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An unusual association: anti-Jo1 and anti-SRP antibodies in the serum of a patient with polymyositis

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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.

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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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Written informed consent was obtained from the patient for publication of this case report.

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Correspondence to Katalin Dankó.

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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

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