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Acute Quadriplegic Myopathy in a 17-Month-Old Boy

Department of Pediatrics University of Padua

Anna Maria Laverda, MD

Department of Pediatrics University of Padua

Lucia Zancan, MD

Department of Pediatrics University of Padua

Marina Fanin, PhD

Regional Neuromuscular Diseases Center Department of Neurological and Psychiatric Sciences University of Padua Padua, Italy

Corrado Angelini, MD

Regional Neuromuscular Diseases Center Department of Neurological and Psychiatric Sciences University of Padua Padua, Italy

Mija Meznaric-Petrusa, MD

Institute of Anatomy University of Ljubljana Ljubljana, Slovenia

Acute quadriplegic myopathy is a rare condition associated with the use of nondepolarizing muscle-blocking agents and corticosteroids in the course of severe systemic illness. A 17-month-old boy underwent liver transplantation for fulminant hepatitis. He was intubated for 24 days and treated with vecuronium bromide and high-dose methylprednisolone. The child was weaned from the ventilator and presented extreme weakness in the upper limbs and total paralysis of the lower limbs. Serum creatine kinase level was normal and electromyography showed myopathic abnormalities. Muscle biopsy showed severe type-1 fiber atrophy and selective loss of myosin thick filaments was seen on electron microscopy. Scattered regenerating fetal myosin-positive fibers were present, µ calpain was absent, while m calpain was diffusely expressed. Physical therapy was immediately started and the child recovered even though corticosteroids were not discontinued. The pathogenesis of acute quadriplegic myopathy is still unknown. We suggest that it could be due to abnormal protein turnover in the muscle. Several independent factors, such as corticosteroid treatment, immobilization, or cytokines, could take part in a cascade of events that leads to an excessive yet selective degradation of proteins involving myosin thick filaments and possibly components of sarcolemma, causing muscle inexcitability. (J Child Neurol 2000;15:63-66).

Journal of Child Neurology, Vol. 15, No. 1, 63-66 (2000)
DOI: 10.1177/088307380001500115


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