Inflammatory myopathy with anti-SRP antibodies: case series of a South Australian cohort

Inflammatory myopathy with anti-SRP antibodies: case series of a South Australian cohort

Myopathy associated with anti-signal recognition particle (SRP) antibodies is a rare form of myopathy, which is thought to be distinct from classic polymyositis. We sought to determine the demographic, clinical and histopathological features of patients with anti-SRP antibodies. Hence we undertook a...

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Bibliographic Details
Published in:Clinical rheumatology Vol. 34; no. 3; pp. 603 - 608
Main Authors: Basnayake, Sajini K, Blumbergs, Peter, Tan, Ju Ann, Roberts-Thompson, Peter J, Limaye, Vidya
Format: Journal Article
Language:English
Published: London Springer London 01-03-2015
Springer Nature B.V
Subjects:
Aged, 80 and over
Case Based Review
Humans
Male
Medicine
Medicine & Public Health
Middle Aged
Muscles - pathology
Myositis - immunology
Myositis - pathology
Rheumatology
Signal Recognition Particle - immunology
Necrotizing myopathy
Myositis
Polymyositis
Histopathology
SRP antibodies
Muscle biopsy
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Summary:Myopathy associated with anti-signal recognition particle (SRP) antibodies is a rare form of myopathy, which is thought to be distinct from classic polymyositis. We sought to determine the demographic, clinical and histopathological features of patients with anti-SRP antibodies. Hence we undertook an audit of patients with histologically-confirmed myositis who had anti-SRP antibodies. Of 144 patients with inflammatory myositis tested for myositis-specific and myositis-associated antibodies between 2007 and 2011 inclusive, five with anti-SRP antibodies were identified. All five were male, four had severe proximal weakness, one was asymptomatic and three had dysphagia. None had cardiovascular involvement. All patients showed isolated anti-SRP positivity and absence of antinuclear antibodies. Muscle histopathology showed variable myofibre necrosis, and most had an inflammatory infiltrate. Majority showed a favorable response to combination immunosuppressive therapy. Myopathy associated with anti-SRP antibodies is clinically heterogeneous in presentation. Muscle histopathology shows a mixture of necrotic and inflammatory features.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
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ISSN:0770-3198
1434-9949
DOI:10.1007/s10067-014-2512-7