SciELO - Scientific Electronic Library Online

 
vol.38 número4Síndrome de Tolosa-Hunt una extraña causa de oftalmoplejía dolorosa: reporte de casoAfasia primaria progresiva y sus variantes: diagnóstico, evolución, características imagenológicas y manejo índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • En proceso de indezaciónCitado por Google
  • No hay articulos similaresSimilares en SciELO
  • En proceso de indezaciónSimilares en Google

Compartir


Acta Neurológica Colombiana

versión impresa ISSN 0120-8748versión On-line ISSN 2422-4022

Resumen

CACERES GONZALEZ, Juan David et al. Progressive multifocal leukoencephalopathy: severe disease in the immunosuppressed patient. Case report. Acta Neurol Colomb. [online]. 2022, vol.38, n.4, pp.224-229.  Epub 02-Feb-2023. ISSN 0120-8748.  https://doi.org/10.22379/24224022431.

INTRODUCTION:

Patients with immunocompromised or weakened immune system can develop a disabling and even life-threatening neurological disorder such as progressive multifocal leukoencephalopathy (PML) caused by John Cunningham (JC) virus.

CASE PRESENTATION:

We present the case of a 26-year-old man with a recent diagnosis of human immunodeficiency virus (HIV) infection who presented constitutional symptoms, progressive neurological deficit due to left spastic hemiparesis with decreased visual acuity and behavioral changes. The brain Magnetic Resonance Imaging (MRI) showed diffuse subcortical involvement of the white matter including the U-fibers, which, correlated with a detection of JC virus DNA by polymerase chain reaction (PCR) cerebrospinal fluid, confirmed the diagnosis of PML.

DISCUSSION:

PML can range from subtle cognitive impairment imperceptible to the clinician to sensory-motor deficits and visual disturbances that can be corroborated in MRI by identifying the typical lesions in the white matter or by detecting the virus by PCR in cerebrospinal fluid. The specific management of the cause that triggered the immunosuppression continues to be the mainstay of treatment.

CONCLUSION:

At the minimum diagnostic suspicion in patients with risk factors and clinical manifestations consistent with the disease should proceed to confirm the diagnosis and promptly immune reconstitution.

Palabras clave : Immunocompromised host, Leukoencephalopathy, Progressive Multifocal; JC virus; HIV (MeSH).

        · resumen en Español     · texto en Español     · Español ( pdf )