Concealed congenital long QT syndrome during velopharyngeal dysfunction correction: a case report
전소은, 이현정, 정영훈, 도왕석, 조아름, 백지석, 이도원, 김은정, 김은수, 홍정민,
소속 상세정보
전소은 ( Jeon So-Eun ) - Pusan National University School of Medicine Department of Anesthesia and Pain Medicine
이현정 ( Lee Hyeon-Jeong ) - Pusan National University School of Medicine Department of Anesthesia and Pain Medicine
정영훈 ( Jung Young-Hoon ) - Pusan National University School of Medicine Department of Anesthesia and Pain Medicine
도왕석 ( Do Wang-Seok ) - Pusan National University School of Medicine Department of Anesthesia and Pain Medicine
조아름 ( Cho Ah-Reum ) - Pusan National University School of Medicine Department of Anesthesia and Pain Medicine
백지석 ( Baik Ji-Seok ) - Pusan National University School of Medicine Department of Anesthesia and Pain Medicine
이도원 ( Lee Do-Won ) - Pusan National University School of Medicine Department of Anesthesia and Pain Medicine
김은정 ( Kim Eun-Jung ) - Pusan National University School of Dentistry Department of Dental Anesthesia and Pain Medicine
김은수 ( Kim Eun-Soo ) - Pusan National University School of Medicine Department of Anesthesia and Pain Medicine
홍정민 ( Hong Jeong-Min ) - Pusan National University School of Medicine Department of Anesthesia and Pain Medicine
Abstract
The congenital long QT syndrome (LQTS) is an inherited cardiac disorder characterized by increased QT intervals and a tendency to experience ventricular tachycardia, which can cause fainting, heart failure, or sudden death. A 4-year-old female patient undergoing velopharyngeal correction surgery under general anesthesia suddenly developed Torsades de pointes. Although the patient spontaneously resolved to sinus rhythm without treatment, subsequent QT prolongation persisted. Here, we report a case of concealed LQTS with a literature review.
키워드
Electrocardiogram; Long QT Syndrome; Torsades de Pointes
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