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Published on: October 25, 2018
Postinfectious myasthenia gravis: report of two children
Kevin J Felice1, Francis J DiMario, Stephen R Conway
1Department of Neurology, University of Connecticut School of Medicine, Farmington, CT 06030-1840, USA. felice@nso.uchc.edu
Insights
Transient myasthenia gravis can occur in children following viral infections. Symptoms resolved spontaneously, suggesting a temporary immune response possibly triggered by molecular mimicry.
Area of Science:
- Neurology
- Immunology
- Pediatrics
Background:
- Myasthenia gravis (MG) is a rare autoimmune disorder affecting neuromuscular junctions.
- Viral infections are increasingly recognized as potential triggers for autoimmune conditions.
- Transient forms of MG, particularly in children, warrant further investigation.
Observation:
- Two pediatric cases of transient myasthenia gravis following viral illnesses are presented.
- Case 1: A 5-year-old boy with oculobulbar weakness post-varicella-zoster infection.
- Case 2: A 4-year-old boy with facial diplegia and dysarthria post-viral pharyngitis.
Findings:
- Diagnosis of myasthenia gravis confirmed by electrophysiological studies and clinical response to pyridostigmine.
- Both patients experienced gradual symptom resolution and no recurrence after pyridostigmine withdrawal.
- Suggests a transient autoimmune process, potentially linked to viral triggers.
Implications:
- Viral infections may precipitate a temporary autoimmune response targeting the acetylcholine receptor.
- Molecular mimicry is a plausible mechanism for this pediatric MG variant.
- Understanding this link can inform diagnosis and management of post-viral neurological complications.
Abstract:
We report two children with transient myasthenia gravis preceded by viral illnesses. The first is a 5-year-old boy who developed oculobulbar weakness 2 weeks following a varicella-zoster infection. The second is a 4-year-old boy who developed facial diplegia and dysarthria several weeks following a viral pharyngitis. Myasthenia gravis was diagnosed based on the substantial decremental changes on 3 Hz repetitive motor nerve stimulation studies for the first child and on the positive edrophonium test and complete improvement in symptoms during pyridostigmine therapy for both children. In both cases, the symptoms gradually resolved and have not recurred following discontinuation of pyridostigmine. Molecular mimicry between the acetylcholine receptor and viral proteins might provide the nidus for the immune response in this variant of myasthenia gravis.
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