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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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Detalles Bibliográficos
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
Descripción
Sumario: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.