Zobrazeno 1 - 10
of 729
pro vyhledávání: '"ALCAPA"'
Autor:
Lam Truong Hoai, MD, Nguyen Van Thanh, MD, Nguyen Cong Thanh, MD, Nguyen Duc Hung, MD, Tran Duc Minh, MD, Nguyen Tuan Long, MD
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 570-573 (2025)
ALCAPA is a rare congenital anomaly that presents with left ventricular (LV) dysfunction and mitral valve regurgitation. The mortality rate is roughly 90% if the intracoronary collateral isn't significantly augmented. Malignant arrhythmias resulting
Externí odkaz:
https://doaj.org/article/f865ba4ebd3241d5aafccb0a84ddacfe
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-5 (2024)
Abstract Background Anomalous left coronary artery originating from the pulmonary artery (ALCAPA), is a unique congenital anomaly, comprising only 0.24–0.46% of all congenital cardiac anomalies. Late presentations, ranging from asymptomatic cases t
Externí odkaz:
https://doaj.org/article/08868b3eeb6f43dfbd45e4a172067061
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Aberrant left coronary artery from pulmonary artery (ALCAPA) is a very rare congenital heart defect. Its coexistence with patent ductus arteriosus (PDA) is extremely rare. The high pressures created by the left-to-right shunt in t
Externí odkaz:
https://doaj.org/article/9a25151697b3427e97e1b04422e2eb07
Autor:
Josu Erquicia Peralt, Larraitz Orive Melero, Jagoba Larrazabal López, José Félix Larrea Egurbide, Eugenia García Fernández, Luis Fernández González, Roberto Blanco Mata, Josune Arriola Meabe
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 19, Iss , Pp 100553- (2025)
Introduction: Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital heart disease that in most cases manifests in the first months of life, being a well-studied entity of myocardial ischaemia in young pa
Externí odkaz:
https://doaj.org/article/58c32caede7e40beaccc6af433340827
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiac anomaly, mortality rates in infancy reach approximately 90%, with only a small number of patients surviving into adulthoo
Externí odkaz:
https://doaj.org/article/fcbf739a00604df2a8a1f5c44d1b6756
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 7, p 219 (2024)
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare and potentially life-threatening condition affecting infants that requires immediate corrective surgery to restore blood flow to the myocardium. We present a ca
Externí odkaz:
https://doaj.org/article/ece9994a722c46158eb46ca61092f50d
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 15, Iss 3, Pp 181-185 (2023)
ALCAPA is a rare congenital heart disease. Presentation varies from asymptomatic to progressive heart failure and death. Surgical repair is indicated in all patients with a goal of restoring two coronary systems. Data was analysed in regard to presen
Externí odkaz:
https://doaj.org/article/e07dfec7a5f44bcc8f577eaa16bdb028
Autor:
Takeo Mukai, Kenji Waki
Publikováno v:
Clinical Case Reports, Vol 11, Iss 8, Pp n/a-n/a (2023)
Key Clinical Message ALCAPA should be considered in the differential diagnosis of myocarditis, and contrast‐enhanced CT or catheterization should be considered even if coronary artery abnormalities are not detected on echocardiography.
Externí odkaz:
https://doaj.org/article/5ceccec1b9c348d8888827f486195981
Publikováno v:
The Cardiothoracic Surgeon, Vol 30, Iss 1, Pp 1-4 (2022)
Abstract Background Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly that typically presents within the first year of life but can also sporadically present in adults. ALCAPA, if left untreated, can lead
Externí odkaz:
https://doaj.org/article/0d59dc2fab0340c88e991c06f4413ecf
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