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Progressive multifocal leukoencephalopathy


This page is about clinical aspects of the disease.  For microbiologic aspects of the causative organism(s), see JC virus.

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Progressive multifocal leucoencephalopathy, Multifocal leucoencephalopathy, Multifocal leukoencephalopathy, PML, PMLE

Patients with Progressive Multifocal leukoencephalopathy(PML) have a long-term neurological sequelae and is often fatal. The mortality rate is 30%-50% [1] in early months of diagnosis. Those who are immunocompromised are at significant risk of reactivation.

COMPLICATIONS

PML may complicate into the following :

  • Neurologic Dysfunction
  • Dementia
  • Blindness
  • Seizures
PROGNOSIS
  • The prognosis is variable and depends on the underlying severity of PML.
  • Impairment of immune system (eg. HIV) or use of immunosuppressants may worsen prognosis and leads to rapid progression of the disease.[1]
  • Patients who survive have substantial morbidity and severe neurological disabilities.[2]

Reference

  1. Progressive Multifocal Leukoencephalopathy Information Page. NIH-National Institute of Neurological Disorders and Stroke. 29 July 2019. Retrieved 12 June 2021.
  2. Castle, D., & Robertson, N. P. (2019). Treatment of progressive multifocal leukoencephalopathy. Journal of Neurology, 266(10), 2587–2589. https://doi.org/10.1007/s00415-019-09501-y

History and Symptoms | Physical Examination | Laboratory Findings | X Ray | CT | MRI | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies

Treatment

Medical Therapy | Surgery | Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies

Case Studies

Case #1

Template:Viral diseases de:Progressive multifokale Leukenzephalopathie nl:Progressieve multifocale leukoencefalopathie


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