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Inmunohistoquímica de los cambios degenerativos del sistema nervioso central en paraparesias esp sticas asociadas al virus linfotrópico humanoTtipol(HTLV-l) / Immunohistochemistry of degenerative changes in the central nervous system in spastic paraparesis associated to human T lymphotropic virus type I (HTLV-I)
Cartier R., Luis; Vergara R., Carmen; Valenzuela P., María Antonieta.
Afiliação
  • Cartier R., Luis; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas. Santiago. CL
  • Vergara R., Carmen; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas. Santiago. CL
  • Valenzuela P., María Antonieta; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas. Santiago. CL
Rev. méd. Chile ; 135(9): 1139-1146, sept. 2007. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-468202
Biblioteca responsável: BR1.1
ABSTRACT

Background:

Human T lymphotropic virus type I is associated with tropical spastic paraparesis, that is a chronic and progressive disease which damages specially the cortiespinal tracts. The pathogenesis of this degenerative process remains unknown.

Aim:

To identify histopathological aspects that could suggest a pathogenic hypothesis we studied immunohistochemical features in spinal cords obtained from patients that died due to progressive spastic paraparesis. Patients and

Methods:

Five males and five females, who died between 1990 and 2000, with a mean age of 52 years and mean disease duration of 8.6, were studied. All had a complete clinical and virological diagnosis. Samples were obtained from the frontal motor cortex and spinal cord (cervical, dorsal and lumbar segments), were fixed in formol (10 percent), included in paraffin, and stained with Haematoxylin and Luxol-fast-blue. Immunohistochemical study was made with anti-neurofilament antibodies 1100 (M0762, DAKO), anti-APP 120 (Rabbit Pre Amyloid protein 51-2700 ZYMED), anti-tau 1100 (A0024DAKO) and anti-ubiquitine 150 (NCL UBIQm Novocastra).

Results:

All cases had demyelinization and axonal loss in the cortico-spinal tracts; distal and segmental demyelinization of Goll tract; axonal thickening, amyloid precursor protein deposits in the white matter; tau protein aggregation in the spinal cord oligodendrocytes; axonal ubiquitination of sensitive and motor tracts, and subcortical white matter. Neurona! injury was absent.

Conclusions:

The systematic damage of motor and sensitive tracts of the spinal-cord and the absence of neurona! damage, defines a degenerative process limited to axons. This central axonopathie could be caused by a disturbance of axoplasmic transport.
Assuntos

Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Medula Espinal / Vírus Linfotrópico T Tipo 1 Humano / Paraparesia Espástica Tropical / Degeneração Neural Tipo de estudo: Estudo prognóstico / Fatores de risco Limite: Adulto / Idoso / Feminino / Humanos / Masculino Idioma: Espanhol Revista: Rev. méd. Chile Assunto da revista: Medicina Ano de publicação: 2007 Tipo de documento: Artigo / Documento de projeto País de afiliação: Chile Instituição/País de afiliação: Universidad de Chile/CL
Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Medula Espinal / Vírus Linfotrópico T Tipo 1 Humano / Paraparesia Espástica Tropical / Degeneração Neural Tipo de estudo: Estudo prognóstico / Fatores de risco Limite: Adulto / Idoso / Feminino / Humanos / Masculino Idioma: Espanhol Revista: Rev. méd. Chile Assunto da revista: Medicina Ano de publicação: 2007 Tipo de documento: Artigo / Documento de projeto País de afiliação: Chile Instituição/País de afiliação: Universidad de Chile/CL
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