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Epithelioid Angiosarcoma after EVAR. A Case Report
Boris Cleret de Langavant1, Alexandros Nicolaou Flaris2, Denis Dasnoy3
1Department of Digestive Surgery, Cliniques Universitaires St-Luc Université Catholique de Louvain, Brussels, Belgium.
A rare case of epithelioid angiosarcoma developed after endovascular aneurysm repair (EVAR). Diagnosis was challenging, highlighting the need to consider aortic tumors in EVAR patients with evolving aneurysm morphology.
Area of Science:
- Vascular Surgery
- Surgical Oncology
- Diagnostic Imaging
Background:
- Endovascular aneurysm repair (EVAR) is a standard treatment for aneurysms, but complications can arise.
- Endoleaks are the most frequent complication, while graft infection diagnosis can be difficult.
- Epithelioid angiosarcoma is an uncommon malignancy that can occur post-EVAR.
Observation:
- A 64-year-old male presented with pain and aneurysm recurrence four years after EVAR.
- Imaging revealed aneurysm recurrence and abnormal tracer uptake, but no signs of graft infection.
- Histological analysis of the explanted endograft confirmed epithelioid angiosarcoma.
Findings:
- The patient developed epithelioid angiosarcoma following EVAR.
- Diagnostic imaging, including CT angiography and FDG-PET-CT, presented challenges in identifying the malignancy.
- Despite treatment, the patient's outcome was poor.
Implications:
- Consider aortic tumors in EVAR patients with morphological changes in the aortic wall or aneurysm sac.
- This case underscores the diagnostic challenges associated with rare post-EVAR malignancies.
- Early recognition and consideration of rare complications are crucial for patient management.
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