ReviewThe American journal of case reports2021
Aortic Angiosarcoma in Association with Endovascular Aneurysm Repair: Case Report and Review of the Literature.
Review in The American journal of case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 14 citations in OpenAlex.
- Primary Angiosarcoma of the Abdominal Aorta Following Endovascular Aneurysm Repair Mimicking Vascular Graft Infection.Diagnostics (Basel, Switzerland) · 2026Article
- Angiosarcoma of the abdominal aorta after previous endovascular aneurysm repair.Journal of vascular surgery cases and innovative techniques · 2025Article
- Case Series: Natural History and Treatment of Thoracic Aortic Sarcoma.Journal of surgical oncology · 2025Article
- Rectal Angiosarcoma: A Case Report Highlighting Multidisciplinary Strategies for Rare Malignancies.Reports (MDPI) · 2025Article
- Ruptured aortic aneurysm with previous endovascular aneurysm repair in a patient with high-grade angiosarcoma.Journal of vascular surgery cases and innovative techniques · 2024Article
- Article
- Rapid Progression of Angiosarcoma in a Man with a Left Psoas Muscle Hematoma and a Recent EVAR of Abdominal Aorta.Maedica · 2023Article
Corrections and comments
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Authors and funding
7 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND Primary aortic sarcoma often poses diagnostic challenges for pathologists and clinicians because of a very low incidence and controversy over nomenclature and definition. We report a case of aortic angiosarcoma in association with a graft. We also conducted a clinicopathological review of cases of primary aortic sarcomas associated with implanted grafts. CASE REPORT The patient was an 82-year-old woman. She underwent thoracic endovascular aneurysm repair (TEVAR) at age 78 because of an aneurysm in the descending aorta. Approximately 4 years after the TEVAR, computed tomography revealed a type II endoleak and expansion of the aneurysm. Her c-reactive protein level rose to 34 mg/dL, and Ga scintigraphy showed 67Ga accumulation at the aneurysm. She had fever up to 39°C, and a stent graft infection was suspected. Despite administration of antibiotics, her condition deteriorated, and she died. Postmortem examination identified epithelioid aortic angiosarcoma at the aorta with aneurysm repair and the graft, and the aortic angiosarcoma invaded the left lower lobe of the lung. CONCLUSIONS Our clinicopathological review revealed that the proper clinical diagnosis was very difficult owing to confusion of aortic sarcoma after the implantation with the infected graft, atypical endoleak, or pseudoaneurysm. The histological diagnosis was ambiguous because immunohistochemical and genetic studies were not adequately conducted. Overall prognosis of aortic sarcoma is poor as most patients die within a year, with no effective treatments. It is hoped that recent projects for genomic medicine will provide useful insights about the diagnosis and treatment of these cancers.
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