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1.
J Neurooncol ; 103(3): 771-6, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20941525

RESUMO

Herpes simplex encephalitis (HSE) is a rare complication of neurosurgical procedures but must be considered in early deterioration of the postoperative patient. This is the first report of HSE following spinal cord tumor resection. A 65-year-old woman had C2-C5 laminectomy for subtotal resection of intramedullary ependymoma. Six days postoperatively she developed fever, vomiting and rapid decline in mental status. Brain MRI revealed enhancement of left insular cortex. Polymerase chain reaction on cerebrospinal fluid (CSF) identified herpes simplex virus type 1 (HSV-1) as the causal agent. Twenty-one days of acyclovir led to improvement. Three subsequent admissions to neurological intensive care unit were required for deterioration in mental status, including pneumonia, hydrocephalus and deep vein thromboses. Ventriculoperitoneal shunt (VPS), tracheotomy, percutaneous intravenous central catheter (PICC) line and percutaneous endoscopic gastrostomy (PEG) were placed. She was discharged to skilled nursing home care. Acyclovir is effective therapy against HSV, though outcomes may be poor even in optimally treated cases. Empiric treatment must be started even in the absence of serologic evidence of HSV infection if suspicion for HSE is high.


Assuntos
Encefalite por Herpes Simples/etiologia , Procedimentos Neurocirúrgicos/efeitos adversos , Idoso , Encefalite por Herpes Simples/líquido cefalorraquidiano , Ependimoma/cirurgia , Feminino , Herpes Simples/líquido cefalorraquidiano , Humanos , Imageamento por Ressonância Magnética , Neoplasias da Coluna Vertebral/cirurgia , Derivação Ventriculoperitoneal/efeitos adversos , Derivação Ventriculoperitoneal/métodos
2.
J Neuroimmunol ; 127(1-2): 145-8, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12044986

RESUMO

We tested patients with celiac disease (CD) for the presence of serum anti-ganglioside antibodies. Six of twenty-seven patient sera were reactive against brain gangliosides by an agglutination immunoassay. Neurological examination in all six revealed the presence of distal sensory loss, consistent with the diagnosis of peripheral neuropathy. When tested by ELISA for antibodies to isolated GM1, GM2, GD1a, GD1b, GT1b, and GQ1b gangliosides, all six were positive for IgG antibodies to at least one. The neuropathy of celiac disease may be autoimmune and associated with anti-ganglioside antibodies. The presence of IgG reactivity furthermore implicates a T cell-mediated response to ganglioside antigens.


Assuntos
Autoanticorpos/sangue , Doença Celíaca/imunologia , Gangliosídeos/imunologia , Doenças do Sistema Nervoso Periférico/imunologia , Adulto , Idoso , Doença Celíaca/complicações , Feminino , Humanos , Imunoglobulina A/sangue , Imunoglobulina G/sangue , Imunoglobulina M/sangue , Masculino , Pessoa de Meia-Idade , Doenças do Sistema Nervoso Periférico/etiologia
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