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Updated: Jul 17, 2026

Noninvasive Assessment of Cardiac Abnormalities in Experimental Autoimmune Myocarditis by Magnetic Resonance Microscopy Imaging in the Mouse
Published on: June 20, 2014
[A case of chronic multifocal myositis]
T Maruyama1, K Kondo, K Tabata
1Department of Neurology, Kakeyu Rehabilitation Center.
This study details a rare case of asymmetrical muscle atrophy with preserved strength, presenting unique diagnostic challenges. Findings suggest a complex myopathy requiring further investigation for effective treatment.
Area of Science:
- Neurology
- Muscle Physiology
- Pathology
Background:
- Presents a unique case of a 61-year-old male with slowly progressive, asymmetrical muscle atrophy.
- Symptoms began at age 56, initially affecting the right shoulder and left arm, later progressing to thighs.
Observation:
- Notable muscle wasting in the trapezius, proximal upper and lower extremities, with asymmetry.
- Muscle strength was relatively preserved despite significant atrophy.
- Elevated creatine kinase and myoglobin levels, with normal nerve conduction studies.
Findings:
- Electromyography revealed combined myopathic and neuropathic changes.
- Computed tomography (CT) showed asymmetrical muscle atrophy and patchy low-density areas.
- Muscle biopsy demonstrated fiber size variation, necrosis, regeneration, central nuclei, fibrosis, and mononuclear inflammatory infiltration.
Implications:
- Highlights the diagnostic complexity of asymmetrical myopathies.
- Suggests a potential inflammatory or degenerative process affecting skeletal muscles.
- Underscores the importance of integrated diagnostic approaches including imaging and biopsy for rare muscle disorders.
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