Polyneuropathy and noncompressive cauda equina syndrome as manifestation of systemic lupus erythematosus: a case report.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Ahmad Tirmizi Jobli, Sharifah Aishah Wan, Cheng Lay Teh, Yaw Kiet Cheong, Cindy Hui San Kueh
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引用次数: 0

Abstract

Background: Neuropsychiatric systemic lupus erythematosus covers a wide range of central nervous system and peripheral nervous system conditions. We report a rare case of a man with progressive muscle weakness and cauda equina syndrome.

Case presentation: A 32-year-old man of Chinese ethnicity presented with a 2-month history of progressive muscle weakness of the upper and lower limbs, associated with inflammatory joint pains, and rashes over the upper and lower limbs. Examination showed post-inflammatory hyperpigmentation over the upper and lower limbs and weakness in the proximal muscles of the upper and lower limbs. Laboratory investigations showed anemia, leukopenia, lymphopenia, positive antinuclear antibodies, positive anti-double-stranded deoxyribonucleic acid antibodies, positive anti-Smith antibodies, and positive anti-ribosomal P protein antibodies. He later developed acute urinary incontinence and weak anal tone. Magnetic resonance imaging of the spine showed leptomeningeal enhancement of the cauda equina. He was diagnosed with neuropsychiatric lupus with peripheral polyneuropathy and cauda equina syndrome. His condition was complicated with an infection and pulmonary embolism, but he eventually recovered with treatment. He was treated with high-dose steroids, hydroxychloroquine, intravenous immunoglobulin, anticoagulation, cyclophosphamide, and subsequently, mycophenolate mofetil.

Conclusion: This case highlights the rarity of peripheral neuropathy and noncompressive cauda equina syndrome in systemic lupus erythematosus. A collaborative effort by clinicians in multiple fields is required to achieve a diagnosis and satisfactory treatment in this patient.

系统性红斑狼疮表现为多神经病变和非压迫性马尾综合征1例。
背景:神经精神系统性红斑狼疮涵盖了广泛的中枢神经系统和周围神经系统疾病。我们报告一个罕见的情况下,男子进行性肌肉无力和马尾综合征。病例介绍:32岁男性,华裔,上肢和下肢进行性肌无力2个月,伴有炎症性关节痛,上肢和下肢出现皮疹。检查显示上肢和下肢炎症后色素沉着,上肢和下肢近端肌肉无力。实验室检查显示贫血、白细胞减少、淋巴细胞减少、抗核抗体阳性、抗双链脱氧核糖核酸抗体阳性、抗史密斯抗体阳性、抗核糖体P蛋白抗体阳性。他后来出现急性尿失禁和肛门张力弱。脊柱的核磁共振成像显示马尾脑膜轻脑膜增强。他被诊断为神经精神性狼疮伴周围多神经病变和马尾综合征。他的病情因感染和肺栓塞而变得复杂,但他最终通过治疗恢复了健康。他接受了大剂量类固醇、羟氯喹、静脉注射免疫球蛋白、抗凝剂、环磷酰胺和随后的霉酚酸酯治疗。结论:本病例强调了周围神经病变和非压迫性马尾综合征在系统性红斑狼疮中的罕见性。需要临床医生在多个领域的合作努力才能对该患者进行诊断和满意的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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