Kevin R An, Lamia Harik, Talal Alzghari, Roberto Perezgrovas-Olaria, Giovanni Jr Soletti, Arnaldo Dimagli, Gianmarco Cancelli, Mario F L Gaudino, Sharif H Ellozy, Christopher Lau
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Abstract
Subclavian artery aneurysms are rare and can result in thromboembolism or rupture. We present the case of a 41-year-old man with a history of Marfan's syndrome and multiple previous operations, who presented with an enlarging asymptomatic 5.2 cm right subclavian artery aneurysm and was successfully treated with a hybrid surgical operation.
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