罗赛-多夫曼病的心脏表现:病例报告与系统回顾

IF 0.7 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Nika Samadzadeh Tabrizi, Muhammad Hassan Dogar, Daniel Wilkinson, Perry Stout, Siyamek Neragi-Miandoab, Sanjay Samy
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引用次数: 0

摘要

背景介绍罗赛-多夫曼病是一种罕见病,通常表现为结节病。心脏受累极为罕见,仅占病例的 0.1-0.2%,这阻碍了我们对该病的了解。我们报告了一例罗赛-多夫曼病(RDD)相关的心脏表现病例,患者没有结节受累。此外,我们还对文献进行了全面回顾,以整合有关 RDD 心脏表现患者通常如何处理和治疗的数据:方法:我们对 PubMed、Web of Science 和 Embase 进行了系统回顾,以确定心脏受累的 RDD 病例。在已确定的 464 项研究中,有 42 篇包含 43 名患者的文献符合标准,并被纳入本综述。我们收集了有关患者人口统计学、管理和治疗方法的数据。此外,我们还分享了一位因 RDD 而出现心脏肿块的患者的亲身经历:在 43 名患者中,仅有 20.9% 的患者(n = 9)在出现心脏表现前有 RDD 病史记录。结节受累占 32.6%(14 例),结节外心脏外受累占 46.5%(20 例)。发病时最常见的症状是呼吸困难(48.8%,n = 21)、胸部不适(41.9%,n = 18)和下肢水肿(16.3%,n = 7)。心脏表现最常见于右心房(41.9%,18 人)和心包(18.6%,8 人)。治疗包括全身药物治疗(34.9%,n = 15)和心脏手术(39.5%,n = 17)。中位随访时间为 12 个月(1 到 36 个月),8 名患者(18.6%)死亡。我们的患者左心房有心脏肿块,接受了切除手术,在过去的 5 年中一直没有症状,也没有复发:结论:与心脏相关的 RDD 表现的发生率可能比最初认为的要高。这些结果强调了识别 RDD 及其心脏相关表现的重要性,有助于对患者进行及时诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiac Manifestation of Rosai-Dorfman Disease: A Case Report and a Systematic Review.

Background: Rosai-Dorfman disease is a rare condition that typically presents as a nodal disease. Cardiac involvement is extremely uncommon, occurring in 0.1-0.2% of cases, which has hindered our understanding. We report a case of Rosai-Dorfman disease (RDD) related cardiac manifestation in a patient without nodal involvement. Further, we conduct a comprehensive review of the literature to consolidate data on how patients with cardiac manifestations of RDD are typically managed and treated.

Methods: A systematic review of PubMed, Web of Science, and Embase was conducted to identify cases of RDD with cardiac involvement. Out of 464 studies identified, 42 publications encompassing 43 patients met the criteria and were incorporated in this review. We gathered data on patient demographics, as well as their management and treatment approaches. Additionally, we share our own experience with a patient who presented with a cardiac mass related to RDD.

Results: Out of the 43 patients, only 20.9% (n = 9) had a documented history of RDD prior to cardiac manifestations. Nodal involvement was reported in 32.6% (n = 14), while extranodal extracardiac involvement was reported in 46.5% (n = 20). Upon presentation, the most prevalent symptoms were dyspnea (48.8%, n = 21), chest discomfort (41.9%, n = 18), and lower extremity edema (16.3%, n = 7). Cardiac manifestations were most frequently found in the right atrium (41.9%, n = 18) and pericardium (18.6%, n = 8). Treatment encompassed systemic medical therapy (34.9%, n = 15) and cardiac surgery (39.5%, n = 17). The median follow-up period was 12 months (with a range of 1 to 36), and 8 patients (18.6%) experienced mortality. Our patient, who had a cardiac mass in the left atrium, underwent resection and has remained symptom-free without any recurrence for the past 5 years.

Conclusion: The frequency of cardiac related-RDD manifestations may be greater than initially perceived. These results underscore the significance of identifying RDD and its cardiac-related presentations, facilitating timely diagnosis and treatment for affected individuals.

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来源期刊
Heart Surgery Forum
Heart Surgery Forum 医学-外科
CiteScore
1.20
自引率
16.70%
发文量
130
审稿时长
6-12 weeks
期刊介绍: The Heart Surgery Forum® is an international peer-reviewed, open access journal seeking original investigative and clinical work on any subject germane to the science or practice of modern cardiac care. The HSF publishes original scientific reports, collective reviews, case reports, editorials, and letters to the editor. New manuscripts are reviewed by reviewers for originality, content, relevancy and adherence to scientific principles in a double-blind process. The HSF features a streamlined submission and peer review process with an anticipated completion time of 30 to 60 days from the date of receipt of the original manuscript. Authors are encouraged to submit full color images and video that will be included in the web version of the journal at no charge.
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