| Literature DB >> 31577745 |
Huai-Dong Chen1, Fan He, Xi-Ming Qian.
Abstract
RATIONALE: Marfan syndrome (MFS), an autosomal dominant hereditary disease, often results in structural and functional abnormalities of the aortic wall. Because of residual aortic aneurysm or aortic dissection, patients with MFS usually need repeat operations after the first operation. PATIENT CONCERNS: A patient diagnosed with MFS who had undergone 2 surgeries because of abdominal aortic dissection aneurysm and Stanford A type aortic dissection at different times. DIAGNOSES: MFS.Entities:
Mesh:
Year: 2019 PMID: 31577745 PMCID: PMC6783246 DOI: 10.1097/MD.0000000000017391
Source DB: PubMed Journal: Medicine (Baltimore) ISSN: 0025-7974 Impact factor: 1.889
Figure 1A: The first CTA (2005) revealed an abdominal aortic aneurysm dissection. B: The second CTA (2012) revealed a sign of Stanford type A aortic dissection. C: The third CTA revealed an aneurysmal dilatation of the descending aorta.
Figure 2A: The first stent was inserted with the proximal end anchored firmly. B: The second stent was inserted and well positioned. C: Two stents were inserted successfully, and angiography demonstrated that the thoracic aortic aneurysm had disappeared and had no internal leakage.