Jul 8.
6
A Case of Treatment Resistance and Complications in a Patient with Stiff Person Syndrome and Cerebellar Ataxia.1例僵人综合征合并小脑共济失调患者的治疗抵抗及并发症
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7
Autoantibodies to glutamic acid decarboxylase in three patients with cerebellar ataxia, late-onset insulin-dependent diabetes mellitus, and polyendocrine autoimmunity.三名患有小脑共济失调、迟发性胰岛素依赖型糖尿病和多内分泌自身免疫的患者体内谷氨酸脱羧酶自身抗体。
Neurology. 1997 Oct;49(4):1026-30. doi: 10.1212/wnl.49.4.1026.
8
[A case of human immunodeficiency virus infection with cerebellar ataxia that suggested by an association with autoimmunity].[一例与自身免疫相关提示为小脑性共济失调的人类免疫缺陷病毒感染病例]
Rinsho Shinkeigaku. 2016 Apr 28;56(4):255-9. doi: 10.5692/clinicalneurol.cn-000851. Epub 2016 Mar 24.
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Spontaneous downbeat nystagmus as a clue for the diagnosis of ataxia associated with anti-GAD antibodies.自发性下跳性眼球震颤作为诊断抗谷氨酸脱羧酶抗体相关共济失调的线索。
J Neurol Sci. 2015 Dec 15;359(1-2):21-3. doi: 10.1016/j.jns.2015.10.024. Epub 2015 Oct 20.
10
Intravenous immunoglobulin and rituximab for cerebellar ataxia with glutamic acid decarboxylase autoantibodies.静脉注射免疫球蛋白和利妥昔单抗治疗谷氨酸脱羧酶自身抗体相关小脑性共济失调。
Cerebellum. 2014 Jun;13(3):318-22. doi: 10.1007/s12311-013-0534-3.

引用本文的文献

1
Anti-glutamic acid decarboxylase antibody (GAD) syndromes may have more aggressive disease course in African Americans and early onset of presentation compare to Caucasians group.与白种人群体相比,抗谷氨酸脱羧酶抗体(GAD)综合征在非裔美国人中可能具有更具侵袭性的病程且发病更早。
eNeurologicalSci. 2019 Sep 11;17:100208. doi: 10.1016/j.ensci.2019.100208. eCollection 2019 Dec.
2
Clinical Spectrum of Stiff Person Syndrome: A Review of Recent Reports.僵人综合征的临床谱:近期报告综述
Tremor Other Hyperkinet Mov (N Y). 2016 Mar 4;6:340. doi: 10.7916/D85M65GD. eCollection 2016.
3
Intravenous immunoglobulin and rituximab for cerebellar ataxia with glutamic acid decarboxylase autoantibodies.静脉注射免疫球蛋白和利妥昔单抗治疗谷氨酸脱羧酶自身抗体相关小脑性共济失调。
Cerebellum. 2014 Jun;13(3):318-22. doi: 10.1007/s12311-013-0534-3.

本文引用的文献

1
Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).丙型肝炎病毒感染患者的系统性自身免疫性疾病:1020例病例的特征(HISPAMEC注册研究)
J Rheumatol. 2009 Jul;36(7):1442-8. doi: 10.3899/jrheum.080874. Epub 2009 Apr 15.
2
Anemia after bariatric surgery: more than just iron deficiency.减肥手术后的贫血:不仅仅是缺铁。
Nutr Clin Pract. 2009 Apr-May;24(2):217-26. doi: 10.1177/0884533609332174.
3
Autoimmune thrombocytopenia related to chronic hepatitis C virus infection.与慢性丙型肝炎病毒感染相关的自身免疫性血小板减少症
Hematology. 2009 Feb;14(1):49-58. doi: 10.1179/102453309X385106.
4
Prognosis and therapy of Wernicke's encephalopathy after obesity surgery.肥胖症手术后韦尼克脑病的预后与治疗
Am J Gastroenterol. 2008 Dec;103(12):3219. doi: 10.1111/j.1572-0241.2008.02161_19.x.
5
Endocrine manifestations of hepatitis C virus infection.丙型肝炎病毒感染的内分泌表现。
Nat Clin Pract Endocrinol Metab. 2009 Jan;5(1):26-34. doi: 10.1038/ncpendmet1027.
6
Stiff-person syndrome with amphiphysin antibodies: distinctive features of a rare disease.伴有抗 amphiphysin 抗体的僵人综合征:一种罕见疾病的独特特征
Neurology. 2008 Dec 9;71(24):1955-8. doi: 10.1212/01.wnl.0000327342.58936.e0. Epub 2008 Oct 29.
7
Characteristics of fulminant type 1 diabetes mellitus.暴发性1型糖尿病的特征。
Med Sci Monit. 2008 Oct;14(10):CS97-101.
8
Mixed cryoglobulinemia.混合性冷球蛋白血症
Orphanet J Rare Dis. 2008 Sep 16;3:25. doi: 10.1186/1750-1172-3-25.
9
Gluten ataxia.麸质共济失调
Cerebellum. 2008;7(3):494-8. doi: 10.1007/s12311-008-0052-x.
10
Spectrum of neurological syndromes associated with glutamic acid decarboxylase antibodies: diagnostic clues for this association.与谷氨酸脱羧酶抗体相关的神经综合征谱系:这种关联的诊断线索
Brain. 2008 Oct;131(Pt 10):2553-63. doi: 10.1093/brain/awn183. Epub 2008 Aug 7.

抗谷氨酸脱羧酶抗体相关性共济失调作为丙型肝炎感染的一种肝外自身免疫表现:一例报告

Anti-glutamic Acid decarboxylase antibody-associated ataxia as an extrahepatic autoimmune manifestation of hepatitis C infection: a case report.

作者信息

Awad Amer, Stüve Olaf, Mayo Marlyn, Alkawadri Rafeed, Estephan Bachir

机构信息

Baton Rouge Neurology Associates, Baton Rouge General Medical Center, Baton Rouge, LA, USA.

出版信息

Case Rep Neurol Med. 2011;2011:975152. doi: 10.1155/2011/975152. Epub 2011 Jul 10.

DOI:10.1155/2011/975152
PMID:22937348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3420584/
Abstract

Extrahepatic immunological manifestations of hepatitis C virus (HCV) are well described. In addition, antiglutamic acid decarboxylase (GAD) antibody-associated cerebellar ataxia is well-established entity. However, there have been no reports in the literature of anti-GAD antibody-associated ataxia as an extrahepatic manifestation of HCV infection. We report the case of a young woman with chronic hepatitis C virus and multiple extrahepatic autoimmune diseases including Sjögren syndrome and pernicious anemia who presented with subacute midline cerebellar syndrome and was found to have positive antiglutamic acid decarboxylase (GAD) antibody in the serum and cerebrospinal fluid. An extensive diagnostic workup to rule out neoplastic growths was negative, suggesting the diagnosis of nonparaneoplastic antiglutamic acid decarboxylase antibody-associated cerebellar ataxia as an additional extrahepatic manifestation of hepatitis C virus infection. The patient failed to respond to high-dose steroids and intravenous immunoglobulin. Treatment with the monoclonal antibody rituximab stabilized the disease. We postulate that anti-GAD associated ataxia could be an extrahepatic manifestation of HCV infection.

摘要

丙型肝炎病毒(HCV)的肝外免疫表现已有充分描述。此外,抗谷氨酸脱羧酶(GAD)抗体相关的小脑共济失调是一种公认的疾病。然而,文献中尚无关于抗GAD抗体相关共济失调作为HCV感染肝外表现的报道。我们报告了一例患有慢性丙型肝炎病毒且伴有多种肝外自身免疫性疾病(包括干燥综合征和恶性贫血)的年轻女性病例,该患者出现亚急性中线小脑综合征,血清和脑脊液中抗谷氨酸脱羧酶(GAD)抗体呈阳性。为排除肿瘤生长进行的广泛诊断检查结果为阴性,提示诊断为非副肿瘤性抗谷氨酸脱羧酶抗体相关小脑共济失调,这是丙型肝炎病毒感染的另一种肝外表现。该患者对大剂量类固醇和静脉注射免疫球蛋白治疗无反应。使用单克隆抗体利妥昔单抗治疗使病情稳定。我们推测抗GAD相关共济失调可能是HCV感染的肝外表现。