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Thoracic intramedullary chordoma without bone involvement: a rare clinical entity.
Faheem, Mohd; Zeeshan, Qazi; Ojha, Balkrishna; Agrawal, Preeti.
Afiliação
  • Faheem M; Department of Neurosurgery, King George's Medical University, Lucknow, Uttar Pradesh, India.
  • Zeeshan Q; Department of Neurosurgery, King George's Medical University, Lucknow, Uttar Pradesh, India.
  • Ojha B; Department of Neurosurgery, King George's Medical University, Lucknow, Uttar Pradesh, India.
  • Agrawal P; Department of Pathology, King George's Medical University, Lucknow, Uttar Pradesh, India.
BMJ Case Rep ; 20162016 Jul 28.
Article em En | MEDLINE | ID: mdl-27469385
An 8-year-old boy presented with a 1-year history of low backache, followed by paraparesis and urinary incontinence. MRI of the thoracic spine revealed an intramedullary, intensely contrast-enhancing lesion extending from T11 to L1 vertebral level, consistent with astrocytoma, ependymoma or haemangioblastoma. A diagnosis of intramedullary chordoma was made on tissue biopsy and immunohistochemical study. This is the second report of an intramedullary chordoma without bone involvement in English literature. After 6 months of follow-up, patient showed good clinical outcome in terms of improvement in power in lower limbs and backache.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Medula Espinal / Cordoma Tipo de estudo: Diagnostic_studies Limite: Child / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Medula Espinal / Cordoma Tipo de estudo: Diagnostic_studies Limite: Child / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article