2013
DOI: 10.1136/bcr-2013-200378
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Unusual aetiology of isolated lower motor neuron facial palsy: systemic lupus erythematosus presenting with cranial nerve palsy and nephritis

Abstract: A 20-year-old woman presented with common cold symptoms was found to have a left-sided facial droop. On examination, peripheral facial nerve palsy was confirmed. Subsequent testing showed nephrotic range proteinuria and positive serologies including antinuclear antibody and anti-smith antibody. Kidney biopsy showed stage III lupus nephritis. Treatment with pulse steroids along with mycophenolate mofetil for her lupus nephritis resulted in concomitant improvement of her facial palsy.

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Cited by 7 publications
(3 citation statements)
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“…Another peculiar finding in this case was the bilateral lower motor neuron-type facial paresis, an uncommon peripheral neuraxial manifestation of neuropsychiatric syndromes of SLE. 20 , 21 The pathophysiology of the lower motor neuron-type facial paresis in SLE might be the same as that of myelitis. 2 - 7 , 9 , 10 Herein, thrombotic microvascular occlusion caused by antiphospholipid antibodies was considered as a possibility 20 , 21 ; however, the rapid recovery following rituximab therapy does not support this hypothesis.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Another peculiar finding in this case was the bilateral lower motor neuron-type facial paresis, an uncommon peripheral neuraxial manifestation of neuropsychiatric syndromes of SLE. 20 , 21 The pathophysiology of the lower motor neuron-type facial paresis in SLE might be the same as that of myelitis. 2 - 7 , 9 , 10 Herein, thrombotic microvascular occlusion caused by antiphospholipid antibodies was considered as a possibility 20 , 21 ; however, the rapid recovery following rituximab therapy does not support this hypothesis.…”
Section: Discussionmentioning
confidence: 99%
“… 20 , 21 The pathophysiology of the lower motor neuron-type facial paresis in SLE might be the same as that of myelitis. 2 - 7 , 9 , 10 Herein, thrombotic microvascular occlusion caused by antiphospholipid antibodies was considered as a possibility 20 , 21 ; however, the rapid recovery following rituximab therapy does not support this hypothesis. Furthermore, spinal artery thrombosis-related myelitis was ruled out because of the absence of any characteristic pain and imaging abnormalities in this index case.…”
Section: Discussionmentioning
confidence: 99%
“…A recent review of NPSLE indicated that cranial neuropathy is a rare manifestation (0.5–1%) [4]. Several dozen case reports on peripheral cranial nerve palsy have been reported in patients with SLE [57].…”
Section: Introductionmentioning
confidence: 99%