Myositis with antimitochondrial antibodies diagnosed by rectus abdominis muscle biopsy
| Autor: | Takeshi Uenaka, Fumio Kanda, Hisatomo Kowa, Yoshihisa Ohtsuka, Kakuya Nagata, Tatsushi Toda, Kenji Sekiguchi |
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| Rok vydání: | 2013 |
| Předmět: |
Pathology
medicine.medical_specialty Muscle biopsy medicine.diagnostic_test Physiology business.industry Autoantibody medicine.disease Polymyositis Biceps Cellular and Molecular Neuroscience Primary biliary cirrhosis Physiology (medical) Biopsy medicine Neurology (clinical) skin and connective tissue diseases business Rectus abdominis muscle Myositis |
| Zdroj: | Muscle & Nerve. 47:766-768 |
| ISSN: | 0148-639X |
| Popis: | Introduction Antimitochondrial antibodies are autoantibodies detected in 90% of primary biliary cirrhosis (PBC) patients. Some PBC cases are complicated by myositis, which is difficult to confirm due to minimal histological evidence of inflammation in limb muscles. Methods Our aim was to determine the extent of inflammatory changes in a truncal muscle biopsy specimen from a PBC patient. Results A 48-year-old woman with a 5-year history of atrial fibrillation and chronic heart failure was evaluated for elevated serum creatine kinase level. Antimitochondrial M2 antibodies were detected, and PBC was diagnosed. A biceps brachii biopsy specimen showed mild, non-specific myogenic changes; a second biopsy was performed on the rectus abdominis muscle, which showed typical inflammatory changes. Myositis with antimitochondrial M2 antibodies was confirmed. Conclusions In myositis patients with antimitochondrial M2 antibodies, muscles of the extremities are involved to a lesser extent. Radiological and histological examination focusing on truncal muscles, including a biopsy, is important. Muscle Nerve 47: 766–768, 2013 |
| Databáze: | OpenAIRE |
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