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Başlık: Case of tetralogy of Fallot associated with hypoplasia of the right pulmonary artery - The right internal mammary artery as an aortopulmonary collateral artery in tetralogy of Fallot
Yazarlar: Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Kardiyolojisi Anabilim Dalı.
Bostan, Özlem B.
Çil, Ergün
AAH-3865-2021
AAG-9324-2021
8676936500
35587943300
Anahtar kelimeler: Cardiovascular system & cardiology
Radiology, nuclear medicine & medical imaging
Aortopulmonary collateral artery
Internal mammary artery
Tetralogy of fallot
Scimitar-syndrome
Absence
Yayın Tarihi: Ağu-2005
Yayıncı: Springer
Atıf: Bostan, Ö. M. ve Çil, E. (2005). "Case of tetralogy of Fallot associated with hypoplasia of the right pulmonary artery - The right internal mammary artery as an aortopulmonary collateral artery in tetralogy of Fallot". International Journal of Cardiovascular Imaging, 21(4), 369-371.
Özet: A three-month-old girl was referred to pediatric cardiology unit for evaluation of mild cyanosis and murmur. Chest roentgenogram revealed a boot-shaped heart. Echocardiography demonstrated subaortic ventricular septal defect, aortic override and infundibular stenosis. Then, the patient diagnosed as tetralogy of Fallot (TOF). Cardiac catheterization and angiocardiography revealed infundibular narrowing, hypoplasia of the right pulmonary artery and the enlarged right internal mammary artery originating from the right subclavian artery supplied blood flow into the right lung. The patient was performed complete repair. Post-operative period was uneventful. This is the first report presented about a case which pulmonary blood flow is provided by the enlarged right internal mammary artery in TOF associated with hypoplasia of the right pulmonary artery.
URI: https://doi.org/10.1007/s10554-004-7983-1
https://link.springer.com/article/10.1007%2Fs10554-004-7983-1
http://hdl.handle.net/11452/25015
ISSN: 1569-5794
1573-0743
Koleksiyonlarda Görünür:PubMed
Scopus
Web of Science

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