Metabotropic Glutamate Receptor Type 1 Autoantibody-Associated Cerebellitis A Primary Autoimmune Disease?

被引:88
作者
Marignier, Romain [1 ,2 ,3 ,4 ]
Chenevier, Florian [1 ,2 ,3 ]
Rogemond, Veronique [4 ]
Smitt, Peter Sillevis [5 ]
Renoux, Christel [1 ,2 ,3 ]
Cavillon, Gaelle [4 ]
Androdias, Geraldine [1 ,2 ,3 ,4 ]
Vukusic, Sandra [1 ,2 ,3 ,4 ]
Graus, Francesc [6 ,7 ]
Honnorat, Jerome [3 ,4 ]
Confavreux, Christian [1 ,2 ,3 ,4 ]
机构
[1] Hosp Civils Lyon, Hop Neurol Pierre Wertheimer, Serv Neurol A, F-69677 Lyon, France
[2] Hosp Civils Lyon, Hop Neurol Pierre Wertheimer, European Database Multiple Sclerosis Coordinating, F-69677 Lyon, France
[3] Unite Mixte Recherche S842, Lyon, France
[4] Inst Natl Sante & Rech Med, U842, Lyon, France
[5] Erasmus MC, Dept Neurol, Rotterdam, Netherlands
[6] Hosp Clin Barcelona, Serv Neurol, Barcelona, Spain
[7] Inst Invest Biomed August Pi & Sunyer, Barcelona, Spain
关键词
LONG-TERM DEPRESSION; DEGENERATION; MGLUR1; CELLS;
D O I
10.1001/archneurol.2010.51
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Objectives: To report the third case of subacute cerebellar ataxia associated with metabotropic glutamate receptor type 1 autoantibodies (mGluR1-Abs), an uncommon syndrome known to be part of the group of paraneoplastic cerebellar degeneration syndromes linked to antineuronal antibodies and previously reported in only 2 other patients with long-term remission of Hodgkin lymphoma, and to discuss the underlying immunopathogenesis. Design: Case report. Setting: University hospital. Patient: A 50-year-old woman admitted for acute severe isolated static and kinetic cerebellar syndrome. Magnetic resonance imaging of the brain showed diffuse abnormal hyperintensity in the whole cerebellum on fluid-attenuated inversion recovery and diffusion sequences. Results: Results of the biological workup were negative for general inflammation, vitamin deficiency, and bacterial and viral infections. Immunohistochemical analysis of the serum and cerebrospinal fluid of the patient demonstrated staining for Purkinje cell bodies and the molecular layer of the cerebellum. Finally, mGluR1-Abs were detected in serum and cerebrospinal fluid by a cell-based assay. Complete clinical examination, thoracoabdominal-pelvic computed tomography, and wholebody fludeoxyglucose F 18-positron emission tomography failed to show any underlying tumor, including Hodgkin lymphoma. The disease was stabilized after a course of intravenous immunoglobulins and continuous mycophenolate mofetil treatment during a follow-up of 40 months. Conclusions: Cerebellitis associated with mGluR1-Abs should be considered in the differential diagnosis of patients with subacute cerebellar ataxia. This first case without any tumor found suggests a possible idiopathic autoimmune rather than a paraneoplastic mechanism. In consideration of this possible primitive autoimmune ataxia involving the directly pathogenic mGluR1-Abs, immunoactive therapy should be initiated as early as possible.
引用
收藏
页码:627 / 630
页数:4
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