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Non-traumatic and non-drug-induced rhabdomyolysis

Rhabdomyolysis (RM), a fortunately rare disease of the striated muscle cells, is a complication of non-traumatic (congenital (glycogen storage disease, discrete mitochondrial myopathies and various muscular dystrophies) or acquired (alcoholic myopathy, systemic diseases, arterial occlusion, viral il...

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Autores principales: Kolovou, Genovefa, Cokkinos, Philip, Bilianou, Helen, Kolovou, Vana, Katsiki, Niki, Mavrogeni, Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7191942/
https://www.ncbi.nlm.nih.gov/pubmed/32368681
http://dx.doi.org/10.5114/amsad.2019.90152
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author Kolovou, Genovefa
Cokkinos, Philip
Bilianou, Helen
Kolovou, Vana
Katsiki, Niki
Mavrogeni, Sophie
author_facet Kolovou, Genovefa
Cokkinos, Philip
Bilianou, Helen
Kolovou, Vana
Katsiki, Niki
Mavrogeni, Sophie
author_sort Kolovou, Genovefa
collection PubMed
description Rhabdomyolysis (RM), a fortunately rare disease of the striated muscle cells, is a complication of non-traumatic (congenital (glycogen storage disease, discrete mitochondrial myopathies and various muscular dystrophies) or acquired (alcoholic myopathy, systemic diseases, arterial occlusion, viral illness or bacterial sepsis)) and traumatic conditions. Additionally, RM can occur in some individuals under specific circumstances such as toxic substance use and illicit drug abuse. Lipid-lowering drugs in particular are capable of causing RM. This comprehensive review will focus on non-traumatic and non-drug-induced RM. Moreover, the pathology of RM, its clinical manifestation and biochemical effects, and finally its management will be discussed.
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spelling pubmed-71919422020-05-04 Non-traumatic and non-drug-induced rhabdomyolysis Kolovou, Genovefa Cokkinos, Philip Bilianou, Helen Kolovou, Vana Katsiki, Niki Mavrogeni, Sophie Arch Med Sci Atheroscler Dis State of the Art Paper Rhabdomyolysis (RM), a fortunately rare disease of the striated muscle cells, is a complication of non-traumatic (congenital (glycogen storage disease, discrete mitochondrial myopathies and various muscular dystrophies) or acquired (alcoholic myopathy, systemic diseases, arterial occlusion, viral illness or bacterial sepsis)) and traumatic conditions. Additionally, RM can occur in some individuals under specific circumstances such as toxic substance use and illicit drug abuse. Lipid-lowering drugs in particular are capable of causing RM. This comprehensive review will focus on non-traumatic and non-drug-induced RM. Moreover, the pathology of RM, its clinical manifestation and biochemical effects, and finally its management will be discussed. Termedia Publishing House 2019-12-02 /pmc/articles/PMC7191942/ /pubmed/32368681 http://dx.doi.org/10.5114/amsad.2019.90152 Text en Copyright © 2019 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle State of the Art Paper
Kolovou, Genovefa
Cokkinos, Philip
Bilianou, Helen
Kolovou, Vana
Katsiki, Niki
Mavrogeni, Sophie
Non-traumatic and non-drug-induced rhabdomyolysis
title Non-traumatic and non-drug-induced rhabdomyolysis
title_full Non-traumatic and non-drug-induced rhabdomyolysis
title_fullStr Non-traumatic and non-drug-induced rhabdomyolysis
title_full_unstemmed Non-traumatic and non-drug-induced rhabdomyolysis
title_short Non-traumatic and non-drug-induced rhabdomyolysis
title_sort non-traumatic and non-drug-induced rhabdomyolysis
topic State of the Art Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7191942/
https://www.ncbi.nlm.nih.gov/pubmed/32368681
http://dx.doi.org/10.5114/amsad.2019.90152
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