Srikakulam Sundeep, Askanese Anca
New York University Hospital for Joint Diseases, Seligman Center for Advanced Therapeutics, New York, New York 10003, USA.
Bull NYU Hosp Jt Dis. 2012;70(2):115-9.
Neuropsychiatric (NP) systemic lupus erythematosus (SLE) is a complex entity comprising 19 different discrete syndromes. We report a case of a 32-year-old female with SLE and new onset neurological symptoms and radiographic evidence of a contrast enhancing lesion on brain MRI. The lesion was successfully excised and found to be granulomatous in nature. Infection and malignant etiologies were ruled out suggesting that the lesion was due to SLE. Subsequently, the development of multiple reversible hyperintense signal abnormalities on brain MRI suggested the possibility of posterior reversible encephalopathy syndrome (PRES). The lesions resolved after the withdrawal of immunosuppression. This article reviews both the clinical and pathological complexity of PRES in SLE and the state of the current literature. We conclude that more data is required to understand the spectrum of PRES and its management in SLE patients.
神经精神性(NP)系统性红斑狼疮(SLE)是一种复杂的病症,包含19种不同的独立综合征。我们报告一例32岁女性SLE患者,出现新发神经症状,脑部MRI有强化病灶的影像学证据。该病灶成功切除,病理显示为肉芽肿性。排除感染和恶性病因,提示该病灶由SLE所致。随后,脑部MRI出现多个可逆性高信号异常,提示可能为后部可逆性脑病综合征(PRES)。停用免疫抑制剂后病灶消退。本文综述了SLE中PRES的临床和病理复杂性以及当前文献状况。我们得出结论,需要更多数据来了解SLE患者中PRES的范围及其管理。