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Revista Portuguesa de Medicina Geral e Familiar

versión impresa ISSN 2182-5173

Resumen

MOITA, Catarina Ferreira et al. Statin-associated necrotizing myopathy: a rare etiology. Rev Port Med Geral Fam [online]. 2020, vol.36, n.6, pp.503-506.  Epub 01-Dic-2020. ISSN 2182-5173.  https://doi.org/10.32385/rpmgf.v36i6.12629.

Introduction:

Necrotizing autoimmune myopathy is a rare entity characterized by proximal muscle weakness, elevated creatine kinase levels, potential autoantibody presence, and myofiber necrosis with reduced or absent inflammation.

Case description:

We report the case of a 72-year-old female with a 3-week-history of asthenia, increasing proximal tetraparesis, without pain, fever, or other symptoms, and elevated creatine kinase levels. Previous history was remarkable for dyslipidemia controlled with statin therapy. A muscular biopsy was performed, leading to the diagnosis of necrotizing myopathy. A body computed tomography (CT) scan was normal. Corticotherapy was initiated with progressive clinical and analytical improvement.

Discussion:

This case depicts an uncommon and underdiagnosed pathology which may be associated with statin treatment or cancer, that requires an early diagnosis and close follow-up for better clinical outcomes.

Palabras clave : Myositis; Rhabdomyolysis; Hydroxymethylglutaryl-CoA reductase inhibitors; Autoantibodies..

        · resumen en Portugués     · texto en Inglés     · Inglés ( pdf )