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双重挑战:家族性胸主动脉瘤患者的心内膜炎——病例报告及文献综述

A Dual Challenge: Endocarditis in a Patient with Familial Thoracic Aortic Aneurysm-Case Report and Literature Review.

作者信息

Cozlac Alina-Ramona, Streian Caius Glad, Boca Marciana Ionela, Crisan Simina, Lazar Mihai-Andrei, Virtosu Mirela-Daniela, Ionac Adina, Staicu Raluca Elisabeta, Dugaci Daniela-Carmen, Emandi-Chirita Adela, Lascu Ana, Gaita Dan, Luca Constantin-Tudor

机构信息

Department VI Cardiology-Cardiovascular Surgery, "Victor Babes" University of Medicine and Pharmacy of Timișoara, Eftimie Murgu Square No. 2, 300041 Timisoara, Romania.

Institute for Cardiovascular Diseases of Timisoara, "Victor Babes" University of Medicine and Pharmacy of Timisoara, G. Adam Str. No. 13A, 300310 Timisoara, Romania.

出版信息

J Clin Med. 2024 Nov 26;13(23):7155. doi: 10.3390/jcm13237155.

Abstract

: Thoracic aortic aneurysms (TAAs) are potentially life-threatening medical conditions, and their etiology involves both genetic and multiple risk factors. endocarditis is one of the most frequent causes of blood culture-negative infective endocarditis (BCNIE) in patients with previous cardiac surgery. Our review aims to emphasize the importance of genetic testing in patients with thoracic aortic aneurysms but also the importance of additional testing in patients with suspected endocarditis whose blood cultures remain negative. The reported case has a history of acute DeBakey type I aortic dissection that developed during her second pregnancy, for which the Bentall procedure was performed at that time. Ten years after the surgery, the patient started developing prolonged febrile syndrome with repeatedly negative blood cultures, the serological tests revealing the presence of an infection with . Considering her family history and the onset of her aortic pathology at a young age, genetic tests were performed, disclosing a missense variant in the actin alpha-2 () gene in heterozygous status. : For a better understanding of both conditions, our research was conducted in two directions: one reviewing the literature on patients with BCNIE and the other focusing on patients who had a familial thoracic aortic aneurysm (FTAA) due to the variant. This review incorporates studies found on PubMed and ResearchGate up to August 2024. : BCNIE represents a condition with several diagnostic challenges and may lead to severe complications if timely treatment is not initiated. Also, diagnosing an FTAA requires genetic testing, enabling better follow-up and management.

摘要

胸主动脉瘤(TAAs)是具有潜在生命威胁的病症,其病因涉及遗传因素和多种风险因素。心内膜炎是既往有心脏手术史患者血培养阴性感染性心内膜炎(BCNIE)最常见的病因之一。我们的综述旨在强调胸主动脉瘤患者基因检测的重要性,同时也强调对血培养持续阴性的疑似心内膜炎患者进行额外检测的重要性。报告的病例有急性DeBakey I型主动脉夹层病史,在其第二次怀孕期间发病,当时进行了Bentall手术。手术后十年,患者开始出现持续发热综合征,血培养反复阴性,血清学检测显示存在感染。考虑到她的家族病史以及主动脉病变在年轻时发病,进行了基因检测,发现肌动蛋白α-2()基因存在杂合状态的错义变异。:为了更好地理解这两种病症,我们的研究从两个方向进行:一个方向是回顾关于BCNIE患者的文献,另一个方向是关注因该变异而患有家族性胸主动脉瘤(FTAA)的患者。本综述纳入了截至2024年8月在PubMed和ResearchGate上找到的研究。:BCNIE是一种具有多种诊断挑战的病症,如果不及时治疗可能会导致严重并发症。此外,诊断FTAA需要基因检测,以便更好地进行随访和管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7cf/11642186/82992ec01935/jcm-13-07155-g001.jpg

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