지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2009.1
- 수록면
- 448 - 451 (4page)
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초록· 키워드
오류제보하기
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a familial cardiac arrhythmia that is related to
RYR2 or CASQ2 gene mutation. It occurs in patients with structurally normal heart and causes exercise-emotiontriggered
syncope and sudden cardiac death. We experienced a case of CPVT in an 11 year-old female patient who
was admitted for sudden cardiovascular collapse. The initial electrocardiogram (ECG) on emergency department
revealed ventricular fibrillation. After multiple defibrillations, sinus rhythm was restored. However, recurrent
ventricular fibrillation occurred during insertion of nasogastric tube without sedation in coronary care unit. On ECG
monitoring, bidirectional ventricular tachycardia occurred with sinus tachycardia and then degenerated into
ventricular fibrillation. To our knowledge, there has been no previous case report of CPVT triggered by sinus
tachycardia in Korea. Therefore, we report the case as well as a review of the literature.
목차
등록된 정보가 없습니다.
참고문헌 (12)
참고문헌 신청
Coumel P / 1978 / Catecholaminergic- induced severe ventricular arrhythmias with Adams- Stokes syndrome in children: report of four cases / Br Heart J 40 : 28 ~ 37
George CH / 2003 / Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes / Circ R
Gupta A / 2007 / Current concepts in the mechanisms and management of druginduced QT prolongation and torsade de pointes / Am Heart J 153 : 891 ~ 899
Lahat H / 2001 / A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in
Laitinen PJ / 2001 / Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia / Circulation 103 : 485 ~ 490
George CH / 2003 / Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes / Circ R
Gupta A / 2007 / Current concepts in the mechanisms and management of druginduced QT prolongation and torsade de pointes / Am Heart J 153 : 891 ~ 899
Lahat H / 2001 / A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in
Laitinen PJ / 2001 / Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia / Circulation 103 : 485 ~ 490
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