Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesis.

Abstract

Infantile Alexander disease is a rare progressive leukodystrophy caused by autosomal dominant mutations in the (GFAP) gene typically presenting with psychomotor retardation, progressive macrocephaly and refractory epilepsy. Neuroradiological hallmarks are extensive white matter lesions with frontal preponderance as well as signal intensity changes of basal ganglia and medulla oblongata with variable contrast enhancement. Here, we report an atypical manifestation in a 21-month-old boy presenting with flaccid paraparesis and areflexia. Cognitive, visual as well as fine motor skills and muscular strength of the upper extremities were appropriate for age. Weight and height as well as head circumference were within normal range. Clinical or electroencephalographic signs of seizures were absent. Cranial MRI demonstrated bifrontal cystic tumorous lesions with partial contrast rims, as well as space-occupying focal lesions of the caudate nuclei. Spinal MRI revealed swelling of the lumbar and cervical spinal cord. CSF and blood chemistry showed normal results. Histopathology of a subcortical lesion showed large amounts of Rosenthal fibers and protein droplets characteristic of Alexander disease. Sequencing detected a heterozygous mutation of the GFAP gene (c.205G > A; p.(Glu69Lys)) that has been reported before as probably pathogenetic in another case of lower spinal involvement. This well documented case draws attention to atypical spinal manifestations of Alexander disease and gives histopathological proof of the pathogenetic role of a rare GFAP mutation with marked spinal involvement.

• Authors: Florian Brackmann, Roland Coras, Karl Rössler, Cornelia Kraus, Oliver Rompel, Regina Trollmann
• Journal: Brain & development (Brain Dev) Vol. 40 Issue 4 Pg. 330-333 (Apr 2018) ISSN: 1872-7131 [Electronic] Netherlands
• PMID: 29191363 (Publication Type: Case Reports, Journal Article)
• Copyright: Copyright © 2017 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.

Chemical References

• Glial Fibrillary Acidic Protein

Topics

• Alexander Disease (diagnostic imaging, genetics, pathology)
• Brain (diagnostic imaging, pathology)
• Diagnosis, Differential
• Glial Fibrillary Acidic Protein (genetics)
• Humans
• Infant
• Male
• Mutation
• Paraparesis (diagnostic imaging, genetics, pathology)
• Spinal Cord (diagnostic imaging)