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Myasthenia Gravis and Large Granular Lymphocytic Leukemia: a rare association

Myasthenia gravis (MG) is an autoimmune neuromuscular junction disorder sometimes observed in hematologic malignancies as a paraneoplastic syndrome. T-cell Large Granular Lymphocytic Leukemia (T-LGLL) is a rare lymphoproliferative clonal frequently associated with autoimmune disorders. Here we repor...

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Autores principales: Zhang, Yumeng, Varnadoe, Christa, Tandon, Ankita, Forsyth, Peter, Komrokji, Rami, Sokol, Lubomir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568180/
https://www.ncbi.nlm.nih.gov/pubmed/33094093
http://dx.doi.org/10.1016/j.lrr.2020.100226
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author Zhang, Yumeng
Varnadoe, Christa
Tandon, Ankita
Forsyth, Peter
Komrokji, Rami
Sokol, Lubomir
author_facet Zhang, Yumeng
Varnadoe, Christa
Tandon, Ankita
Forsyth, Peter
Komrokji, Rami
Sokol, Lubomir
author_sort Zhang, Yumeng
collection PubMed
description Myasthenia gravis (MG) is an autoimmune neuromuscular junction disorder sometimes observed in hematologic malignancies as a paraneoplastic syndrome. T-cell Large Granular Lymphocytic Leukemia (T-LGLL) is a rare lymphoproliferative clonal frequently associated with autoimmune disorders. Here we report two patients with T-LGLL who developed MG. In both patients the MG was bulbar without generalized weakness and did not involve the thymus. The treatment of T-LGLL led to the resolution of MG symptoms and decrease in acetylcholine receptor antibody titers in both patients suggesting a causative association.
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spelling pubmed-75681802020-10-21 Myasthenia Gravis and Large Granular Lymphocytic Leukemia: a rare association Zhang, Yumeng Varnadoe, Christa Tandon, Ankita Forsyth, Peter Komrokji, Rami Sokol, Lubomir Leuk Res Rep Article Myasthenia gravis (MG) is an autoimmune neuromuscular junction disorder sometimes observed in hematologic malignancies as a paraneoplastic syndrome. T-cell Large Granular Lymphocytic Leukemia (T-LGLL) is a rare lymphoproliferative clonal frequently associated with autoimmune disorders. Here we report two patients with T-LGLL who developed MG. In both patients the MG was bulbar without generalized weakness and did not involve the thymus. The treatment of T-LGLL led to the resolution of MG symptoms and decrease in acetylcholine receptor antibody titers in both patients suggesting a causative association. Elsevier 2020-10-06 /pmc/articles/PMC7568180/ /pubmed/33094093 http://dx.doi.org/10.1016/j.lrr.2020.100226 Text en © 2020 The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Zhang, Yumeng
Varnadoe, Christa
Tandon, Ankita
Forsyth, Peter
Komrokji, Rami
Sokol, Lubomir
Myasthenia Gravis and Large Granular Lymphocytic Leukemia: a rare association
title Myasthenia Gravis and Large Granular Lymphocytic Leukemia: a rare association
title_full Myasthenia Gravis and Large Granular Lymphocytic Leukemia: a rare association
title_fullStr Myasthenia Gravis and Large Granular Lymphocytic Leukemia: a rare association
title_full_unstemmed Myasthenia Gravis and Large Granular Lymphocytic Leukemia: a rare association
title_short Myasthenia Gravis and Large Granular Lymphocytic Leukemia: a rare association
title_sort myasthenia gravis and large granular lymphocytic leukemia: a rare association
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568180/
https://www.ncbi.nlm.nih.gov/pubmed/33094093
http://dx.doi.org/10.1016/j.lrr.2020.100226
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