Central Core Disease: Atypical Case With Respiratory Insufficiency in an Intensive Care Unit
Makaleler > Tam Makale · 2006
Yazarlar: Muzaffer Polat, Ayse Tosun, Yilmaz Ay, Erdener Ozer, Gul Serdaroglu, Sema AYDOĞDU, SARENUR GÖKBEN, Hasan TEKGÜL
Journal of Child Neurology, Uluslararası, Wos, 2006, cilt 21, ss 173-174
DOI: 10.1177/08830738060210021301
Özet
Central core disease is a rare congenital myopathy characterized by formation of typical cores in myofibrils. We report an atypical case of central core disease with respiratory insufficiency in the late stage of congenital myopathy. A 13-year-old girl was admitted to the intensive care unit with the diagnosis of respiratory distress syndrome. Ventilatory support was initiated. After 2 weeks of follow-up, the Division of Pediatric Neurology was consulted owing to the failure to wean her from the ventilator. Clinical and electromyographic features were in favor of primary muscle disease. Muscle biopsy revealed typical cores in type 1 muscle fibers, which were diagnostic for central core disease. This case was presented to emphasize that patients with respiratory distress who cannot be weaned from the ventilator should be evaluated for central core disease with an atypical presentation.