Abstract
The idiopathic inflammatory myopathies are systemic autoimmune diseases characterized by chronic inflammation, resulting in the progressive weakness of the proximal muscles. Myositis-specific or myositis-associated autoantibodies can often be found in serum of polymyositis and dermatomyositis patients. This autoantibody presence may play a significant role in patient diagnosis and classification. We present a female polymyositis patient characterized with serious muscle weakness and lung involvement. Anti-Jo1 antibodies were detected in the patient’s serum at the time of diagnosis. After 5 years of treatment and surveillance, recent laboratory analysis showed the presence anti-SRP antibody in her serum.
Abbreviations
- IIM:
-
Idiopathic inflammatory myopathies
- PM:
-
Polymyositis
- MSA:
-
Myositis-specific autoantibodies
- MAA:
-
Myositis-associated autoantibodies
- CK:
-
Serum creatine kinase
- LDH:
-
Serum lactate dehydrogenase
- SGOT:
-
Serum aspartate aminotransferase
- SGPT:
-
Serum alanine aminotransferase
- Anti-Jo-1:
-
Anti-histidyl-tRNA antibody
- Anti-SRP:
-
Antibody against signal recognition particle
- EMG:
-
Electromyography
- ENG:
-
Electroneurography
- HRCT:
-
High resolution computer tomography
- ILD:
-
Intersticial lung disease
- Qol:
-
Quality of life
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Vincze, M., Molnár, P.A., Tumpek, J. et al. An unusual association: anti-Jo1 and anti-SRP antibodies in the serum of a patient with polymyositis. Clin Rheumatol 29, 811–814 (2010). https://doi.org/10.1007/s10067-010-1394-6
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DOI: https://doi.org/10.1007/s10067-010-1394-6