Case Report: The Parkes-Weber syndrome in the patient who underwent coronary surgery
Nemanja Milosevic, Bogdan Okiljevic, Slobodan Micovic, Milovan Bojic, Igor Zivkovic

TL;DR
This case report describes a 73-year-old man with Parkes-Weber Syndrome and coronary disease who underwent heart surgery.
Contribution
The report highlights the importance of identifying Parkes-Weber Syndrome in patients with heart disease to avoid complications.
Findings
Parkes-Weber Syndrome can coexist with coronary artery disease and impact heart function.
Surgical management is possible in patients with PWS and borderline heart function.
Early diagnosis of PWS is crucial to prevent high-output heart failure.
Abstract
Parkes-Weber Syndrome is a rare congenital vascular abnormality characterized by aneurismatic illness of blood arteries in the afflicted limb, as well as hypertrophy, ulceration, ischemia, and high-output heart failure. Imaging investigations are required to provide a diagnosis, with contrast arteriography being the gold standard. The majority of treatment options are endovascular, with surgical excision for arteriovenous malformations and limb amputation as alternatives. We describe a 73-year-old male patient with mainly asymptomatic PWS, coronary disease, and borderline EF (45%) who had CABG surgery. In individuals with established CAD and other cardiac disorders, it is critical to identify additional diseases or syndromes that might have a compounding effect on the heart, such as PWS and high-output heart failure.
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Taxonomy
TopicsCardiac tumors and thrombi · Congenital Heart Disease Studies · Vascular anomalies and interventions
