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- Acute disseminated encephalomyelitis
- filariasis
- Wuchereria bancrofti
- neuroimmunology
- myopathy
- adrenoleucodystrophy
- Parkinson's disease
- speech therapy
- paediatric neurology
- neuromuscular
- EMG (single fibre)
- HMSN (charcot-marie-tooth)
- immunology
- Lambert–Eaton syndrome
- CIDP
- myasthenia
- myelin
- Guillain–Barré syndrome
- channels
- dystrophin
- FSH
- mitochondrial disorders
- muscle disease
Introduction
Acute disseminated encephalomyelitis (ADEM) is thought to be an autoimmune inflammatory demyelinating disorder of the central nervous system (CNS) that occurs within weeks of a preceding viral illness, vaccination or, rarely, a bacterial infection. ADEM is less well known after a helminth infection and, in fact, filarial infection is known to provide protection against demyelinating CNS disease like multiple sclerosis.1 We present a patient who developed ADEM following acute filarial infection of the left arm. We also discuss the possible immunological mechanisms that led to ADEM following an acute filarial infection in our patient.
Case report
A 38-year-old man had acute onset weakness of left upper and lower limbs that progressed over the next 2–3 days resulting in loss of ambulation. There was no associated headache, vomiting, fever or seizures. Two months ago, the patient had developed acute painful swelling of his left arm with redness of overlying skin in the axilla and medial upper arm along with fever that lasted for 7 days. Gradually, his arm swelling and pain reduced after taking self-administered anti-inflammatory drugs. Several painless beaded swellings remained in the medial aspect of his left upper arm. On examination, there was a tense, warm, round, non-tender swelling of 3 cm diameter in the medial left arm with normal overlying …
Footnotes
Competing interests None.
Provenance and peer review Not commissioned; externally peer reviewed.