Thoracic intramedullary chordoma without bone involvement: A rare clinical entity

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Abstract

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.

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APA

Faheem, M., Zeeshan, Q., Ojha, B., & Agrawal, P. (2016). Thoracic intramedullary chordoma without bone involvement: A rare clinical entity. BMJ Case Reports, 2016. https://doi.org/10.1136/bcr-2016-216101

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