A rare cause of rhabdomyolysis and acute renal failure in an adult patient: Carnitine palmitoyltransferase II deficiency
Acta Medica Mediterranea, cilt.33, sa.5, ss.789-793, 2017 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 33 Sayı: 5
- Basım Tarihi: 2017
- Doi Numarası: 10.19193/0393-6384_2017_5_116
- Dergi Adı: Acta Medica Mediterranea
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.789-793
- Anahtar Kelimeler: Acute renal failure, Carnitine palmitoyl transferase II deficiency, Rhabdomyolysis
- Sağlık Bilimleri Üniversitesi Adresli: Evet
Özet
Introduction: Inherited metabolic disorders are the most common causes of recurrent rhabdomyolysis in adults and children. Carnitine palmitoyltransferase II (CPT II) deficiency is the most common inherited lipid metabolism disorder resulting in recurrent myoglobinuria. CPT II deficiency is inherited in an autosomal recessive trait and clinical phenotype varies from severe and multisystemic infantile form to mild muscle form characterized by rhabdomyolysis and myoglobinuria. Exercise, infections, starvation, and cold exposure are the most important factors triggering rhabdomyolysis in cases with CPT II deficiency. The severity of disease episodes is considerably variable and some patients may develop acute renal failure during the episodes. Case presentation: The current manuscript presents a patient with acute uremia, who suffered from nausea, vomiting, and dark-colored urination in the past three days. The patient was initially considered to have acute renal failure (ARF) associated with dehydration. However, high levels of creatine phosphokinase suggested the diagnosis of rhabdomyolysis. Remarkable medical history for prolonged starvation and cold exposure and past medical history that was remarkable for a single episode of dark-colored urination in adolescence prompted genetic analysis, which revealed carnitine palmitoyltransferase II(CPT II) deficiency. The current report presents a patient with acute renal failure secondary to rhabdomyolysis that was associated with CPT II deficiency and it highlights the importance of anamnesis in diagnosis and treatment. Conclusion: Inherited disorders are one of the rare but important causes of rhabdomyolysis. These inherited causes are often overlooked. The present manuscript has attempted to highlight these issues.