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特发性颅内高压作为系统性红斑狼疮的初始表现

Idiopathic intracranial hypertension as an initial presentation of systemic lupus erythematosus.

作者信息

Maloney Keisha

机构信息

University of the West Indies, Kingston, Jamaica.

出版信息

BMJ Case Rep. 2013 Aug 13;2013:bcr2013010223. doi: 10.1136/bcr-2013-010223.

DOI:10.1136/bcr-2013-010223
PMID:23943808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3761693/
Abstract

A 14-year-old girl with no known illness presented with a several week history of headaches and vomiting. The patient also reported having joint pain and swelling to the wrists and knees. She had no prior history of headaches, use of hormonal contraception or other medications, recent weight changes or family history of autoimmune disease. Blood pressure temperature, height and weight were normal. She was alert, there was alopecia, cervical lympadenopathy, symmetrical synovitis to the wrists, bilateral papilloedema and cranial nerve VI palsy. Laboratory investigations revealed a normochromic normocytic anaemia, leucopenia and lymphopenia. Serum chemistries were normal. CT of the brain was normal. Lumbar puncture revealed an opening pressure of greater than 300 mm H2O; cerebrospinal fluid (CSF) analysis was normal. HIV antibodies were non-reactive. Despite treatment with acetazolamide she developed somnolence. Hence MR venography was performed which showed no evidence of cerebral vein thrombosis. Further investigations revealed a positive direct coombs test, positive antinuclear antibodies (ANA) positive antidouble-stranded DNA (dsDNA) and false positive VDRL. Complement levels were reduced. Anti-Smith, anticardiolipin antibodies and lupus anticoagulant were negative.

摘要

一名14岁无已知疾病的女孩出现了数周的头痛和呕吐症状。患者还报告手腕和膝盖有关节疼痛和肿胀。她既往无头痛史、未使用过激素避孕药或其他药物、近期体重无变化,也无自身免疫性疾病家族史。血压、体温、身高和体重均正常。她神志清醒,有脱发、颈部淋巴结病、手腕对称性滑膜炎、双侧视乳头水肿和第六颅神经麻痹。实验室检查显示正细胞正色素性贫血、白细胞减少和淋巴细胞减少。血清化学指标正常。脑部CT正常。腰椎穿刺显示初压大于300 mm H2O;脑脊液(CSF)分析正常。HIV抗体呈阴性。尽管使用乙酰唑胺治疗,她仍出现嗜睡。因此进行了磁共振静脉造影,未显示脑静脉血栓形成的证据。进一步检查显示直接抗人球蛋白试验阳性、抗核抗体(ANA)阳性、抗双链DNA(dsDNA)阳性和VDRL假阳性。补体水平降低。抗史密斯抗体、抗心磷脂抗体和狼疮抗凝物均为阴性。

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本文引用的文献

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Intracranial hypertension with delayed puberty: a rare presentation of juvenile onset systemic lupus erythematosus.颅内压增高伴青春期延迟:幼年发病系统性红斑狼疮的罕见表现。
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Idiopathic intracranial hypertension and systemic lupus erythematosus: a case report and review of the literature.特发性颅内高压与系统性红斑狼疮:一例病例报告及文献综述
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Idiopathic intracranial hypertension (pseudotumor cerebri).特发性颅内高压(假性脑瘤)。
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Increased intracranial pressure related to systemic lupus erythematosus: a 26-year experience.与系统性红斑狼疮相关的颅内压升高:26年的经验
Semin Arthritis Rheum. 2008 Oct;38(2):110-5. doi: 10.1016/j.semarthrit.2007.09.007. Epub 2008 Jan 25.
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Systemic lupus erythematosus presenting with pseudotumor cerebri: a rare association.以假性脑瘤为表现的系统性红斑狼疮:一种罕见的关联。
Turk J Pediatr. 2007 Jan-Mar;49(1):98-101.
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Mortality related to cerebrovascular disease in systemic lupus erythematosus.系统性红斑狼疮中与脑血管疾病相关的死亡率
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Neuropsychiatric events at the time of diagnosis of systemic lupus erythematosus: an international inception cohort study.系统性红斑狼疮诊断时的神经精神事件:一项国际初始队列研究。
Arthritis Rheum. 2007 Jan;56(1):265-73. doi: 10.1002/art.22305.
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Pseudotumor cerebri.假性脑瘤
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