Abstract
Autoimmune autonomic ganglionopathy is an autonomic disorder that occurs as a symptom of paraneoplastic neurological syndrome. To date, there have been no reports on multiple myeloma with autoimmune autonomic ganglionopathy. A 37-year-old Japanese woman suffered from orthostatic hypotension was diagnosed with multiple myeloma (IgG kappa type), and a serological examination revealed the presence of anti-ganglionic nicotinic acetylcholine receptor (anti-gAChR) antibodies. She was treated for multiple myeloma, as a result, the autonomic disturbance improved and her anti-gAChR antibody titer decreased to undetectable levels, despite the fact that she only achieved a partial remission of multiple myeloma. Treatment for multiple myeloma may improve autoimmune autonomic ganglionopathy.
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Nakae, Y., Hyuga, M., Terada, Y., Kishimoto, W., Fukunaga, A., Tabata, S., … Arima, N. (2017). Multiple myeloma presenting with autoimmune autonomic ganglionopathy. Internal Medicine, 56(24), 3347–3351. https://doi.org/10.2169/internalmedicine.9096-17
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