Aortic Thrombosis Occurring in a Patient with Behçet Disease and Multiple Thrombophilias: A Case Report

Abstract Behçet disease represents an inflammatory condition capable of affecting blood vessels in both venous and arterial circulations, a clinical pattern like the one encountered in antiphospholipid syndrome, although disease mechanisms differ. This case report presents the occurrence of an acute episode of paraparesis due to aortic thrombosis in a patient with a known history of Behçet disease, treated by way of a thromboembolectomy. There were no systemic inflammatory syndrome or other suggestive symptoms for a relapse of the patient’s underlying condition. A hypercoagulable workup revealed the presence of several prothrombotic factors, including antithrombin III and protein S deficiencies, alongside the confirmation of a positive lupus anticoagulant. This case highlights the clinical challenge that the aortic thrombosis posed, which was finally attributed to the particular association of prothrombotic factors, in a patient with an apparently inactive Behçet disease and an antiphospholipid syndrome that had probably played the most significant role in the acute presentation.

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Publication Details

Journal
Internal Medicine
Published
2025-06-01
DOI
https://doi.org/10.2478/inmed-2025-0328
Primary Topic
Ocular Diseases and Behçet’s Syndrome
Type
article
Field-Weighted Citation Impact
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article

Aortic Thrombosis Occurring in a Patient with Behçet Disease and Multiple Thrombophilias: A Case Report

Internal Medicine
Ocular Diseases and Behçet’s Syndrome
article

Aortic Thrombosis Occurring in a Patient with Behçet Disease and Multiple Thrombophilias: A Case Report

article en

Abstract

Abstract Behçet disease represents an inflammatory condition capable of affecting blood vessels in both venous and arterial circulations, a clinical pattern like the one encountered in antiphospholipid syndrome, although disease mechanisms differ. This case report presents the occurrence of an acute episode of paraparesis due to aortic thrombosis in a patient with a known history of Behçet disease, treated by way of a thromboembolectomy. There were no systemic inflammatory syndrome or other suggestive symptoms for a relapse of the patient’s underlying condition. A hypercoagulable workup revealed the presence of several prothrombotic factors, including antithrombin III and protein S deficiencies, alongside the confirmation of a positive lupus anticoagulant. This case highlights the clinical challenge that the aortic thrombosis posed, which was finally attributed to the particular association of prothrombotic factors, in a patient with an apparently inactive Behçet disease and an antiphospholipid syndrome that had probably played the most significant role in the acute presentation.

Internal MedicineVol. 22(2)
Carol Davila University of Medicine and Pharmacy (RO), Emergency University (US), Spitalul Clinic Colentina (RO)
Good health and well-being
Openalex Percentile: Top 36%
Ocular Diseases and Behçet’s Syndrome
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