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  Vol. 62 No. 4, April 2005 TABLE OF CONTENTS
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L-2-Hydroxyglutaric Aciduria

Clinical, Neuroimaging, and Neuropathological Findings

Manuel Seijo-Martínez, MD; Carmen Navarro, MD; Maria Castro del Río, MD; Oscar Vila, MD; Miguel Puig, MD; Antonia Ribes, PhD; Mercedes Butron, MD

Arch Neurol. 2005;62:666-670.

Background  L-2-Hydroxyglutaric aciduria is a rare, infantile-onset, autosomal recessive organic aciduria affecting exclusively the central nervous system. To our knowledge, only 1 complete report of the neuropathological findings in an adult has been published.

Objective  To present the clinical, neuroimaging, and neuropathological findings of L-2-hydroxyglutaric aciduria.

Design  Case report.

Setting  Complexo Hospitalario de Pontevedra, Pontevedra, Spain.

Patient  A 15-year-old boy who had early infantile-onset progressive psychomotor regression, mild choreodystonia affecting the distal part of the upper limbs, pyramidal signs, and epilepsy.

Results  The diagnosis of L-2-hydroxyglutaric aciduria was confirmed by the finding of highly elevated levels of L-2-hydroxyglutaric acid in the serum, urine, and cerebrospinal fluid. The neuroimaging findings showed striking confluent subcortical white matter lesions and minimal basal ganglia (pallidum, thalamic, and putaminal) abnormalities. The patient died of a spontaneous mesenteric thrombosis. The postmortem neuropathological findings showed spongiosis and cystic cavitations in subcortical white matter, with minimal abnormalities of the basal ganglia. The dentate nucleus, a structure usually affected in neuroimaging studies, showed minimal neuronal loss but was surrounded by important spongiosis and microvacuolation with astrocytic proliferation.

Conclusions  This case reaffirms that L-2-hydroxyglutaric aciduria is a spongiform type of leukoencephalopathy with cystic cavitations predominating in the subcortical areas. Although the neuroimaging findings are highly characteristic of the disease, in this patient cerebellar abnormalities were minimal and dentate signal abnormalities were not present.


Author Affiliations: Departments of Neurology (Drs Seijo-Martínez and Castro del Río) and Radiology (Dr Puig), Complexo Hospitalario de Pontevedra, Pontevedra, Spain; Department of Neuropathology, Hospital Meixoeiro, Vigo, Spain (Dr Navarro); Department of Radiology, Instituto Galego de Medicina Tecnica (Dr Vila), and Pathology (Dr Butron), Hospital Xeral-Cies, Vigo; and Instituto de Bioquímica Clínica, Corporació Sanitaria Clínic, Barcelona, Spain (Dr Ribes).







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