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CASE REPORT
Tumefactive demyelination: an unusual cause of a spontaneously resolving homonymous hemianopia
  1. R A Dwivedi1,
  2. R E Dwivedi1,
  3. J M Durnian1,
  4. C A Young2
  1. 1Royal Liverpool & Broadgreen University Hospitals Trust, Liverpool, UK
  2. 2The Walton Centre NHS Foundation Trust, Fazakerley, Liverpool, UK
  1. Correspondence to Dr Rahul Dwivedi, r.dwivedi{at}doctors.org.uk

Summary

A 21-year-old man presented to eye casualty complaining of altered vision associated with headache and vomiting upon waking. Clinical examination was unremarkable except for a right-sided homonymous hemianopia. The MRI scan of the brain revealed a space occupying lesion within the occipital lobe and MR spectroscopy highlighted this to be inflammatory in nature, most likely a tumefactive demyelinating lesion (TDL). Lumbar puncture displayed positive oligoclonal bands. The patient was managed conservatively and made a full recovery, with normal visual fields recorded after a 3 month follow-up. This is a case of a TDL manifesting itself as an unusual cause of homonymous hemianopia; misdiagnosis of TDL is common and potentially damaging to the patient.

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