Ohshita Tomohiko, Kawakami Hideshi, Maruyama Hirofumi, Kohriyama Tatsuo, Arimura Kimiyoshi, Matsumoto Masayasu
Department of Clinical Neuroscience and Therapeutics, Hiroshima University, Graduate School of Biomedical Sciences, Hiroshima, Kagoshima, Japan.
J Neurol Sci. 2006 Dec 1;250(1-2):167-9. doi: 10.1016/j.jns.2006.08.003. Epub 2006 Oct 9.
Recently, limbic encephalitis (LE) associated with Voltage-gated potassium channel antibody (VGKC-Ab) has been postulated as a new autoimmune disorder. Most previously reported cases of VGKC-Ab-associated LE were non-paraneoplastic, and reports of a paraneoplastic type are rare. Here we describe a 59-year-old woman with paraneoplastic VGKC-Ab-associated LE preceding the recurrence of invasive thymoma. There was a close temporal relationship between the clinical course and the changes of the VGKC-Ab titer. Unlike many of the non-paraneoplastic VGKC-Ab-associated LE cases, our cases showed the more extensive high intensity lesions on MRI and the absence of seizure and hyponatremia.
最近,与电压门控钾通道抗体(VGKC-Ab)相关的边缘叶脑炎(LE)被认为是一种新的自身免疫性疾病。之前报道的大多数VGKC-Ab相关LE病例为非肿瘤性,而肿瘤性类型的报道很少。在此,我们描述一名59岁女性,在侵袭性胸腺瘤复发之前出现肿瘤性VGKC-Ab相关LE。临床病程与VGKC-Ab滴度变化之间存在密切的时间关系。与许多非肿瘤性VGKC-Ab相关LE病例不同,我们的病例在MRI上显示出更广泛的高强度病变,且无癫痫发作和低钠血症。