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Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report
BACKGROUND: Bortezomib is a first-line drug approved for patients with multiple myeloma (MM) and has significantly increased their overall survival. However, bortezomib-induced peripheral neuropathy (PN) remains a significant side effect that has led to its discontinuation in some patients. Guillain...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789385/ https://www.ncbi.nlm.nih.gov/pubmed/31616710 http://dx.doi.org/10.12998/wjcc.v7.i18.2905 |
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author | Xu, Yu-Ling Zhao, Wei-Hua Tang, Zhong-Yuan Li, Zhong-Qing Long, Yuan Cheng, Peng Luo, Jun |
author_facet | Xu, Yu-Ling Zhao, Wei-Hua Tang, Zhong-Yuan Li, Zhong-Qing Long, Yuan Cheng, Peng Luo, Jun |
author_sort | Xu, Yu-Ling |
collection | PubMed |
description | BACKGROUND: Bortezomib is a first-line drug approved for patients with multiple myeloma (MM) and has significantly increased their overall survival. However, bortezomib-induced peripheral neuropathy (PN) remains a significant side effect that has led to its discontinuation in some patients. Guillain-Barré syndrome (GBS) is recognized as an immune-mediated PN characterized by the involvement of multiple nerve roots and peripheral nerves and albuminocytologic dissociation in cerebrospinal fluid (CSF) tests. Intravenous immunoglobulin (IVIG) and plasmapheresis are effective. CASE SUMMARY: A 45-year-old man diagnosed with stage III MM (λ type) was treated with bortezomib and dexamethasone. Fourteen days after the second course, he complained of intense burning sensation in the lower limbs and hands, loss of tactile sensation, and pain in the distal area of both thighs and in the distal part of both wrist joints. Neurological examination revealed absence of knee and ankle reflexes. CSF examination revealed albuminocytologic dissociation. Nerve conduction studies indicated sensory nerve action potential amplitudes, conduction velocity decrease, and F wave latency prolongation. He was diagnosed as MM complicated with GBS. Subsequently, he was treated with high-dose IVIG (400 mg/kg/d for five days). His symptoms fully resolved without relapse at the 6-month follow-up. CONCLUSION: Our case highlights the differential diagnosis and management of complications after bortezomib treatment in MM. |
format | Online Article Text |
id | pubmed-6789385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-67893852019-10-15 Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report Xu, Yu-Ling Zhao, Wei-Hua Tang, Zhong-Yuan Li, Zhong-Qing Long, Yuan Cheng, Peng Luo, Jun World J Clin Cases Case Report BACKGROUND: Bortezomib is a first-line drug approved for patients with multiple myeloma (MM) and has significantly increased their overall survival. However, bortezomib-induced peripheral neuropathy (PN) remains a significant side effect that has led to its discontinuation in some patients. Guillain-Barré syndrome (GBS) is recognized as an immune-mediated PN characterized by the involvement of multiple nerve roots and peripheral nerves and albuminocytologic dissociation in cerebrospinal fluid (CSF) tests. Intravenous immunoglobulin (IVIG) and plasmapheresis are effective. CASE SUMMARY: A 45-year-old man diagnosed with stage III MM (λ type) was treated with bortezomib and dexamethasone. Fourteen days after the second course, he complained of intense burning sensation in the lower limbs and hands, loss of tactile sensation, and pain in the distal area of both thighs and in the distal part of both wrist joints. Neurological examination revealed absence of knee and ankle reflexes. CSF examination revealed albuminocytologic dissociation. Nerve conduction studies indicated sensory nerve action potential amplitudes, conduction velocity decrease, and F wave latency prolongation. He was diagnosed as MM complicated with GBS. Subsequently, he was treated with high-dose IVIG (400 mg/kg/d for five days). His symptoms fully resolved without relapse at the 6-month follow-up. CONCLUSION: Our case highlights the differential diagnosis and management of complications after bortezomib treatment in MM. Baishideng Publishing Group Inc 2019-09-26 2019-09-26 /pmc/articles/PMC6789385/ /pubmed/31616710 http://dx.doi.org/10.12998/wjcc.v7.i18.2905 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Xu, Yu-Ling Zhao, Wei-Hua Tang, Zhong-Yuan Li, Zhong-Qing Long, Yuan Cheng, Peng Luo, Jun Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report |
title | Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report |
title_full | Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report |
title_fullStr | Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report |
title_full_unstemmed | Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report |
title_short | Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report |
title_sort | guillain-barré syndrome in a patient with multiple myeloma after bortezomib therapy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789385/ https://www.ncbi.nlm.nih.gov/pubmed/31616710 http://dx.doi.org/10.12998/wjcc.v7.i18.2905 |
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