Jagtap Sujit Abajirao, Das Gopal Krishna, Kambale Harsha J, Radhakrishnan Ashalatha, Nair M D
Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.
Department of Imaging Sciences and Intervention Radiology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.
Ann Indian Acad Neurol. 2014 Apr;17(2):161-5. doi: 10.4103/0972-2327.132615.
Limbic encephalitis (LE) is characterized by rapidly progressive short-term memory loss, psychiatric symptoms and seizures. We describe the clinical spectrum, underlying etiology and long-term follow-up of patients with LE from India.
This prospective study included patients during the period of January 2009 and December 2011 with the clinical features consistent with LE with one or more of the following: (1) Magnetic resonance imaging (MRI) evidence of temporal lobe involvement; (2) cerebrospinal fluid inflammatory abnormalities, or (3) detection of antineuronal antibodies. Patients with metastasis, infection, metabolic and nutritional deficits, stroke, were excluded.
There were 16 patients (9 females), mean age of presentation was 36.6 years (range 15-69 years). The mean duration of symptoms before presentation was 11 months (range 5 days-2 years). The most common symptom at presentation was short-term memory impairment in 7 patients followed by seizures in 5 and behavioral changes in three. Nine patients had seizures, 11 had change in behavior, language involvement in eight, cerebellar features in 3 and autonomic dysfunction in two. Four patients had associated malignancy, 3 of four presented with neurological symptoms and on investigations found to be have malignancy. Antineuronal antibody testing was done in 6 of 12 non paraneoplastic and two paraneoplastic patients, one positive for N-methyl-D-aspartate and one for anti-Hu antibody. MRI brain showed typical fluid attenuated inversion recovery or T2 bilateral temporal lobe hyperintensities in 50% of patients. At a mean follow-up of 21 months (3-36 months), 10 patients improved, 4 patients remained same and two patients expired.
Early recognition of LE is important based upon clinical, MRI data in the absence of antineuronal surface antibody screen in developing nations. Early institution of immunotherapy will help in improvement in outcome of these patients in long-term.
边缘叶脑炎(LE)的特征为快速进展的短期记忆丧失、精神症状和癫痫发作。我们描述了来自印度的LE患者的临床谱、潜在病因及长期随访情况。
这项前瞻性研究纳入了2009年1月至2011年12月期间具有与LE相符临床特征的患者,这些特征包括以下一项或多项:(1)磁共振成像(MRI)显示颞叶受累的证据;(2)脑脊液炎症异常,或(3)抗神经元抗体检测阳性。排除有转移、感染、代谢和营养缺乏、中风的患者。
共16例患者(9例女性),平均就诊年龄为36.6岁(范围15 - 69岁)。就诊前症状的平均持续时间为11个月(范围5天至2年)。就诊时最常见的症状是7例患者出现短期记忆障碍,其次是5例癫痫发作和3例行为改变。9例患者有癫痫发作,11例有行为改变,8例有语言受累,3例有小脑特征,2例有自主神经功能障碍。4例患者伴有恶性肿瘤,其中3例在出现神经症状并经检查发现患有恶性肿瘤。12例非副肿瘤性患者和2例副肿瘤性患者中的6例进行了抗神经元抗体检测,1例N - 甲基 - D - 天冬氨酸抗体阳性,1例抗Hu抗体阳性。脑部MRI显示50%的患者有典型的液体衰减反转恢复序列或T2加权像双侧颞叶高信号。平均随访21个月(3 - 36个月)时,10例患者病情改善,4例患者病情无变化,2例患者死亡。
在发展中国家,基于临床和MRI数据,在未进行抗神经元表面抗体筛查的情况下,早期识别LE很重要。早期给予免疫治疗将有助于长期改善这些患者的预后。