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Cancer-associated myositis: an elusive entity

Inflammatory myopathies are characterized by the skeletal muscle inflammation leading to symptoms of myopathy along with varying involvement of other organs such as lung, skin and joints. The strong association between inflammatory myopathies and malignancy has been well recognized. Recently, ‘can...

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Detalles Bibliográficos
Autores principales: Fayyaz, Beenish, Rehman, Hafiz J., Uqdah, Hakim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374925/
https://www.ncbi.nlm.nih.gov/pubmed/30788076
http://dx.doi.org/10.1080/20009666.2019.1571880
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author Fayyaz, Beenish
Rehman, Hafiz J.
Uqdah, Hakim
author_facet Fayyaz, Beenish
Rehman, Hafiz J.
Uqdah, Hakim
author_sort Fayyaz, Beenish
collection PubMed
description Inflammatory myopathies are characterized by the skeletal muscle inflammation leading to symptoms of myopathy along with varying involvement of other organs such as lung, skin and joints. The strong association between inflammatory myopathies and malignancy has been well recognized. Recently, ‘cancer-associated myositis (CAM)’, has been proposed to be a paraneoplastic syndrome due to the anti-tumor immunity secondary to similar tumor and regenerating muscle antigens. As the prognosis of myositis depends on the prognosis and treatment of the underlying malignancy, physicians must determine the degree of testing necessary to detect cancer both at myositis onset and thereafter. However, there are no clear guidelines regarding the best approach. Emerging medical evidence shows that identification of certain risk factors and serology patterns can be utilized to predict cancer risk in patients with myositis.
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spelling pubmed-63749252019-02-20 Cancer-associated myositis: an elusive entity Fayyaz, Beenish Rehman, Hafiz J. Uqdah, Hakim J Community Hosp Intern Med Perspect Case Report Inflammatory myopathies are characterized by the skeletal muscle inflammation leading to symptoms of myopathy along with varying involvement of other organs such as lung, skin and joints. The strong association between inflammatory myopathies and malignancy has been well recognized. Recently, ‘cancer-associated myositis (CAM)’, has been proposed to be a paraneoplastic syndrome due to the anti-tumor immunity secondary to similar tumor and regenerating muscle antigens. As the prognosis of myositis depends on the prognosis and treatment of the underlying malignancy, physicians must determine the degree of testing necessary to detect cancer both at myositis onset and thereafter. However, there are no clear guidelines regarding the best approach. Emerging medical evidence shows that identification of certain risk factors and serology patterns can be utilized to predict cancer risk in patients with myositis. Taylor & Francis 2019-02-11 /pmc/articles/PMC6374925/ /pubmed/30788076 http://dx.doi.org/10.1080/20009666.2019.1571880 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Fayyaz, Beenish
Rehman, Hafiz J.
Uqdah, Hakim
Cancer-associated myositis: an elusive entity
title Cancer-associated myositis: an elusive entity
title_full Cancer-associated myositis: an elusive entity
title_fullStr Cancer-associated myositis: an elusive entity
title_full_unstemmed Cancer-associated myositis: an elusive entity
title_short Cancer-associated myositis: an elusive entity
title_sort cancer-associated myositis: an elusive entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374925/
https://www.ncbi.nlm.nih.gov/pubmed/30788076
http://dx.doi.org/10.1080/20009666.2019.1571880
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