Systemic Lupus Erythematosus and Third Nerve Palsy: Unusual Presentation and Review of the Literature

被引:0
|
作者
Natarajan, Divya [1 ]
Kannam, Mohan [2 ]
Reddy, M. Vishnu Vardhan [3 ]
Sachdeva, Virender [2 ]
机构
[1] LV Prasad Eye Inst, Dept Pediat Ophthalmol Strabismus & Neuroopthalmo, Child Sight Inst, Miriam Hyman Childrens Eye Care Ctr, Bhubaneswar, India
[2] LV Prasad Eye Inst, Dept Pediat Ophthalmol Strabismus & Neuroopthalmo, Child Sight Inst, Nimmagadda Prasad Childrens Eye Care Ctr, GMR Varalakshmi Campus, Visakhapatnam 530040, Andhra Pradesh, India
[3] Vizag Rheumatol & Immunol Ctr, Visakhapatnam, Andhra Pradesh, India
关键词
Isolated; incomplete third cranial nerve palsy; systemic lupus erythematosus; pyrexia of unknown origin; pancytopaenia; INITIAL MANIFESTATION;
D O I
10.1080/01658107.2021.1912113
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report the case of a young female with pyrexia of unknown origin, cutaneous macules and an incomplete third cranial nerve palsy, that led to the diagnosis of systemic lupus erythematosus (SLE) with neurological manifestations. Her visual acuity was normal. Fundus examination showed cotton wool spots in both eyes. Neuroimaging was also normal. Systemic work up revealed pancytopaenia, hypocomplementaemia, and the presence of multiple autoantibodies including anti-double stranded deoxyribonucleic acid and lupus anticoagulant. She was effectively treated with intravenous pulsed corticosteroid therapy, cyclophosphamide, and oral hydroxychloroquine. This case highlights the uncommon involvement of cranial nerve mononeuropathy in SLE, the importance of systemic examination and autoimmune workup in young patients with such a presentation.
引用
收藏
页码:109 / 114
页数:6
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