Recurrent prosthetic mitral valve thrombosis: First report of an unusual feature of systemic mastocytosis, a case report and review of the literature.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Caspian Journal of Internal Medicine Pub Date : 2024-10-27 eCollection Date: 2025-01-01 DOI:10.22088/cjim.16.1.178
Amirhossein Akbarzadehpasha, Zahra Lotfi, Razieh Omidvar, Azadeh Goodarzi, Saeid Hosseini, Afsaneh Sadeghzadeh Bazargan, Kambiz Kamyab Hesari
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Abstract

Background: Mastocytosis is a systemic disease involving the clonal expansion of mast cells in multiple organs. Given that immune system overreaction and excessive histamine release are among the most prominent events in mastocytosis, the incidence of complications caused by immune reactions is expected to increase across various organs. While systemic manifestations of mastocytosis have been reported frequently, cardiac complications are less often discussed. These Cardiac complications can be early indicators of the disease but such uncommon features may lead to delays in diagnosis.The significance of mast cells and histamine release in the cardiovascular system is acknowledged in prior studies.

Case presentation: This study presents a case of recurrent prosthetic mitral valve malfunction in a 52-year-old patient with a history of cutaneous mastocytosis, who underwent mitral valve replacement three times over ten years. Despite being on appropriate anticoagulation therapy (INR: 2.5-3.5), the patient experienced recurrent prosthetic valve thrombosis. This is, to our knowledge, the first report of prosthetic mitral valve thrombosis in a patient with mastocytosis.

Conclusion: Interestingly, cardiac complications may be the first presentation of systemic mastocytosis, diagnosed long after the initial symptoms. The majority of such cases had no visible cutaneous manifestations (table 1). Regarding our case report, we recommend our colleagues to closely monitor and remain vigilant for possible cardiac symptoms of mastocytosis patients with prosthetic cardiac valves.

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复发性人工二尖瓣血栓形成:首次报道系统性肥大细胞增多症的不寻常特征,一例报告和文献回顾。
背景:肥大细胞增多症是一种涉及多器官肥大细胞克隆扩增的全身性疾病。鉴于免疫系统的过度反应和过量的组胺释放是肥大细胞增多症中最突出的事件之一,免疫反应引起的并发症的发生率预计会在各个器官中增加。虽然肥大细胞增多症的全身性表现经常被报道,但心脏并发症却很少被讨论。这些心脏并发症可能是疾病的早期指标,但这些不常见的特征可能导致诊断延误。肥大细胞和组胺释放在心血管系统中的重要性在先前的研究中得到承认。病例介绍:本研究报告了一例52岁的皮肤肥大细胞增多症患者复发性二尖瓣功能障碍,他在十年内接受了三次二尖瓣置换术。尽管接受了适当的抗凝治疗(INR: 2.5-3.5),患者仍复发了人工瓣膜血栓形成。这是,据我们所知,第一个报告假二尖瓣血栓患者肥大细胞增多症。结论:有趣的是,心脏并发症可能是全身性肥大细胞增多症的第一个表现,在最初症状出现很久之后才被诊断出来。这些病例大多数没有明显的皮肤表现(表1)。对于我们的病例报告,我们建议我们的同事密切监测和警惕肥大细胞增多症患者植入假心脏瓣膜后可能出现的心脏症状。
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来源期刊
Caspian Journal of Internal Medicine
Caspian Journal of Internal Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
1.90
自引率
7.10%
发文量
90
审稿时长
20 weeks
期刊最新文献
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