Abdominal aortic aneurysm healed with calcification in a female patient with Behçet's syndrome: A case report with a 2-decade follow-up.

Int J Rheum Dis

Division of Rheumatology, Department of Internal Medicine, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey.

Published: January 2024

AI Article Synopsis

  • Abdominal aortic aneurysms (AAA) are uncommon in Behçet syndrome, but they can lead to serious complications and are typically treated with surgery and immunosuppressive therapy.
  • A case study of a female patient who developed a large saccular aneurysm after her Behçet syndrome diagnosis shows that surgery was not an option for her, so she only received immunosuppressive treatment.
  • Remarkably, after two years, the aneurysm size decreased, with signs of wall calcification and no rupture over a 20-year follow-up, suggesting that some large, calcified AAAs may not require surgery and can be monitored safely.

Article Abstract

Abdominal aortic aneurysms (AAA) are rare in Behçet syndrome (BS) but may result in life-threatening complications. AAA are generally treated with surgical intervention following aggressive immunosuppressive therapy. Healing with wall calcification and mural thrombus for AAA is scarcely reported in the literature. Herein, we present a female patient who developed a large saccular aneurysm in the infra-renal abdominal aorta 6 months after the diagnosis. Endovascular intervention was not found to be possible because of the dimensions of the aneurysm and the patient did not consent for open surgery. Therefore, she received only immunosuppressive treatment. By the second year of follow-up, we detected reduction in the size of AAA, along with circumferential wall calcification and mural thrombus. The patient was followed-up for 20 years without rupture and currently doing well. This case demonstrates that calcified large saccular AAA might not necessitate surgical intervention and be followed-up for many years without any complication.

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Source
http://dx.doi.org/10.1111/1756-185X.14859DOI Listing

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