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Vitamin B12 deficiency mimicking neuroimaging features of motor neuron disease

Deficiência de vitamina B12 mimetizando aspectos de neuroimagem da doença do neurônio motor

A 45-year-old man presented with 2-month-history of progressive gait disturbances and behavioral changes. Examination showed vibration sense compromise and pyramidal signs of release. Blood test revealed low serum vitamin B12 (120 pg/mL; normal range>200 pg/mL). Brain MRI disclosed hyperintense signal in corticospinal tracts, a similar pattern observed in motor neuron disease (MND) (Figure). Replacement therapy was started and there were motor and cognitive improvements.

Figure
. (A) Axial T2-weighted and (B) axial FLAIR-weighted brain MRI disclosing multiple frontal hyperintense signal changes in corticospinal tracts projections, a similar pattern observed in motor neuron disease. (C) Axial MTC sequence is normal, and no contrast enhancement was observed.

Vitamin B12 deficiency may present with different neurological syndromes 1. Kalita J, Misra UK. Vitamin B12 deficiency neurological syndromes: correlation of clinical, MRI and cognitive evoked potential. J Neurol 2008;255:353-359. . Encephalopathy related to B12 deficiency presents with nonspecific white matter changes 2. Sudo K, Tashiro K. Cerebral white matter lesions associated with vitamin B12 deficiency. Neurology 1998;51:325-326. . Although MTC brain MRI sequence was normal, our patient presented neuroimaging features observed in MND 3. Lee YC, Markus R, Hughes A. MRI in ALS: corticospinal tract hyperintensity. Neurology 2003;61:1600. .

References

  • 1
    Kalita J, Misra UK. Vitamin B12 deficiency neurological syndromes: correlation of clinical, MRI and cognitive evoked potential. J Neurol 2008;255:353-359.
  • 2
    Sudo K, Tashiro K. Cerebral white matter lesions associated with vitamin B12 deficiency. Neurology 1998;51:325-326.
  • 3
    Lee YC, Markus R, Hughes A. MRI in ALS: corticospinal tract hyperintensity. Neurology 2003;61:1600.

Publication Dates

  • Publication in this collection
    Jan 2014

History

  • Received
    15 July 2013
  • Accepted
    23 July 2013
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