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Differential Diagnoses of Inclusion Body Myositis

Vivekanandam, V; Bugiardini, E; Merve, A; Parton, M; Morrow, JM; Hanna, MG; Machado, PM; (2020) Differential Diagnoses of Inclusion Body Myositis. Neurologic Clinics , 38 (3) pp. 697-710. 10.1016/j.ncl.2020.03.014. Green open access

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Abstract

Inclusion body myositis is a slowly progressive myopathy, characteristically affecting quadriceps and long finger flexors. Atypical presentations do occur, however, and there is overlap with other myopathies, including inflammatory and hereditary etiologies. This article discusses atypical cases and differential diagnoses and considers the role of imaging and histopathology in differentiating inclusion body myositis.

Type: Article
Title: Differential Diagnoses of Inclusion Body Myositis
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1016/j.ncl.2020.03.014
Publisher version: https://doi.org/10.1016/j.ncl.2020.03.014
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher's terms and conditions.
Keywords: Diagnosis, Inclusion body myositis, Inflammatory myopathy, Magnetic resonance imaging, Muscle biopsy, Muscular dystrophy
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
URI: https://discovery.ucl.ac.uk/id/eprint/10110268
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