Metabolic myopathy presenting with polyarteritis nodosa: a case report

<p>Abstract</p> <p>Introduction</p> <p>To the best of our knowledge, we describe for the first time a patient in whom an unusual metabolic myopathy was identified after failure to respond to curative therapy for a systemic vasculitis, polyarteritis nodosa. We hope this...

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Main Authors: Elbalkhi Amro, Abdullah Mishal, Vishwanath Sahana, Ambrus Julian L
Format: Article
Language:English
Published: BMC 2011-06-01
Series:Journal of Medical Case Reports
Online Access:http://www.jmedicalcasereports.com/content/5/1/262
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spelling doaj-6f148c4d90ad40aab2e8573f8943c6112020-11-25T00:26:06ZengBMCJournal of Medical Case Reports1752-19472011-06-015126210.1186/1752-1947-5-262Metabolic myopathy presenting with polyarteritis nodosa: a case reportElbalkhi AmroAbdullah MishalVishwanath SahanaAmbrus Julian L<p>Abstract</p> <p>Introduction</p> <p>To the best of our knowledge, we describe for the first time a patient in whom an unusual metabolic myopathy was identified after failure to respond to curative therapy for a systemic vasculitis, polyarteritis nodosa. We hope this report will heighten awareness of common metabolic myopathies that may present later in life. It also speculates on the potential relationship between metabolic myopathy and systemic vasculitis.</p> <p>Case presentation</p> <p>A 78-year-old African-American woman with a two-year history of progressive fatigue and exercise intolerance presented to our facility with new skin lesions and profound muscle weakness. Skin and muscle biopsies demonstrated a medium-sized artery vasculitis consistent with polyarteritis nodosa. Biochemical studies of the muscle revealed diminished cytochrome C oxidase activity (0.78 μmol/minute/g tissue; normal range 1.03 to 3.83 μmol/minute/g tissue), elevated acid maltase activity (23.39 μmol/minute/g tissue; normal range 1.74 to 9.98 μmol/minute/g tissue) and elevated neutral maltase activity (35.89 μmol/minute/g tissue; normal range 4.35 to 16.03 μmol/minute/g tissue). Treatment for polyarteritis nodosa with prednisone and cyclophosphamide resulted in minimal symptomatic improvement. Additional management with a diet low in complex carbohydrates and ubiquinone, creatine, carnitine, folic acid, α-lipoic acid and ribose resulted in dramatic clinical improvement.</p> <p>Conclusions</p> <p>Our patient's initial symptoms of fatigue, exercise intolerance and progressive weakness were likely related to her complex metabolic myopathy involving both the mitochondrial respiratory chain and glycogen storage pathways. Management of our patient required treatment of both the polyarteritis nodosa as well as metabolic myopathy. Metabolic myopathies are common and should be considered in any patient with exercise intolerance. Metabolic myopathies may complicate the management of various disease states.</p> http://www.jmedicalcasereports.com/content/5/1/262
collection DOAJ
language English
format Article
sources DOAJ
author Elbalkhi Amro
Abdullah Mishal
Vishwanath Sahana
Ambrus Julian L
spellingShingle Elbalkhi Amro
Abdullah Mishal
Vishwanath Sahana
Ambrus Julian L
Metabolic myopathy presenting with polyarteritis nodosa: a case report
Journal of Medical Case Reports
author_facet Elbalkhi Amro
Abdullah Mishal
Vishwanath Sahana
Ambrus Julian L
author_sort Elbalkhi Amro
title Metabolic myopathy presenting with polyarteritis nodosa: a case report
title_short Metabolic myopathy presenting with polyarteritis nodosa: a case report
title_full Metabolic myopathy presenting with polyarteritis nodosa: a case report
title_fullStr Metabolic myopathy presenting with polyarteritis nodosa: a case report
title_full_unstemmed Metabolic myopathy presenting with polyarteritis nodosa: a case report
title_sort metabolic myopathy presenting with polyarteritis nodosa: a case report
publisher BMC
series Journal of Medical Case Reports
issn 1752-1947
publishDate 2011-06-01
description <p>Abstract</p> <p>Introduction</p> <p>To the best of our knowledge, we describe for the first time a patient in whom an unusual metabolic myopathy was identified after failure to respond to curative therapy for a systemic vasculitis, polyarteritis nodosa. We hope this report will heighten awareness of common metabolic myopathies that may present later in life. It also speculates on the potential relationship between metabolic myopathy and systemic vasculitis.</p> <p>Case presentation</p> <p>A 78-year-old African-American woman with a two-year history of progressive fatigue and exercise intolerance presented to our facility with new skin lesions and profound muscle weakness. Skin and muscle biopsies demonstrated a medium-sized artery vasculitis consistent with polyarteritis nodosa. Biochemical studies of the muscle revealed diminished cytochrome C oxidase activity (0.78 μmol/minute/g tissue; normal range 1.03 to 3.83 μmol/minute/g tissue), elevated acid maltase activity (23.39 μmol/minute/g tissue; normal range 1.74 to 9.98 μmol/minute/g tissue) and elevated neutral maltase activity (35.89 μmol/minute/g tissue; normal range 4.35 to 16.03 μmol/minute/g tissue). Treatment for polyarteritis nodosa with prednisone and cyclophosphamide resulted in minimal symptomatic improvement. Additional management with a diet low in complex carbohydrates and ubiquinone, creatine, carnitine, folic acid, α-lipoic acid and ribose resulted in dramatic clinical improvement.</p> <p>Conclusions</p> <p>Our patient's initial symptoms of fatigue, exercise intolerance and progressive weakness were likely related to her complex metabolic myopathy involving both the mitochondrial respiratory chain and glycogen storage pathways. Management of our patient required treatment of both the polyarteritis nodosa as well as metabolic myopathy. Metabolic myopathies are common and should be considered in any patient with exercise intolerance. Metabolic myopathies may complicate the management of various disease states.</p>
url http://www.jmedicalcasereports.com/content/5/1/262
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