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系统性红斑狼疮的神经精神表现:诊断、临床谱及与疾病其他特征的关系。

Neuropsychiatric manifestations of systemic lupus erythematosus: diagnosis, clinical spectrum, and relationship to other features of the disease.

作者信息

Feinglass E J, Arnett F C, Dorsch C A, Zizic T M, Stevens M B

出版信息

Medicine (Baltimore). 1976 Jul;55(4):323-39. doi: 10.1097/00005792-197607000-00004.

DOI:10.1097/00005792-197607000-00004
PMID:781466
Abstract
  1. Among patients with SLE, 71 (51%) had significant neuropsychiatric problems during the course of the disease. In 52 (37%), the nervous system manifestations were secondary to SLE. 2. The most frequent manifestations were psychiatric dysfunction, seizures, long tract signs, cranial neuropathy, and peripheral neuropathy. 3. Psychiatric abnormalities secondary to SLE were characterized by organic features (present in 22 of 24) and by the association of neurologic lesions which were often diffuse or multifocal. 4. An abnormal cerebrospinal fluid was found in 32% of neuropsychiatric episodes in which specimens were obtained. The most frequently abnormal study was the electroencephalogram (71%), and the least frequent was the brain scan (8%). These studies did not correlate with specific clinical patterns. 5. In 63% of the patients, NP manifestations preceded the diagnosis of SLE or occurred within the first year of diagnosed disease, and in most episodes were associated with evidence of clinical and/or serologic activity of the underlying illness. 6. Only two clinical features showed significant and striking correlations with neuropsychiatric involvement, namely vasculitis and thrombocytopenia. The possible pathogenic implications have been discussed. 7. Only 2 of the 140 patients were felt to have steroid-induced psychoses. In approximately one-half of the NP episodes secondary to SLE, patients were receiving no corticosteriods on presentation. Of those developing while patients were on steroids, the majority occurred on low doses or after tapering from higher levels. 8. The immediate prognosis for improvement in neuropsychiatric function was good with 84% of episodes showing complete or partial resolution. Corticosteroids appeared to be of benefit in a substantial number of patients although their precise role is difficult to quantitate. 9. Five and 10 years survivals for the overall population were 94% and 82%, respectively. There were no significant differences in survival for patients with or without nervous system involvement.
摘要
  1. 在系统性红斑狼疮(SLE)患者中,71例(51%)在疾病过程中出现了显著的神经精神问题。52例(37%)的神经系统表现继发于SLE。2. 最常见的表现为精神功能障碍、癫痫发作、长束征、颅神经病变和周围神经病变。3. SLE继发的精神异常以器质性特征为特点(24例中有22例),且常伴有弥漫性或多灶性神经病变。4. 在获取标本的神经精神发作中,32%发现脑脊液异常。最常出现异常的检查是脑电图(71%),最少出现异常的是脑部扫描(8%)。这些检查结果与特定临床模式无相关性。5. 63%的患者神经精神症状出现在SLE诊断之前或确诊疾病的第一年内,且在大多数发作中与潜在疾病的临床和/或血清学活动证据相关。6. 只有两种临床特征与神经精神受累存在显著且明显的相关性,即血管炎和血小板减少症。已对可能的致病影响进行了讨论。7. 140例患者中只有2例被认为患有类固醇诱导的精神病。在SLE继发的神经精神发作中,约一半患者就诊时未接受皮质类固醇治疗。在接受类固醇治疗的患者中出现的发作,大多数发生在低剂量时或从较高剂量减量后。8. 神经精神功能改善的近期预后良好,84%的发作显示完全或部分缓解。皮质类固醇对相当一部分患者似乎有益,尽管其确切作用难以量化。9. 总体人群的5年和10年生存率分别为94%和82%。有无神经系统受累的患者生存率无显著差异。

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