Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study

J Inherit Metab Dis. 1998 Aug;21(6):639-44. doi: 10.1023/a:1005428432730.

Abstract

A 16-month-old boy was hospitalized because of a 1-day history of severe ketoacidosis with lethargy, hypotonia, vomiting, and important dyspnoea. Organic acid assay by gas chromatography-mass spectrometry confirmed the diagnosis of methylmalonic acidaemia (MMA). On the sixteenth day, he developed an acute extrapyramidal disorder. The CT scan of the brain disclosed bilaterally symmetric lucency of basal ganglia. He died at 17 months of age. Post-mortem neuropathological examination, showed severe necrosis with spongiosis, cystic cavitation and numerous lipid-laden macrophages of the globi pallidi, and mild spongiosis of subthalamic nuclei, mammillary bodies, portion of internal capsule adjacent to globus pallidus, superior cerebellar peduncles and tegmentum of brainstem. Pallidal infarction, a focal ischaemic lesion, demonstrates that ischaemia/energy depletion may be important in the etiology of the neuropathology of MMA.

Publication types

  • Case Reports

MeSH terms

  • Cobamides / deficiency
  • Fatal Outcome
  • Globus Pallidus / pathology*
  • Humans
  • Infant
  • Male
  • Metabolism, Inborn Errors / diagnosis
  • Metabolism, Inborn Errors / enzymology
  • Metabolism, Inborn Errors / pathology*
  • Methylmalonic Acid / blood*
  • Methylmalonic Acid / cerebrospinal fluid
  • Methylmalonic Acid / urine
  • Methylmalonyl-CoA Mutase / deficiency

Substances

  • Cobamides
  • Methylmalonic Acid
  • Methylmalonyl-CoA Mutase
  • cobamamide