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Pulsating suprasternal lump: a diagnostic and management dilemma
Ahmed Sayed1, Alaa Farok, Hosam El-Sayed
1Kasr Alainy Hospital, Cairo University, Cairo, Egypt.
A 70-year-old woman with shortness of breath and a suprasternal lump underwent successful surgical repair for innominate artery dilatation and a common arterial origin. The procedure resolved her symptoms, highlighting effective treatment for this rare vascular anomaly.
Area of Science:
- Cardiovascular Surgery
- Vascular Anomalies
- Thoracic Surgery
Background:
- A 70-year-old female presented with significant symptoms of dyspnea and a palpable suprasternal mass.
- This case highlights a rare congenital vascular anomaly involving the great vessels of the aortic arch.
- The patient's symptoms suggested potential hemodynamic compromise due to the arterial malformation.
Observation:
- Computed Tomography (CT) imaging revealed significant dilatation of the innominate artery.
- Intraoperative findings confirmed tortuous arteries and an unusual common origin of the left common carotid artery and the innominate artery.
- The anatomical variations presented a complex surgical challenge.
Findings:
- Surgical intervention involved the division and subsequent reimplantation of the innominate artery to the ascending aorta.
- This complex reconstructive procedure successfully addressed the arterial malformation.
- Post-operative assessment confirmed complete resolution of the patient's presenting symptoms.
Implications:
- This case demonstrates the feasibility and efficacy of surgical correction for complex innominate artery anomalies.
- Successful surgical management can lead to complete symptom relief and improved quality of life.
- Further research into the long-term outcomes of such rare vascular reconstructions is warranted.
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