Chronicle of a Foretold Intersection: Mycoplasma pneumoniae and Brown- Séquard Syndrome

Authors

  • Catarina Tavares Pediatrics Department, Unidade Local de Saúde de Viseu Dão-Lafões, Viseu, Portugal; Center for Child Development – Neuropediatrics Unit, Hospital Pediátrico, Unidade Local de Saúde de Coimbra, Coimbra, Portugal https://orcid.org/0009-0002-3502-5876
  • Mariana Costa Pediatrics Department, Hospital Pediátrico, Unidade Local de Saúde de Coimbra, Coimbra, Portugal https://orcid.org/0000-0003-4501-0192
  • Joana Pinto Medical Image Department – Neuroradiology Unit, Unidade Local de Saúde de Coimbra, Coimbra, Portugal https://orcid.org/0000-0001-7783-8440
  • Joana Amaral Center for Child Development – Neuropediatrics Unit, Hospital Pediátrico, Unidade Local de Saúde de Coimbra, Coimbra, Portugal https://orcid.org/0000-0002-8892-0551
  • Filipe Palavra Center for Child Development – Neuropediatrics Unit, Hospital Pediátrico, Unidade Local de Saúde de Coimbra, Coimbra, Portugal; Laboratory of Pharmacology and Experimental Therapeutics, Coimbra Institute for Clinical and Biomedical Research (iCBR), Faculty of Medicine, Coimbra University, Coimbra, Portugal; Clinical Academic Center of Coimbra (CACC), Coimbra, Portugal https://orcid.org/0000-0002-2165-130X

DOI:

https://doi.org/10.46531/sinapse/CC/198/2026

Keywords:

Brown-Séquard Syndrome/etiology, Child, Mycoplasma pneumoniae, Pneumonia, Mycoplasma/complications

Abstract

Mycoplasma pneumoniae is a frequent cause of community-acquired respiratory infection in children but can also produce neurological complications. We report a 9-year-old child who developed neck pain followed by right hemiparesis and contralateral sensory loss, compatible with a Brown-Séquard-like presentation. Brain imaging was normal; spinal magnetic resonance imaging (MRI) showed a focal, right-lateral, C2–C4 T2-hyperintense lesion without contrast enhancement, consistent with myelitis. Respiratory multiplex PCR and serology supported recent M. pneumoniae infection. The patient improved substantially after corticosteroids, targeted antibiotics and rehabilitation, with near-complete functional recovery and no recurrence of disease. Serum MOG-IgG and AQP4-IgG were negative, and neuroimaging did not reveal features typical of MOGAD or NMOSD, helping exclude primary demyelinating disease. This case highlights M. pneumoniae myelitis presenting as a Brown-Séquard syndrome in childhood and underscores the importance of a structured differential diagnosis to guide timely and etiology-specific management.

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References

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Published

2026-03-19

How to Cite

1.
Tavares C, Costa M, Pinto J, Amaral J, Palavra F. Chronicle of a Foretold Intersection: Mycoplasma pneumoniae and Brown- Séquard Syndrome. Sinapse [Internet]. 2026 Mar. 19 [cited 2026 Mar. 27];. Available from: https://sinapse.pt/index.php/journal/article/view/198

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Case Reports

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