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Korean Journal of Neuromuscular Disorders 2016;8(1):22-27.
Rhabdomyolysis
Jung Hwan Lee, Young-Chul Choi
Department of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea
횡문근융해증의 이해
이정환, 최영철
연세대학교 의과대학 강남세브란스병원 신경과
Abstract
Rhabdomyolysis is commonly defined as elevation of serum creatine kinase (sCK) level of above 10 times the upper limit of normal followed by a rapid decrease to normal values. Typical clinical features are myalgia, muscular weakness and black colored urine and the most common complication is acute renal failure due to acute tubular necrosis as a result of mechanical obstruction by myoglobin. Most patients experience one episode of rhabdomyolysis by substance abuse, medication, trauma, or seizures. When patients have a history of recurrent rhabdomyolysis, exercise intolerance or family members with neuromuscular disorders, further evaluations for genetic neuromuscular disorder are required. Mortality rate of rhabdomyolysis is, generally, below 10%, but very high in patients with acute renal failure. So, the management in the acute phase should be performed with maintenance of renal function and restore of metabolic derangements by various conservative managements, such as volume replacement.
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