Progressive multifocal leukoencephalopathy developed in incomplete Heerfordt syndrome, a rare manifestation of sarcoidosis, without steroid therapy responding to cidofovir

Clin Neurol Neurosurg. 2010 Feb;112(2):153-6. doi: 10.1016/j.clineuro.2009.10.005. Epub 2009 Nov 4.

Abstract

Progressive multifocal leukoencephalopathy (PML) is a severe demyelinating disease of the central nervous system caused by the JC virus; the mortality rate is high and it is usually refractory to treatment. In non-HIV patients, PML occurs as a late consequence of hematologic malignancies or during prolonged immunosuppression for transplantation or autoimmune disease. We describe a 34-year-old PML patient with incomplete Heerfordt syndrome, a rare type of sarcoidosis, who had not received any immunosuppressants, including steroids, at the onset and who was clinically and radiologically responsive to the antiviral drug cidofovir.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antiviral Agents / therapeutic use*
  • Cidofovir
  • Cytosine / analogs & derivatives*
  • Cytosine / therapeutic use
  • Humans
  • Leukoencephalopathy, Progressive Multifocal / diagnostic imaging
  • Leukoencephalopathy, Progressive Multifocal / etiology*
  • Male
  • Organophosphonates / therapeutic use*
  • Parotid Gland / diagnostic imaging
  • Radiography
  • Sarcoidosis / diagnostic imaging
  • Sarcoidosis / drug therapy*
  • Treatment Outcome
  • Uveoparotid Fever / complications*
  • Uveoparotid Fever / diagnostic imaging

Substances

  • Antiviral Agents
  • Organophosphonates
  • Cytosine
  • Cidofovir