[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 34.238.190.122. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Observation
April 2010

Is It ADEM, POLG, or Both?

Author Affiliations

Author Affiliations: Department of Neurology, Division of Pediatric Neurology (Drs Harris, Walsh, and Golomb), and Department of Pathology and Laboratory Medicine (Dr Hattab), Indiana University School of Medicine, Indianapolis.

Arch Neurol. 2010;67(4):493-496. doi:10.1001/archneurol.2010.36
Abstract

Objective  To describe a child with apparent brain biopsy–confirmed acute disseminated encephalomyelitis (ADEM) but genetic confirmation of compound heterozygosity for DNA mutations of the polymerase γ (POLG) gene.

Design  Case report.

Setting  Tertiary referral center.

Patient  A 4-year-old boy presented with ataxia and encephalopathy.

Results  Magnetic resonance imaging demonstrated multiple focal areas of T2 prolongation. The patient's family refused steroid treatment. His symptoms improved then progressed. Magnetic resonance imaging findings also progressed. A cerebrospinal fluid specimen revealed myelin basic protein and oligoclonal bands. A brain biopsy specimen demonstrated demyelination, suggesting progression of ADEM. However, polymerase chain reaction amplification and sequencing revealed 2 heterozygous mutations of the POLG gene, suggesting mitochondrial disease. The patient died 9 months after his initial presentation.

Conclusions  This case raises interesting questions about whether ADEM triggered severe neurologic degeneration in a patient with mitochondrial disease, whether mitochondrial disease predisposed to a pathologic immune response, or whether mitochondrial disease can mimic an autoimmune disease. Mitochondrial disease–causing mutations may help explain the poor outcome in some cases of apparent autoimmune central nervous system disease.

×