SARS-CoV-2 感染是垂体中风的危险因素? 一个案例系列和文献综述
Christina Hazzi1, Noémie Villemure-Poliquin1, Sylvie Nadeau1
1Department of Ophthalmology and Otolaryngology-Head and Neck Surgery, CHU de Québec, Quebec, QC, Canada.
Ear, nose, & throat journal
|June 9, 2023
概括
垂体脑梗塞 (PA) 是一种罕见的垂体腺事件,越来越多地与COVID-19有关. 这项研究增加了三个病例,表明COVID-19可能直接导致PA,可能是由于凝血病,突出显示了一种新的临床关联.
科学领域:
- 内分泌学 在内分泌学.
- 神经学 神经学
- 传染性疾病 传染性疾病
背景情况:
- 垂体中风 (PA) 是一种罕见的内分泌紧急情况,涉及垂体腺出血或心脏病发作.
- 由SARS-CoV-2引起的COVID-19具有不同的临床表现.
- 已经注意到COVID-19感染和PA之间的新兴关联,但因果关系尚不清楚.
研究的目的:
- 报告与COVID-19和PA同时发生的患者的额外病例.
- 审查有关COVID-19相关的PA的现有文献.
- 讨论这种关联的潜在机制,治疗方法和结果.
主要方法:
- 从2020年3月到2021年12月,对PA和COVID-19患者的电子图表审查.
- 通过使用MEDLINE,Web of Science和Embase进行全面的文献搜索.
- 对临床表现,管理和结果的分析.
主要成果:
- 在症状性COVID-19感染后发现了三例新的PA病例.
- 由于持续的视力缺陷,两名患者需要手术干预.
- 文献审查发现了12个额外的病例,使报告的总数达到15.
- 在COVID-19感染后几天到两个月发生PA症状.
结论:
- 越来越多地认识到COVID-19和PA之间的关联,目前报告了15起病例.
- 凝血病是可能导致COVID-19患者垂体出血或心脏病发作的机制.
- 下垂体脑梗塞可能是COVID-19感染的直接表现.
更多相关视频
09:14Pre-Chiasmatic, Single Injection of Autologous Blood to Induce Experimental Subarachnoid Hemorrhage in a Rat Model
Published on: June 18, 2021
2.4K
10:21Author Spotlight: Exploring the Role of Inflammation in the Co-occurrence of Primary Sjogren's Syndrome and Lung Adenocarcinoma
Published on: September 20, 2024
498
相关概念视频
Aneurysm II: Clinical Manifestations and Diagnostic Studies
11
Thoracic, aortic arch and abdominal aneurysms are significant vascular conditions that can present with various clinical manifestations and lead to serious complications. Understanding these manifestations and the appropriate diagnostic studies is essential for effective management and treatment.Thoracic Aortic AneurysmsThoracic aortic aneurysms often remain asymptomatic until they reach a size that impinges on adjacent structures. They typically cause deep, diffuse chest pain that radiates to...
11
Single Nucleotide Polymorphisms-SNPs
15.3K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.3K
