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Myelopathy associated with intrathecal methotrexate
  1. Pedro Gustavo Barros Rodrigues1,
  2. Talles Tavares de Lima2,
  3. Fernando Barroso Duarte3,4,
  4. Paulo Ribeiro Nóbrega1
  1. 1 Division of Neurology, Department of Clinical Medicine, Universidade Federal do Ceará, Fortaleza, Ceará, Brazil
  2. 2 Department of Clinical Medicine, Hospital Universitário Lauro Wanderley, João Pessoa, Paraíba, Brazil
  3. 3 Department of Surgery, Universidade Federal do Ceará, Fortaleza, Ceará, Brazil
  4. 4 Division of Cell Processing, Centro de Hematologia e Hemoterapia do Ceara, Fortaleza, Ceará, Brazil
  1. Correspondence to Pedro Gustavo Barros Rodrigues, Division of Neurology, Department of Clinical Medicine, Universidade Federal do Ceará, Fortaleza, Ceará 60430-160, Brazil; gustavo.rodrigues675{at}


A 21-year-old man developed progressive and bilateral lower limb numbness, gait impairment and urinary incontinence over 10 days. He had received intrathecal methotrexate 20 days previously for acute lymphoblastic B-cell leukaemia, following 7 months of systemic chemotherapy. MR scan of the spinal cord showed bilateral symmetric and extensive T2/fluid attenuated inversion recovery (FLAIR) increased signal involving the dorsal columns in the thoracic cord. His serum folate concentration was at the lower end of the normal range. We stopped the intrathecal chemotherapy and gave folate; after a few days, he progressively improved. Myelopathy is an important adverse effect of intrathecal methotrexate, which may cause clinical and imaging features resembling subacute combined degeneration of the spinal cord. CNS infiltration must be excluded, intrathecal chemotherapy stopped and deficiency of folate or vitamin B12 treated as appropriate.

  • myelopathy
  • clinical neurology
  • haematology
  • neurooncology

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  • Contributors Conception of the work—PGBR, TTdL and PRN. Drafting the work—PGBR, TTdL and PRN. Acquisition of the data—TTdL and FBD. Analysis and interpretation of data for the work—all authors. Design of the work—FBD and PRN. Revising the work critically—FBD and PRN. Final approval of the version to be published and agreement to be accountable for all aspects of the work—all authors.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned. Externally peer reviewed by Jeremy Rees, London.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.

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