Thrombotic microangiopathy observed in the course of SRP autoimmune necrotising myopathy

A Japanese team of neurologists and nephrologists report the observation of a 61-year-old patient diagnosed with autoimmune necrotising myopathy:

  • the clinical history and the positivity of anti-SRP autoantibodies were consistent with this diagnosis,
  • treatment consisted of corticosteroids and immunoglobulins, followed by tacrolimus,
  • eight weeks after initiation of this treatment, thrombotic microangiopathy was observed and confirmed by renal biopsy, necessitating haemodialysis.

The authors point to the responsibility of anti-SRP autoantibodies rather than iatrogenesis.

 

Thrombotic microangiopathy in a patient with anti-signal recognition particle antibody-positive immune-mediated necrotizing myopathy. Sakai K, Takahashi M, Ito Y et al. Int J Rheum Dis. 2023 Oct 12