Internal Medicine · 2017 · 10 citations · 30 references
MedicineImmunologyPathologyImmunopathologyInflammationRheumatologyAutoantibodiesAutoimmune Rheumatic DiseasesAutoimmune VasculitisMuscle PathologyMuscle Strength TestingMusculoskeletal PathologyAnti-neutrophil Cytoplasmic AntibodiesAnti-neutrophil Cytoplasmic Antibody TestingAntineutrophil Cytoplasmic AntibodiesCyclophosphamide-based TherapyFibrinoid NecrosisInflammatory VasculopathyMuscle Biopsy HistologyMuscle Necrosis
A previously healthy 58-year-old man was admitted for muscle pain and weakness [manual muscle testing (MMT) of 4/4 for upper and lower limbs]. We detected elevated levels of inflammatory makers and PR3-anti-neutrophil cytoplasmic antibody (ANCA). Subsequently, the muscle weakness rapidly progressed to an MMT of 2 for all limbs. Magnetic resonance imaging indicated muscle edema, and the creatine kinase (CK) level increased to 29,998 U/L. Methylprednisolone (mPSL) and cyclophosphamide pulse therapy improved the patient symptoms. MMT recovered to 4 for all limbs. A muscle biopsy showed degenerated muscle fibers surrounded by neutrophil-predominant infiltration. In addition, lamina elastic breakdown and fibrinoid necrosis of arterioles were observed. A final diagnosis of microscopic polyangiitis (MPA) limited to the muscles was made.
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