Abstract
IgG4-related disease (IgG4-RD) is a rare and often misdiagnosed disorder with limited literature that highlights the different neurological presentations of this treatable disease. The diagnosis of IgG4-RD could be challenging, while imaging is fundamental for the diagnosis, biopsy is considered the gold standard. Most cases respond well to steroids and immunosuppressive therapy. This is a case series study that illustrates the varied neurological presentations of IgG4-RD through three different patients that were followed at the Montreal Neurological Institute. This paper takes you through the diagnostic strategy that we followed to accurately diagnose and treat those patients.
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Abbas, G., Karamchandani, J., Ciarallo, A., & Durcan, L. (2023). IgG4-Related Disease of the Central Nervous System: A Case Series. Canadian Journal of Neurological Sciences, 50(6), 907–913. https://doi.org/10.1017/cjn.2022.321
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