Veciana M, Becerra J L, Fossas P, Muriana D, Sansa G, Santamarina E, Gaig C, Carreño M, Molins A, Escofet C, Ley M, Vivanco R, Pedro J, Miró J, Falip M
Servei de Neurologia, Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Spain.
Servei de Neurologia, Hospital Germans Trias i Pujol, Badalona, Spain.
Epilepsy Behav. 2015 Aug;49:280-5. doi: 10.1016/j.yebeh.2015.04.032. Epub 2015 Jun 10.
The anti-NMDA receptor (NMDAr) encephalitis-associated syndrome includes neuropsychiatric symptoms, impaired consciousness, seizures, autonomic instability, and hypoventilation. The electroencephalographic (EEG) activity throughout the course of the disease has still not been well documented. We reviewed electroclinical data of patients with NMDAr encephalitis to characterize their EEG and its clinical correlation.
We retrospectively identified 16 patients with NMDAr encephalitis from 8 Spanish medical centers, 15 of whom underwent video-EEG in the acute phase.
In 15 patients (11 females, median age: 37.4, range: 14-87 years), seizures occurred in 9 (60%) and status epilepticus (SE) in 5 (33.3%). Magnetic resonance imaging (MRI) was abnormal in 10 (66.6%), and CSF (cerebrospinal fluid) was normal in 3 and abnormal in 12, with positive PCR (polymerase chain reaction) for Mycoplasma pneumoniae (1/15) and herpes simple virus (1/15). An ovarian teratoma was found in 1 patient and other malignancies (small cell lung carcinoma) in 1 patient. The EEG was abnormal in the acute phase in 14/15 (93.3%). Extreme delta brush (EDB) was observed in 5 (33.3%), and the presence of EDB was associated with SE in all cases. Rhythmic delta activity without EDB was observed in 5 (33.3%), while excessive beta activity was present in 4 (26.6%). Extreme delta brush can follow a pattern of well-characterized electroclinical seizures.
Almost invariably, patients with NMDAr encephalitis had abnormal EEG. The presence of EDB, which can follow a pattern of well-characterized electroclinical seizures, in our patients was associated with seizures and SE. These findings suggest that EDB could be an evolutive pattern of an SE in NMDAr encephalitis. This article is part of a Special Issue entitled "Status Epilepticus".
抗N-甲基-D-天冬氨酸受体(NMDAr)脑炎相关综合征包括神经精神症状、意识障碍、癫痫发作、自主神经功能不稳定和通气不足。该疾病整个病程中的脑电图(EEG)活动仍未得到充分记录。我们回顾了NMDAr脑炎患者的电临床数据,以描述其脑电图特征及其临床相关性。
我们从8家西班牙医疗中心回顾性确定了16例NMDAr脑炎患者,其中15例在急性期接受了视频脑电图检查。
15例患者(11例女性,中位年龄:37.4岁,范围:14 - 87岁),9例(60%)出现癫痫发作,5例(33.3%)出现癫痫持续状态(SE)。10例(66.6%)的磁共振成像(MRI)异常,3例脑脊液(CSF)正常,12例异常,肺炎支原体(1/15)和单纯疱疹病毒(1/15)的聚合酶链反应(PCR)呈阳性。1例患者发现卵巢畸胎瘤,1例患者发现其他恶性肿瘤(小细胞肺癌)。14/15(93.3%)的患者在急性期脑电图异常。5例(33.3%)观察到极慢δ刷(EDB),所有病例中EDB的出现均与SE相关。5例(33.3%)观察到无EDB的节律性δ活动,4例(26.6%)出现过度β活动。极慢δ刷可呈现特征性的电临床癫痫发作模式。
几乎所有NMDAr脑炎患者的脑电图均异常。在我们的患者中,极慢δ刷的出现可呈现特征性的电临床癫痫发作模式,与癫痫发作和癫痫持续状态相关。这些发现表明,极慢δ刷可能是NMDAr脑炎中癫痫持续状态的一种演变模式。本文是名为“癫痫持续状态”的特刊的一部分。