Intravenous immunoglobulin treatment in a patient with adrenomyeloneuropathy

4Citations
Citations of this article
22Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Background: Adrenomyeloneuropathy (AMN) is one of several phenotypes of the adrenoleukodystrophy spectrum caused by mutations in the ABCD1 gene on the X chromosome. An inflammatory component is part of the disease complex ranging from severe childhood CNS demyelination to spinal cord and peripheral nerve degeneration.Case presentation: We present a patient with clinical progressive AMN and severe lower limb pain. Longitudinal brain magnetic resonance spectroscopy showed a constant slightly elevated myoinositol/total creatine ratio during the five year treatment period, probably reflecting demyelination, microglial activation and gliosis, indicating an inflammatory response. The pain was refractory to conventional therapy but intravenous immunoglobulin (IVIG) treatment was highly efficient.Conclusion: IVIG may be considered as a last resort for treatment of refractory pain in AMN patients with indications of an inflammatory component. © 2012 Jønch et al.; licensee BioMed Central Ltd.

Cite

CITATION STYLE

APA

Jønch, A. E., Danielsen, E. R., Thomsen, C., Meden, P., Svenstrup, K., & Nielsen, J. E. (2012). Intravenous immunoglobulin treatment in a patient with adrenomyeloneuropathy. BMC Neurology, 12. https://doi.org/10.1186/1471-2377-12-108

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free