一名患有马凡综合征的年轻患者的巨大主动脉根部动脉瘤：临床影像
Giant Aortic Root Aneurysm in a Young Patient With Marfan Syndrome: A Clinical Image.
作者信息
Bukhari Syed Mohsin Raza, Raza Muhammad Shahzad, Ans Muhammad, Shanza Umema, Abbas Jalil, Yousuf Kamran, Raza Mohsin
机构信息
Department of Medicine Nishtar Medical University and Hospital Multan Pakistan.
Department of Radiology Punjab Institute of Cardiology Lahore Pakistan.
出版信息
Clin Case Rep. 2025 Jul 7;13(7):e70597. doi: 10.1002/ccr3.70597. eCollection 2025 Jul.
Marfan syndrome predisposes individuals to severe cardiovascular complications, including aortic root aneurysms, with a high rupture risk. Timely diagnosis through advanced imaging and surgical intervention, such as the Bentall procedure, is essential. A high level of suspicion should be maintained for cardiovascular complications, even in young individuals with connective tissue disorders.
马凡综合征使个体易患严重的心血管并发症，包括主动脉根部瘤，破裂风险很高。通过先进的影像学检查和手术干预（如Bentall手术）及时诊断至关重要。即使在患有结缔组织疾病的年轻个体中，也应高度怀疑心血管并发症。
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