Fogel Brent, Cardenas Doris, Ovbiagele Bruce
Department of Neurology, UCLA Medical Center, Los Angeles, California 90095, USA.
Neurologist. 2006 Sep;12(5):271-3. doi: 10.1097/01.nrl.0000237119.00864.d7.
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disorder which can present with a variety of neurologic and psychiatric complications. Currently, there are no consensus neuroimaging findings associated with neuropsychiatric SLE.
We describe the unusual neuroimaging findings in a patient with SLE and a history of epilepsy who presented to a tertiary care emergency department with features of neuropsychiatric lupus, as well as recent seizures. Magnetic resonance imaging of the brain revealed an isolated lesion with T2 signal hyperintensity and restricted diffusion in the midline splenium of the corpus callosum.
While establishing the precise etiology underlying the clinical and radiographic observations in this case is difficult, several possibilities are discussed, including acute ischemia and epileptic sequelae. The location of the patient's lesion in a region potentially associated with pure psychotic disorders raises the possibility that such a lesion may be sufficient to produce acute behavior changes and psychotic features in certain patients.
系统性红斑狼疮(SLE)是一种多系统自身免疫性疾病,可出现多种神经和精神并发症。目前,尚无与神经精神性SLE相关的共识性神经影像学表现。
我们描述了一名患有SLE且有癫痫病史的患者的异常神经影像学表现,该患者因神经精神性狼疮特征以及近期发作而就诊于三级医疗急诊科。脑部磁共振成像显示胼胝体压部中线处有一个孤立病变,T2信号高且弥散受限。
虽然很难确定该病例临床和影像学表现的确切病因,但讨论了几种可能性,包括急性缺血和癫痫后遗症。患者病变位于可能与单纯精神障碍相关的区域,这增加了这种病变可能足以在某些患者中产生急性行为改变和精神症状的可能性。