Myopathy With Anti Signal Recognition Particle Antibody
Journal of the Korean Neurological Association
;
: 231-233, 2011.
Artículo
en Coreano
| WPRIM
| ID: wpr-145202
ABSTRACT
Myopathies associated with anti-signal-recognition particle (SRP) antibodies usually present with severe muscle weakness and exhibit necrotizing myopathy with little inflammation pathologically. Here we report a case of a 61-year-old man who presented with subacute progressive proximal muscle weakness, dysarthria, and dysphagia. Although polymyositis was expected clinically, muscle biopsy revealed myopathic changes with degenerating fibers without definite inflammation. Further laboratory study revealed that the patient was positive for anti-SRP antibodies.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Autoanticuerpos
/
Biopsia
/
Trastornos de Deglución
/
Polimiositis
/
Partícula de Reconocimiento de Señal
/
Debilidad Muscular
/
Disartria
/
Inflamación
/
Anticuerpos
/
Músculos
Límite:
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Neurological Association
Año:
2011
Tipo del documento:
Artículo
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