The clinical features, pathological findings, and risk factors of intracardiac thrombus in Behçet’s syndrome
摘要
To investigate the clinical features, pathological findings, and risk factors of intracardiac thrombus (ICT) in Behçet’s syndrome (BS).
MethodsWe conducted a case–control study using our BS registry database. BS patients with ICT were enrolled as the cases, and controls were selected using risk-set-sampling. Multivariable logistic regression identified risk factors, and outcomes were also analyzed. Pathology of six ICT specimens was reanalyzed by preoperative disease activity.
ResultsSeventeen BS patients with ICT (14 males, 3 females, BS onset age: 26.4 ± 8.0 years) were enrolled. Compared to controls, ICT patients had higher venous involvement (70.6% vs. 13.7%, p < 0.001), pulmonary artery thrombosis (64.7% vs. 3.9%, p < 0.001), elevated ESR (26.0 vs. 9.8 mm/h, p = 0.013), CRP (34.7 vs. 10.1 mg/L, p < 0.001), and monocyte count (0.5 vs. 0.4*10^9/L, p = 0.024). Multivariable logistic regression identified CRP > 20 mg/L (OR 11.27, 95% CI 1.13–112.26, p = 0.039) and venous involvement (OR 11.71, 95% CI 2.79–49.20, p < 0.001) as ICT risk factors. Pathology revealed increased infiltration of neutrophils and CD68+macrophages, which was more prominent in active cases. With a follow-up of 35.7 ± 24.8 months, 1- and 3- year survival rates were both 88.2%, and the relapse-free rates were 81.3% and 54.2%.
ConclusionICT in BS is a severe complication with a high relapse rate and pathological features of neutrophils and macrophages’ infiltration. Elevated CRP (> 20 mg/L) and venous involvement are potential risk factors. These findings support the potential benefit of adequate immunosuppressive treatment before surgery for improving outcomes in BS patients with ICT.