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Pathological findings with vacuoles in anti-mitochondrial antibody-positive inflammatory myopathy
Yuanchong Chen1,2, Wei Zhang1, He Lv1
1Department of Neurology, Peking University First Hospital, No.8 Xishiku Street, Xicheng District, Beijing, 100034, China.
Background:
A few patients with inflammatory myopathy showed anti-mitochondrial antibody (AMA) positivity. This study aimed to report the clinical and pathological findings with vacuoles in 3 cases of such patients.
Methods:
Three cases with myositis from the Myositis Clinical Database of Peking University First Hospital were identified with AMA positivity. Their clinical records were retrospectively reviewed and the data was extracted. All the 3 cases underwent muscle biopsy.
Results:
Three middle-aged patients presented with chronic-onset weakness of proximal limbs, marked elevation of creatine kinase, and AMA-positivity. Two of the 3 cases meet the criteria of primary biliary cholangitis. All the 3 cases presented with cardiac involvement and proteinuria. Two cases developed type 2 respiratory failure. MRI of the thigh muscle showed multiple patches of edema bilaterally in both cases, mostly in the adductor magnus. Pathological findings include degeneration of muscle fibers, diffused MHC-I positivity, and complement deposits on cell membranes. Vacuoles without rims of different sizes were discovered under the membrane of the muscle fibers. A few RBFs were discovered in case 1, while a diffused proliferation of endomysium and perimysium was shown in case 2.
Conclusions:
AMA-positive inflammatory myopathy is a disease that could affect multiple systems. Apart from inflammatory changes, the pathological findings of muscle can also present vacuoles.
Insights
Anti-mitochondrial antibody (AMA)-positive inflammatory myopathy presents with systemic involvement and characteristic muscle vacuoles. This study details the clinical and pathological findings in three such cases.
Area of Science:
- Rheumatology
- Neurology
- Immunology
Background:
- Inflammatory myopathy can present with anti-mitochondrial antibody (AMA) positivity in a subset of patients.
- This study focuses on three cases of AMA-positive inflammatory myopathy.
Purpose of the Study:
- To report the clinical and pathological findings in patients with inflammatory myopathy and anti-mitochondrial antibody (AMA) positivity.
- To investigate the presence of vacuoles in muscle biopsies of these patients.
Main Methods:
- Retrospective review of clinical records from three AMA-positive myositis patients.
- Analysis of muscle biopsy findings, including histopathology and immunohistochemistry.
Main Results:
- Three middle-aged patients exhibited chronic proximal limb weakness, elevated creatine kinase, and AMA positivity.
- Two patients met criteria for primary biliary cholangitis; all had cardiac involvement and proteinuria.
- Muscle pathology revealed fiber degeneration, MHC-I positivity, complement deposition, and unique vacuoles.
Conclusions:
- AMA-positive inflammatory myopathy is a multisystem disease.
- Muscle biopsy findings in these patients can include vacuoles, in addition to inflammatory changes.
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