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Toe walking after three: how serious could it be?
Ustaris, Linda-Marie; Seidman, Roberta; Bindra, Tejwant; Basak, Ratna.
Afiliação
  • Ustaris LM; Med-Peds, Stony Brook University Hospital, Stony Brook, New York, USA.
  • Seidman R; Department of Pathology, Stony Brook University Hospital, Stony Brook, New York, USA.
  • Bindra T; Department of Neurology, Stony Brook University Hospital, Stony Brook, New York, USA.
  • Basak R; Department of Pediatrics, Stony Brook University Hospital, Stony Brook, New York, USA.
BMJ Case Rep ; 20182018 May 30.
Article em En | MEDLINE | ID: mdl-29848524
ABSTRACT
A 4-year-old girl with no significant medical or family history presented with toe walking, leg pain, unsteady gait and frequent falls for 2 months. Examination revealed upper motor neuron signs in the lower extremities. Laboratory tests were normal including creatinephosphokinase and lactate dehydrogenase. Brain and lumbar spine MRI were normal. MRI cervical and thoracic spine showed a large intradural and extradural mass arising from the right C7 nerve root, widening of the neural canal with evidence of cord compression. She underwent C6-C7 laminectomy with excision of the tumour. Pathology revealed spindle cell tumour with extensive expression of S100 protein and CD56, with Ki-67 proliferation index of 1%-2% consistent with benign schwannoma. She made an excellent recovery following surgery and physiotherapy sessions. Review of literature shows rare reported case of schwannoma prior to the third decade of life.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Medula Espinal / Transtornos Neurológicos da Marcha / Neurilemoma Tipo de estudo: Etiology_studies Limite: Child, preschool / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Medula Espinal / Transtornos Neurológicos da Marcha / Neurilemoma Tipo de estudo: Etiology_studies Limite: Child, preschool / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article