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Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance
Autoimmune polyglandular syndrome (APS) causes autoimmune diseases of multiple organs and can also present with neurological symptoms. We here report a 58-year-old man who presented with progressive gait disturbance that had started 7 years ago. He had spasticity, reduced deep sensations, and trunca...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society of Internal Medicine
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400394/ https://www.ncbi.nlm.nih.gov/pubmed/36450465 http://dx.doi.org/10.2169/internalmedicine.0476-22 |
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author | Takeuchi, Yosuke Nomura, Toshiya Nakahara, Keiichi Ueda, Mitsuharu |
author_facet | Takeuchi, Yosuke Nomura, Toshiya Nakahara, Keiichi Ueda, Mitsuharu |
author_sort | Takeuchi, Yosuke |
collection | PubMed |
description | Autoimmune polyglandular syndrome (APS) causes autoimmune diseases of multiple organs and can also present with neurological symptoms. We here report a 58-year-old man who presented with progressive gait disturbance that had started 7 years ago. He had spasticity, reduced deep sensations, and truncal cerebellar ataxia. Laboratory examinations revealed autoantibody-related cobalamin deficiency and the presence of anti-thyroid antibodies and anti-glutamic acid decarboxylase antibodies. His gait worsened after cobalamin replenishment, but additional steroid therapy was effective. APS can cause refractory gait disturbance that requires not only cobalamin replenishment but also immunotherapy. |
format | Online Article Text |
id | pubmed-10400394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-104003942023-08-05 Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance Takeuchi, Yosuke Nomura, Toshiya Nakahara, Keiichi Ueda, Mitsuharu Intern Med Case Report Autoimmune polyglandular syndrome (APS) causes autoimmune diseases of multiple organs and can also present with neurological symptoms. We here report a 58-year-old man who presented with progressive gait disturbance that had started 7 years ago. He had spasticity, reduced deep sensations, and truncal cerebellar ataxia. Laboratory examinations revealed autoantibody-related cobalamin deficiency and the presence of anti-thyroid antibodies and anti-glutamic acid decarboxylase antibodies. His gait worsened after cobalamin replenishment, but additional steroid therapy was effective. APS can cause refractory gait disturbance that requires not only cobalamin replenishment but also immunotherapy. The Japanese Society of Internal Medicine 2022-11-30 2023-07-15 /pmc/articles/PMC10400394/ /pubmed/36450465 http://dx.doi.org/10.2169/internalmedicine.0476-22 Text en Copyright © 2023 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Takeuchi, Yosuke Nomura, Toshiya Nakahara, Keiichi Ueda, Mitsuharu Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance |
title | Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance |
title_full | Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance |
title_fullStr | Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance |
title_full_unstemmed | Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance |
title_short | Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance |
title_sort | autoimmune polyglandular syndrome with refractory gait disturbance |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400394/ https://www.ncbi.nlm.nih.gov/pubmed/36450465 http://dx.doi.org/10.2169/internalmedicine.0476-22 |
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