gms | German Medical Science

60. Jahrestagung der Deutschen Gesellschaft für Neuropathologie und Neuroanatomie (DGNN)

Deutsche Gesellschaft für Neuropathologie und Neuroanatomie

26. - 28.08.2015, Berlin

Two patients with Statin-induced necrotizing myopathy with similar histology but different clinical behaviour: a diagnostic challenge

Meeting Abstract

  • corresponding author presenting/speaker Clara Frydrychowicz - Universitätsklinikum Leipzig, Neuropathologie, Leipzig, Germany; University, Neuropathology, Leipzig, Germany
  • Lorenz Weidhase - University, ICU, Leipzig, Germany
  • Stefan Merkelbach - Heinrich Braun, Neurology, Zwickau, Germany
  • Wolf Müller - Universitätsklinikum Leipzig, Neuropathologie, Leipzig, Germany

Deutsche Gesellschaft für Neuropathologie und Neuroanatomie. 60th Annual Meeting of the German Society for Neuropathology and Neuroanatomy (DGNN). Berlin, 26.-28.08.2015. Düsseldorf: German Medical Science GMS Publishing House; 2015. Doc15dgnnP41

doi: 10.3205/15dgnn65, urn:nbn:de:0183-15dgnn654

Veröffentlicht: 25. August 2015

© 2015 Frydrychowicz et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

Text

Statins are the most common group of cholesterol lowering medications with more than 100 million prescriptions per year. Statin induced muscular adverse effects occur in 10-25% of patients. We present two cases with Statin- induced necrotizing myopathy. A 70 year old man presented with acute kidney failure due to severe rhabdomyolysis and high creatine kinase (CK) levels. He had a six year history of low dose Statin therapy. Stopping Statin medication led to a fast recovery of muscle related symptoms and CK normalized quickly. A 63 year old woman presented with muscle pain, proximal muscle weakness and mild tetraparesis. She also had been on Statin medication. However, symptoms persisted after Statin had been withdrawn for a period of six months. The two clinical presentations with similar histopathology but different clinical behaviour after Statin- arrest suggest a different pathogenesis. The exact mechanism of Statin-associated myopathies (SAM) still remains elusive. However, a self- limiting Statin induced primarily toxic necrotizing myopathy is now distinguished from a persisting autoimmune mediated Statin- induced necrotizing myopathy. In the latter Anti-HMG- CoA- Reductase- Antibodies can be detected in the serum and muscle of affected patients. Statin-induced autoimmune mediated myopathy was confirmed in the second patient. Neuropathologists should be aware of the possibility of autoimmune mediated Statin- induced necrotizing myopathy and should recommend Anti-HMG-CoA-reductase- Antibody testing in all patients with persistent muscle pathology after Statin-arrest.