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World J Pediatr Congenit Heart Surg ; 11(5): 661-663, 2020 09.
Article in English | MEDLINE | ID: mdl-32853077

ABSTRACT

We report long-term outcome after two-stage, "one lung repair" in a four-year-old boy with tetralogy of Fallot and congenital absence of the left pulmonary artery. The operation was carried out two years after a palliative aortopulmonary central shunt and was uneventful. Twenty-six years later, the patient is in excellent clinical condition, with normal peripheral oxygen saturation. A recent radionuclide lung scan and cardiac magnetic resonance imaging show the pulmonary flow entirely directed into the right lung. In selected cases, the long-term prognosis of patients with tetralogy of Fallot and true absence of left pulmonary artery after "one lung repair" may be excellent.


Subject(s)
Cardiac Surgical Procedures/methods , Forecasting , Pulmonary Artery/abnormalities , Tetralogy of Fallot/surgery , Angiography , Child, Preschool , Echocardiography , Follow-Up Studies , Humans , Male , Prognosis , Pulmonary Artery/surgery , Tetralogy of Fallot/diagnosis
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