一名年轻的白塞氏病患者的致命胸腹动脉瘤扩张

Bakkali Tarik, H. M. Amine, Lekhel Brahim, Sefiani Yasser, M. Abbes, B. Younes
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引用次数: 0

摘要

白塞氏病的动脉受累已有报道。我们报告一个罕见的病例大而长段胸腹动脉瘤,这是相关的Behcet病,并有一个不利的发展。病例介绍:一名23岁的男性被诊断患有白塞氏病,颈动脉瘤显示,并接受假体移植物重建和免疫抑制治疗。该患者未能随访。出院一个月后,他主动停止服药。两年后,患者出现持续1周的胸痛。通过计算机断层血管造影发现了一个大动脉瘤,它累及肾动脉上方从Valsalva窦到腹主动脉的长主动脉段。不幸的是,尽管进行了免疫抑制治疗,患者还是在任何手术或血管内介入治疗之前死亡。结论:这一罕见的观察结果支持免疫抑制治疗在预防白塞病治疗中危及生命的血管病变复发中的作用。
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Fatal expanding thoracoabdominal aneurysm in known but mistreated behcet's disease in a young patient
Introduction: Arterial involvement in Behcet's disease has been previously described. We report a rare case of a large and longsegment thoracoabdominal aneurysm, which was associated with Behcet's disease and had an unfavorable evolution. Case Presentation: A 23-year-old man was diagnosed with Behcet's disease, as revealed by a carotid aneurysm, and was treated with a prosthetic graft reconstruction as well as immunosuppressive therapy. The patient was lost to follow-up. He stopped the medications of his own will 1 month after his discharge from the hospital. Two years later, he presented with chest pain of 1 week's duration. Alarge aneurysminvolving a long aorta segment from the sinus of Valsalva to the abdominal aorta above the renal arteries was identified by computed tomography angiography. Unfortunately, the patient died despite immunosuppressive therapy and before any surgical or endovascular intervention could be performed. Conclusions: This rare observation supports the role of immunosuppressive therapy in preventing the recurrence of lifethreatening vascular lesions in the management of Behcet's disease.
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