临床病例:Bentall De Bono,主动脉动脉瘤和马凡氏综合征患者的首选技术

Karen Michelle Novo Pinos, Javier Arturo López Rodríguez, Luis Alfredo Rodríguez Rodríguez, Juan Bernardo Flores Siguenza, Andrés Fernando Cajamarca Taza
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引用次数: 0

摘要

背景:马凡氏综合征患者发生主动脉变性的风险高于其他人群,表现为动脉瘤、破裂和夹层。尽管本特尔手术被认为是主动脉瓣和升主动脉合并疾病手术治疗的金标准;传统上,马凡氏综合征患者的主动脉表现采用开放手术技术修复,因为这种患者的血管内修复仍然存在争议。病例报告:我们描述的情况下,患者马凡氏综合征的历史和诊断严重的主动脉狭窄和主动脉瘤,需要一个先进的和高专业的外科手术的解决方案,并考虑到他的合并症所带来的困难。进展:本特尔/德博诺手术与机械主动脉瓣置换术成功;然而,经手术出血3 600毫升。患者需要起搏器支持,血管加压剂支持和血液制品管理。在ICU住院期间,患者出现肺脓毒症,经广谱抗生素治疗,住院62天后病情完全好转。出院后,患者继续随访,迄今未发生与基础疾病相关的新并发症。结论:由于科学的进步,马凡氏综合征患者的主动脉瘤手术修复已经得到了发展,正如本病例所证明的那样,手术死亡率降低,并提高了这种潜在病理患者的质量和预期寿命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Caso Clínico: Bentall De Bono, técnica de elección para paciente con aneurisma de aorta y síndrome de Marfan
BACKGROUND: Patients with Marfan syndrome have a higher risk of aortic degeneration than the rest of the population, presenting with aneurysms, ruptures and dissections. Although the Bentall procedure has been considered the gold standard in the surgical treatment of combined diseases of the aortic valve and ascending aorta; traditionally, aortic manifestations in patients with Marfan syndrome are repaired with open surgical techniques, since endovascular repair in this patients is still controversial. CASE REPORT: We describe the case of a patient with a history of Marfan syndrome and a diagnosis of severe aortic stenosis and aortic aneurysm, in need of an advanced and high expertise surgical procedure for its resolution and considering the difficulty given by his comorbidity. EVOLUTION: Bentall/De Bono surgery with mechanical aortic valve replacement was successfully performed; however, there was a trans-surgical bleeding of 3 600 ml. The patient required pacemaker support, vasopressor support, and administration of blood products. During his hospitalization in the ICU, he presented with pulmonary sepsis, treated with broad-spectrum antibiotics, with complete resolution of the condition after 62 days of hospitalization. After being discharged, he remained in follow-up, with no new complications related to his underlying disease to date. CONCLUSION: Surgical repair of aortic aneurysms in patients with Marfan syndrome has evolved thanks to scientific advances, as evidenced in this case, achieving a decrease in surgical mortality rate and improving the quality and life expectancy of patients with this underlying pathology.
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