The current paper presents a case of a patient with pectus excavatum deformity who had a new surgical approach to the Bentall surgery. A middle-aged guy was diagnosed with Marfan syndrome and pectus excavatum, and he was experiencing chest pain and dyspnea. Chest X-ray, transthoracic echocardiography, and computed tomography (CT) of the heart and aorta indicated significant aortic regurgitation with dilated aortic root, sinotubular junction, ascending aorta, and descending thoracic aorta. It was decided to have surgery. Due to Pectus excavatum, heart exposure and cannulation for cardiopulmonary bypass were problematic. We successfully completed the femoro-femoral bypass for ahesiolysis and the Bentall surgery. The patient's postoperative stay was unremarkable, and he was followed up on at regular intervals. Because Marfan syndrome is linked to a variety of illnesses that impact several body systems, each patient must be treated as an individual.
Author(S) Details
Subrata Pramanik
Department of Cardiothoracic and Vascular Surgery, GB Pant Hospital (GIPMER), New Delhi, India.
Ajit Padhy
Department of Cardiothoracic and Vascular Surgery, GB Pant Hospital (GIPMER), New Delhi, India.
Nayem Raja
Department of Cardiothoracic and Vascular Surgery, GB Pant Hospital (GIPMER), New Delhi, India.
Subodh Satyarthy
Department of Cardiothoracic and Vascular Surgery, GB Pant Hospital (GIPMER), New Delhi, India.
View Book:- https://stm.bookpi.org/IDMMR-V7/article/view/5764
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