Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Mini-Focus Issue: Congenital Heart Disease"'
Autor:
Massimo Caputo, Iakovos Ttofi, Filippo Rapetto, Mark W. Lowdell, Qiang Chen, Demetris Taliotis, Serban Stoica, B. Weil, Paolo Madeddu, Dominga Iacobazzi
Publikováno v:
JACC: Case Reports, Vol 3, Iss 5, Pp 724-727 (2021)
Rapetto, F 2021, ' Allogeneic Mesenchymal Stromal Cell Injection to Alleviate Ischemic Heart Failure Following Arterial Switch Operation. ', JACC: Case Reports, vol. 3, no. 5, pp. 724-727 . https://doi.org/10.1016/j.jaccas.2021.02.039
Jacc. Case Reports
Rapetto, F 2021, ' Allogeneic Mesenchymal Stromal Cell Injection to Alleviate Ischemic Heart Failure Following Arterial Switch Operation. ', JACC: Case Reports, vol. 3, no. 5, pp. 724-727 . https://doi.org/10.1016/j.jaccas.2021.02.039
Jacc. Case Reports
Cell therapy is a promising tool to prevent and treat heart failure in congenital heart disease. We report the first case of intramyocardial injection of allogeneic mesenchymal stromal cells as rescue therapy in a neonate with ischemic heart failure
Autor:
Yoichi Takaya, Shingo Kasahara, Norihisa Toh, Nobuhisa Watanabe, Teiji Akagi, Hiroshi Ito, Fumi Yokohama, Yasuhiro Kotani
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 3, Iss 5, Pp 731-735 (2021)
JACC: Case Reports, Vol 3, Iss 5, Pp 731-735 (2021)
Takeuchi repair is a unique surgical approach in anomalous left coronary artery from the pulmonary artery. We present an adult patient with anomalous left coronary artery from the pulmonary artery with multiple late structural complications after Tak
Autor:
Yuhei Shiga, Tomoki Imaizumi, Shin-ichiro Miura, Kohei Takata, Makoto Sugihara, Akira Matsunaga, Amane Ike, Yoshiaki Idemoto
Publikováno v:
JACC: Case Reports, Vol 3, Iss 5, Pp 740-744 (2021)
JACC Case Reports
JACC Case Reports
An asymptomatic patient presented at our hospital exhibiting a Brugada electrocardiography pattern with coronary artery fistulas. Coronary artery fistula is a congenital or acquired rare abnormal condition with increased symptoms and complications ov
Chylothorax Due to Superior Vena Cava Obstruction in a Patient With Complex Congenital Heart Disease
Autor:
Assunta Merola, Flavia Fusco, Nunzia Borrelli, Berardo Sarubbi, Rosaria Barracano, Giacomo Sica, Anna Correra, Giancarlo Scognamiglio, Giovanni Domenico Ciriello, Michela Palma
Publikováno v:
JACC: Case Reports, Vol 3, Iss 5, Pp 736-739 (2021)
JACC Case Reports
JACC Case Reports
Obstruction of the superior vena cava represents an under-recognized cause of chylothorax in the adult population. Our case report describes the successful conservative management of chylothorax due to bilateral superior vena cava obstruction in an a
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 3, Iss 2, Pp 194-197 (2021)
JACC: Case Reports, Vol 3, Iss 2, Pp 194-197 (2021)
A 21-year-old man presented with new-onset seizures and brain abscess. Echocardiography and cardiac magnetic resonance imaging revealed underlying Ebstein anomaly, secundum atrial septal defect, and cor triatriatum dexter. The elevated right heart pr
Autor:
Jacek Pająk, Katarzyna Szymańska–Beta, Wojciech Mądry, Jacek Kuźma, Bozena Kociszewska-Najman, Maciej A. Karolczak, Darren James Grégoire, Michał Buczyński
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 3, Iss 2, Pp 220-224 (2021)
JACC: Case Reports, Vol 3, Iss 2, Pp 220-224 (2021)
A newborn with pulmonary hypertension due to the premature fetal arterial duct occlusion was diagnosed with a giant left ventricle thrombus. Cardiopulmonary compromise required multidrug therapy with vasopressors infusions, high-frequency oscillation
Autor:
R. Allen Ligon, Christopher J. Petit
Publikováno v:
JACC: Case Reports, Vol 3, Iss 2, Pp 180-186 (2021)
JACC Case Reports
JACC Case Reports
We describe the use of direct percutaneous cardiac access to recanalize an atretic right pulmonary artery in an adolescent with complex congenital heart disease and right heart failure. This case highlights the problems associated with loss of centra
Autor:
Sigifredo Macossay Santiago, David Salazar Lizárraga, Cristopher German Arroyo, Moisés Jiménez Santos, Horacio Márquez González, Carlos Riera Kinkel, Diana López Gallegos, Lucelli Yáñez Gutiérrez, Israel García Davalos, Jaime Alfonso Santiago Hernández
Publikováno v:
JACC: Case Reports, Vol 3, Iss 2, Pp 202-205 (2021)
JACC Case Reports
JACC Case Reports
We report a man with congenitally corrected transposition of the great arteries and moderate anteroseptal ischemia; and cardiac computed tomography showed a single coronary artery with origin from the right aortic sinus. The perfusion of the morpholo
Autor:
Ponraj Chinnadurai, Michael J. Reardon, Thomas E. MacGillivray, Charudatta S. Bavare, Zhongyu Li, C. Huie Lin, Lamees I. El Nihum
Publikováno v:
JACC: Case Reports, Vol 3, Iss 2, Pp 225-229 (2021)
JACC Case Reports
JACC Case Reports
We describe a 64-year-old woman with subclavian pseudoaneurysm after aortic coarctation repair, treated using a hybrid approach involving true three-dimensional analysis and image fusion-guided placement of thoracic endovascular aortic repair stents.
Autor:
Raghav Murthy, Sarit S. Cohen, Sathiji Nageshwaran, Jennifer L. Cohen, Barry Love, Ali N. Zaidi, Simone Jhaveri, Alice Chan
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 3, Iss 2, Pp 230-235 (2021)
JACC: Case Reports, Vol 3, Iss 2, Pp 230-235 (2021)
Eisenmenger syndrome refers to any untreated congenital cardiac defect with an intracardiac communication that leads to pulmonary arterial hypertension, reversal of intracardiac shunting, and cyanosis. We describe a 40-year-old cyanotic patient with