Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5912658 | Multiple Sclerosis and Related Disorders | 2015 | 4 Pages |
Abstract
Longitudinally extensive transverse myelitis (LETM) is most commonly associated with neuromyelitis optica spectrum disorders (NMOSD). However, a wide range of etiologies may produce longitudinally extensive spinal cord lesions (LESCLs) on imaging. We highlight the case of a patient with a spinal cord tumor whose imaging showed LESCL and was diagnosed with LETM. He did not respond to immunosuppression and subsequently developed a progressive and protracted clinical course. Thoracic cord biopsy performed 6 years after symptom onset showed primary spinal oligoastrocytoma. We discuss the features that should raise suspicion of a neoplasm in the context of LESCL and serve a reminder that not all LESCLs are inflammatory.
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Authors
T.R. Yeo, C.F. Wong, J.J.X. Lee, V.Z.Y. Ng, K. Tan,