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Multiple myeloma presenting as an intramedullary spinal cord tumor: a case report and review of the literature

BACKGROUND: Extramedullary disease in multiple myeloma often portends a worse diagnosis. In approximately 1% of cases, multiple myeloma may metastasize to the central nervous system as either leptomeningeal involvement or an intracranial, intraparenchymal lesion. Spinal cord metastases, however, are...

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Autores principales: Di, Long, Huang, Kevin, Kesayan, Tigran, Kroll, Derek, Baz, Rachid C., Macaulay, Robert J., Tran, Nam D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566029/
https://www.ncbi.nlm.nih.gov/pubmed/33059729
http://dx.doi.org/10.1186/s13256-020-02496-5
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author Di, Long
Huang, Kevin
Kesayan, Tigran
Kroll, Derek
Baz, Rachid C.
Macaulay, Robert J.
Tran, Nam D.
author_facet Di, Long
Huang, Kevin
Kesayan, Tigran
Kroll, Derek
Baz, Rachid C.
Macaulay, Robert J.
Tran, Nam D.
author_sort Di, Long
collection PubMed
description BACKGROUND: Extramedullary disease in multiple myeloma often portends a worse diagnosis. In approximately 1% of cases, multiple myeloma may metastasize to the central nervous system as either leptomeningeal involvement or an intracranial, intraparenchymal lesion. Spinal cord metastases, however, are exceedingly rare. We present a case of spinal cord multiple myeloma as well as a literature review of reported cases. CASE PRESENTATION: A 66-year-old African American man with multiple myeloma presented with acute midthoracic pain and lower extremity paresis and paresthesia. Magnetic resonance imaging of the spine revealed two contrast-enhancing intramedullary enhancing lesions in the T1–T2 and T6–T7 cord. Resection with biopsy yielded a diagnosis of metastatic multiple myeloma. CONCLUSION: To date, only six cases of extramedullary disease to the spinal cord in patients with multiple myeloma have been reported, including our patient’s case. In all cases, neurologic deficit was observed at presentation, and magnetic resonance imaging of the spine revealed an intramedullary, homogeneously enhancing lesion. Current evidence suggests worse prognosis in patients with extramedullary disease to the central nervous system, and treatment paradigms remain debatable.
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spelling pubmed-75660292020-10-20 Multiple myeloma presenting as an intramedullary spinal cord tumor: a case report and review of the literature Di, Long Huang, Kevin Kesayan, Tigran Kroll, Derek Baz, Rachid C. Macaulay, Robert J. Tran, Nam D. J Med Case Rep Case Report BACKGROUND: Extramedullary disease in multiple myeloma often portends a worse diagnosis. In approximately 1% of cases, multiple myeloma may metastasize to the central nervous system as either leptomeningeal involvement or an intracranial, intraparenchymal lesion. Spinal cord metastases, however, are exceedingly rare. We present a case of spinal cord multiple myeloma as well as a literature review of reported cases. CASE PRESENTATION: A 66-year-old African American man with multiple myeloma presented with acute midthoracic pain and lower extremity paresis and paresthesia. Magnetic resonance imaging of the spine revealed two contrast-enhancing intramedullary enhancing lesions in the T1–T2 and T6–T7 cord. Resection with biopsy yielded a diagnosis of metastatic multiple myeloma. CONCLUSION: To date, only six cases of extramedullary disease to the spinal cord in patients with multiple myeloma have been reported, including our patient’s case. In all cases, neurologic deficit was observed at presentation, and magnetic resonance imaging of the spine revealed an intramedullary, homogeneously enhancing lesion. Current evidence suggests worse prognosis in patients with extramedullary disease to the central nervous system, and treatment paradigms remain debatable. BioMed Central 2020-10-16 /pmc/articles/PMC7566029/ /pubmed/33059729 http://dx.doi.org/10.1186/s13256-020-02496-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Di, Long
Huang, Kevin
Kesayan, Tigran
Kroll, Derek
Baz, Rachid C.
Macaulay, Robert J.
Tran, Nam D.
Multiple myeloma presenting as an intramedullary spinal cord tumor: a case report and review of the literature
title Multiple myeloma presenting as an intramedullary spinal cord tumor: a case report and review of the literature
title_full Multiple myeloma presenting as an intramedullary spinal cord tumor: a case report and review of the literature
title_fullStr Multiple myeloma presenting as an intramedullary spinal cord tumor: a case report and review of the literature
title_full_unstemmed Multiple myeloma presenting as an intramedullary spinal cord tumor: a case report and review of the literature
title_short Multiple myeloma presenting as an intramedullary spinal cord tumor: a case report and review of the literature
title_sort multiple myeloma presenting as an intramedullary spinal cord tumor: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566029/
https://www.ncbi.nlm.nih.gov/pubmed/33059729
http://dx.doi.org/10.1186/s13256-020-02496-5
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