Anti-NMDA receptor encephalitis: report of ten cases and comparison with viral encephalitis

被引:201
作者
Gable, M. S. [1 ,2 ]
Gavali, S. [3 ]
Radner, A. [4 ]
Tilley, D. H. [5 ]
Lee, B. [6 ]
Dyner, L. [7 ]
Collins, A. [8 ]
Dengel, A. [9 ]
Dalmau, J. [10 ]
Glaser, C. A. [1 ,3 ]
机构
[1] Calif Dept Hlth Serv, Viral & Rickettsial Dis Lab, Richmond, CA 94804 USA
[2] Univ Calif San Francisco, Dept Psychiat, Fresno, CA USA
[3] Calif Dept Publ Hlth, Viral & Rickettsial Dis Lab, Div Communicable Dis Control, Ctr Infect Dis, Richmond, CA USA
[4] Salinas Valley Mem Hosp, Salinas, CA USA
[5] USN, Div Infect Dis, San Diego Med Ctr, San Diego, CA 92152 USA
[6] Childrens Hosp & Res Ctr Oakland, Div Infect Dis, Oakland, CA USA
[7] Lucile Packard Childrens Hosp, Palo Alto, CA USA
[8] Univ Colorado, Dept Pediat, Sect Child Neurol, Denver, CO 80202 USA
[9] Loma Linda Univ, Med Ctr, Loma Linda, CA USA
[10] Univ Penn, Dept Neurol, Div Neurooncol, Philadelphia, PA 19104 USA
关键词
PARANEOPLASTIC LIMBIC ENCEPHALITIS; POTASSIUM CHANNEL ANTIBODY; IMMATURE OVARIAN TERATOMA; NERVOUS-SYSTEM; DIAGNOSIS; SCHIZOPHRENIA; HYPOFUNCTION; INFECTIONS; PATHOPHYSIOLOGY; SYMPTOMS;
D O I
10.1007/s10096-009-0799-0
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The California Encephalitis Project (CEP), established in 1998 to explore encephalitic etiologies, has identified patients with N-methyl-D-aspartate receptor (NMDAR) antibodies, the likely etiology of their encephalitis. This study compares the presentation of such patients to those with viral encephalitis, so that infectious disease clinicians may identify individuals with this treatable disorder. Patients were physician-referred, and standardized forms were used to gather demographic, clinical, and laboratory data. Features of anti-NMDAR+ patients were compared with the viral encephalitides of enteroviral (EV), rabies, and herpes simplex-1 (HSV-1) origins. Sixteen cases with confirmed viral etiologies were all negative on NMDAR antibody testing. Ten anti-NMDAR+ patients were profiled with a median age of 18.5 years (range 11-31 years). None were Caucasian. They had a characteristic progression with prominent psychiatric symptoms, autonomic instability, significant neurologic abnormalities, and seizures. Two had a teratoma, and, of the remaining eight, four had serologic evidence of acute Mycoplasma infection. The clinical and imaging features of anti-NMDAR+ patients served to differentiate this autoimmune disorder from HSV-1, EV, and rabies. Unlike classic paraneoplastic encephalitis, anti-NMDAR encephalitis affects younger patients and is often treatable. The association of NMDAR antibodies in patients with possible Mycoplasma pneumoniae infection warrants further study.
引用
收藏
页码:1421 / 1429
页数:9
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