Anti-Signal Recognition Particle Myopathy in a Geriatric Patient


Autoria(s): Ferreira, Diana Marques; Afonso Mendes, Patrícia; Aragão, António; Veríssimo, Manuel Teixeira; Carvalho, Armando
Data(s)

2015

Resumo

Anti-signal recognition particle (SRP) myopathy is a rare idiopathic inflammatory myositis that usually affects middle-age women, and is characterized by rapidly progressive proximal and symmetrical muscle weakness, elevated creatine kinase levels, severe necrotizing immune-mediated myopathy, presence of anti-SRP autoantibodies and poor response to steroid therapy. We report a geriatric case of a previously independent patient, presenting with slow onset of proximal paraparesis, myalgia and severe gait impairment. The patient was treated with steroid and azathioprine, with laboratory and pain response but modest muscle strength improvement. The clinical presentation of this unusual patient was atypical, which hampered the correct diagnosis.

Formato

text

Identificador

http://eprints.bice.rm.cnr.it/15086/1/311-2249-1-PB.pdf

Ferreira, Diana Marques and Afonso Mendes, Patrícia and Aragão, António and Veríssimo, Manuel Teixeira and Carvalho, Armando (2015) Anti-Signal Recognition Particle Myopathy in a Geriatric Patient. European Journal of Case Reports in Internal Medicine, 2 (7). pp. 1-3. ISSN 2284-2594

Idioma(s)

en

Publicador

SMC media

Relação

http://eprints.bice.rm.cnr.it/15086/

http://www.ejcrim.com/index.php/EJCRIM/article/view/311

10.12890/2015_000311

Palavras-Chave #616 Malattie (classificare qui la Clinica medica, la medicina basata sull'evidenza, la Medicina interna, la Medicina sperimentale)
Tipo

Article

PeerReviewed