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30 November 2016

2 Pages

Rhabdomyolysis and Autoimmune Variant Stiff-Person Syndrome

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1
Division of Vascular Neurology, Department of Neurology, University of South Florida, Morsani College of Medicine, 12901 Bruce B Downs Blvd, MDC 55, Tampa, FL 33612, USA
2
Department of Neurology, James A Haley Veterans Hospital, Tampa, FL 33612, USA
*
Author to whom correspondence should be addressed.

Abstract

Stiff-person syndrome (SPS) is a rare neurologic disorder characterized by waxing and waning muscular rigidity, stiffness and spasms. Three subtypes have been described: paraneoplastic, autoimmune and idiopathic. Rhabdomyolysis has been described in the paraneoplastic variant, but to our knowledge no case has been reported involving the autoimmune variant. We report a case report of a 50-year-old man with history of SPS who presented with recurrent episodes of severe limb and back spasms. He was hospitalized on two separate occasions for uncontrollable spasms associated with renal failure and creatinine phosphokinase elevations of 55,000 and 22,000 U/L respectively. Laboratory tests were otherwise unremarkable. The acute renal failure resolved during both admissions with supportive management. Rhabdomyolysis has the potential to be fatal and early diagnosis is essential. It should be considered in patients who have SPS and are experiencing an exacerbation of their neurologic condition.

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