Hybrid Coronary Revascularization in Congenital Pericardial Absence: A Case Report.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Corey Badgett, Andrew Winegarner, Geoffrey Hayward
{"title":"Hybrid Coronary Revascularization in Congenital Pericardial Absence: A Case Report.","authors":"Corey Badgett, Andrew Winegarner, Geoffrey Hayward","doi":"10.12659/AJCR.945774","DOIUrl":null,"url":null,"abstract":"<p><p>BACKGROUND Congenital pericardial agenesis is a rare condition that is frequently associated with abnormal intrathoracic anatomy, especially malpositioning of the heart within the thoracic cavity. In the setting of coronary artery bypass, these anatomic derangements can present surgical challenges that can necessitate incorporating complementary, non-surgical solutions for complete revascularization. CASE REPORT A 48-year-old male patient presented with acute anginal symptoms, with workup revealing severe, multivessel coronary artery disease, as well as partial absence of the pericardium. Preoperative imaging revealed a severely displaced heart deep into the left chest. He was subsequently scheduled for coronary artery bypass grafting. However, altered anatomy from the absent pericardium required the procedure to be unexpectedly modified intraoperatively to address displaced coronary vessel targets that were surgically inaccessible. The patient's anterior vessels were grafted without complication, but the lateral and posterior vessels were unable to be grafted, due to excessive manipulation of the heart required for visualization. An intra-aortic balloon pump was utilized to maximize perfusion until a percutaneous coronary intervention could be completed by a cardiologist in these remaining vessels. CONCLUSIONS While congenital pericardial agenesis is a rare condition, the anatomic abnormalities encountered in this case are not uncommon within this patient population. These variances can interfere with standard coronary artery bypass grafting techniques. Understanding the unique challenges present in patients with this condition can aid in preoperative planning and coordination of a multispecialty approach for complicated revascularization.</p>","PeriodicalId":39064,"journal":{"name":"American Journal of Case Reports","volume":"25 ","pages":"e945774"},"PeriodicalIF":1.0000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11666117/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12659/AJCR.945774","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND Congenital pericardial agenesis is a rare condition that is frequently associated with abnormal intrathoracic anatomy, especially malpositioning of the heart within the thoracic cavity. In the setting of coronary artery bypass, these anatomic derangements can present surgical challenges that can necessitate incorporating complementary, non-surgical solutions for complete revascularization. CASE REPORT A 48-year-old male patient presented with acute anginal symptoms, with workup revealing severe, multivessel coronary artery disease, as well as partial absence of the pericardium. Preoperative imaging revealed a severely displaced heart deep into the left chest. He was subsequently scheduled for coronary artery bypass grafting. However, altered anatomy from the absent pericardium required the procedure to be unexpectedly modified intraoperatively to address displaced coronary vessel targets that were surgically inaccessible. The patient's anterior vessels were grafted without complication, but the lateral and posterior vessels were unable to be grafted, due to excessive manipulation of the heart required for visualization. An intra-aortic balloon pump was utilized to maximize perfusion until a percutaneous coronary intervention could be completed by a cardiologist in these remaining vessels. CONCLUSIONS While congenital pericardial agenesis is a rare condition, the anatomic abnormalities encountered in this case are not uncommon within this patient population. These variances can interfere with standard coronary artery bypass grafting techniques. Understanding the unique challenges present in patients with this condition can aid in preoperative planning and coordination of a multispecialty approach for complicated revascularization.

先天性心包缺失混合型冠状动脉重建术一例报告。
背景:先天性心包发育不全是一种罕见的疾病,通常与胸内解剖结构异常有关,尤其是心脏在胸腔内的定位错位。在冠状动脉搭桥的情况下,这些解剖紊乱可能会给手术带来挑战,需要结合互补的非手术解决方案来实现完全的血运重建。病例报告一名48岁男性患者表现为急性心绞痛症状,检查显示严重的多支冠状动脉疾病,心包部分缺失。术前影像学显示一颗严重移位的心脏深入左胸。随后,他被安排进行冠状动脉旁路移植术。然而,由于心包缺失导致的解剖结构改变,需要术中对手术进行意外修改,以解决手术无法到达的移位冠状血管靶点。患者的前血管移植无并发症,但外侧和后血管无法移植,由于过度操作心脏需要可视化。使用主动脉内球囊泵使灌注最大化,直到心脏病专家对剩余血管进行经皮冠状动脉介入治疗。结论:虽然先天性心包发育不全是一种罕见的疾病,但本病例的解剖异常在该患者群体中并不罕见。这些差异会干扰标准的冠状动脉旁路移植术。了解这种情况下患者面临的独特挑战有助于术前规划和协调复杂血运重建术的多专业方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信