Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy A case report

Abstract

Rationale: Myotonic dystrophy is a progressive multisystem genetic heterogeneous disorder. General anesthesia with opioids increases the risk of prolonged postanesthetic respiratory recovery in myotonic dystrophy patients. Patient concerns: A 20-year-old previously healthy woman was transferred to our emergency department for further workup of respiratory failure, and massive ascites with abscess caused by endometriosis. Hypercapnic respiratory failure persisted under intensive care unit (ICU) management, but finally improved after cessation of fentanyl as a sedative agent. Diagnosis: Myotonic dystrophy type 1. Interventions: Massive ascites with abscess was accordingly managed by drainage, antibiotics, and an antifungal agent. Myotonic dystrophy type 1 was confirmed after molecular genetic testing revealed a cytosine-thymine-guanine repeat length of 400 to 450 in the DMPK gene. Outcomes: The patient was discharged without complications on hospital day 69. Lessons: Myotonic dystrophy should be considered when hypercapnic respiratory failure persists in sedated ICU patients. Opioids should not be used for perioperative management of patients with myotonic dystrophy. Abbreviations: CO2 = carbon dioxide, CT = computed tomography, CTG = cytosine-thymine-guanine, ICU = intensive care unit, MD = myotonic dystrophy, MG = myasthenia gravis, MRI = magnetic resonance imaging.