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| Posterior leukoencephalopathy syndrome | |
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| The first 150 words of the full text of this article appear below. |
EDITOR,
I read with interest the excellent review
on posterior leukoencephalopathy syndrome published in
January.1 The author, however, has omitted an important
differential diagnosis in his article
namely, progressive multifocal
leukoencephalopathy (PML). This can mimic the appearances of posterior
leukoencephalopathy on both computed tomography and magnetic resonance
imaging (MRI) scans of the brain and needs to be high on the
differential diagnosis especially in patients with AIDS.2
PML was first described in 19583 and is characterised by
widespread demyelination in the cerebral hemispheres. Today PML is seen
most frequently in patients with AIDS but can also occur in patients
with chronic neoplasia and immunosuppressed states. Intellectual
changes, hemiparesis, visual field defects, ataxia, aphasia, and
dementia are clinical features. Seizures are rare. The cerebrospinal
fluid is usually normal. On computed tomography there may be low
attenuation areas in the posterior fossae but MRI (T2 weighted) shows
characteristic increased signal
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