A Severe and Fatal Type A Aortic Dissection in an Adult with a Repaired Tetralogy of Fallot.

Q4 Biochemistry, Genetics and Molecular Biology
Manuela Montatore, Federica Masino, Vincenzo Signorile, Marina Balbino, Ruggiero Tupputi, Giuseppe Guglielmi
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引用次数: 0

Abstract

We report a case of a 44-year-old woman surgically treated for tetralogy of Fallot who experienced an acute and extensive Stanford A type aortic dissection despite the meticulous follow-up. While aortic dilatation is prevalent in individuals with repaired tetralogy of Fallot, aortic dissection represents a rare consequence, that when it appears, is progressive and usually detected during the check-up visits. In the case reported, the dissection was unexpected and severe, and the patient's clinical state worsened suddenly, leading to death after a few days. Constant awareness for aortic aneurysms is essential in the Fallot tetralogy population, nevertheless, several causes may contribute to the acute worsening of the clinical condition until the patient's death.

一名法洛氏四联症修复成人的严重致命 A 型主动脉夹层。
我们报告了一例接受法洛氏四联症手术治疗的 44 岁女性病例,尽管她接受了精心的随访,但还是发生了急性、广泛的斯坦福 A 型主动脉夹层。虽然法洛氏四联症患者的主动脉扩张在修复后的患者中很常见,但主动脉夹层是一种罕见的后果,一旦出现,会逐渐发展,通常在检查时被发现。在报告的病例中,主动脉夹层是意料之外的严重后果,患者的临床状态突然恶化,几天后死亡。在法洛氏四联症患者中,时刻警惕主动脉瘤是非常重要的,然而,多种原因都可能导致患者的临床状况急剧恶化,直至死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Prague medical report
Prague medical report Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
19
审稿时长
20 weeks
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