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Case report: Persistent hypogammaglobulinemia in thymoma-associated myasthenia gravis: the impact of rituximab or Good's syndrome?
INTRODUCTION: Rituximab (RTX) showed good efficacy and safety for patients with myasthenia gravis. However, the percentage of peripheral CD20+ B cell may be absent for years after low dose of RTX treatment. Persistent hypogammaglobulinemia and opportunistic infection may occur in patients under trea...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196171/ https://www.ncbi.nlm.nih.gov/pubmed/37213908 http://dx.doi.org/10.3389/fneur.2023.1152992 |
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author | Ren, Jingru Wang, Jianchun Liu, Ran Guo, Jing Yao, Yan Luo, Jingjing Hao, Hongjun Gao, Feng |
author_facet | Ren, Jingru Wang, Jianchun Liu, Ran Guo, Jing Yao, Yan Luo, Jingjing Hao, Hongjun Gao, Feng |
author_sort | Ren, Jingru |
collection | PubMed |
description | INTRODUCTION: Rituximab (RTX) showed good efficacy and safety for patients with myasthenia gravis. However, the percentage of peripheral CD20+ B cell may be absent for years after low dose of RTX treatment. Persistent hypogammaglobulinemia and opportunistic infection may occur in patients under treatment of RTX with thymoma relapse. CASE REPRESENTATION: We report a case of refractory myasthenia gravis. After two doses of 100 mg rituximab, the patient developed transient neutropenia. The peripheral blood CD20+ B cell percentage was 0 more than 3 years. Eighteen months later, the patient's symptoms relapsed with thymoma recurred. She had persistent hypogammaglobulinemia and multiple opportunistic infections. CONCLUSION: In MG patient under B cell depletion therapy had thymoma relapse, Good's syndrome may induce prolonged B cell depletion, hypogammaglobulinemia and opportunistic infections. |
format | Online Article Text |
id | pubmed-10196171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101961712023-05-20 Case report: Persistent hypogammaglobulinemia in thymoma-associated myasthenia gravis: the impact of rituximab or Good's syndrome? Ren, Jingru Wang, Jianchun Liu, Ran Guo, Jing Yao, Yan Luo, Jingjing Hao, Hongjun Gao, Feng Front Neurol Neurology INTRODUCTION: Rituximab (RTX) showed good efficacy and safety for patients with myasthenia gravis. However, the percentage of peripheral CD20+ B cell may be absent for years after low dose of RTX treatment. Persistent hypogammaglobulinemia and opportunistic infection may occur in patients under treatment of RTX with thymoma relapse. CASE REPRESENTATION: We report a case of refractory myasthenia gravis. After two doses of 100 mg rituximab, the patient developed transient neutropenia. The peripheral blood CD20+ B cell percentage was 0 more than 3 years. Eighteen months later, the patient's symptoms relapsed with thymoma recurred. She had persistent hypogammaglobulinemia and multiple opportunistic infections. CONCLUSION: In MG patient under B cell depletion therapy had thymoma relapse, Good's syndrome may induce prolonged B cell depletion, hypogammaglobulinemia and opportunistic infections. Frontiers Media S.A. 2023-05-05 /pmc/articles/PMC10196171/ /pubmed/37213908 http://dx.doi.org/10.3389/fneur.2023.1152992 Text en Copyright © 2023 Ren, Wang, Liu, Guo, Yao, Luo, Hao and Gao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Ren, Jingru Wang, Jianchun Liu, Ran Guo, Jing Yao, Yan Luo, Jingjing Hao, Hongjun Gao, Feng Case report: Persistent hypogammaglobulinemia in thymoma-associated myasthenia gravis: the impact of rituximab or Good's syndrome? |
title | Case report: Persistent hypogammaglobulinemia in thymoma-associated myasthenia gravis: the impact of rituximab or Good's syndrome? |
title_full | Case report: Persistent hypogammaglobulinemia in thymoma-associated myasthenia gravis: the impact of rituximab or Good's syndrome? |
title_fullStr | Case report: Persistent hypogammaglobulinemia in thymoma-associated myasthenia gravis: the impact of rituximab or Good's syndrome? |
title_full_unstemmed | Case report: Persistent hypogammaglobulinemia in thymoma-associated myasthenia gravis: the impact of rituximab or Good's syndrome? |
title_short | Case report: Persistent hypogammaglobulinemia in thymoma-associated myasthenia gravis: the impact of rituximab or Good's syndrome? |
title_sort | case report: persistent hypogammaglobulinemia in thymoma-associated myasthenia gravis: the impact of rituximab or good's syndrome? |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196171/ https://www.ncbi.nlm.nih.gov/pubmed/37213908 http://dx.doi.org/10.3389/fneur.2023.1152992 |
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