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1例罕见的伴有心包积液、传导异常及心房浸润的厄尔德海姆-切斯特病病例报告

A rare case report of Erdheim-Chester disease with pericardial effusion, conduction abnormalities, and atrial infiltration.

作者信息

Yassine Charaf, Colletti Giuseppe, Ciprian Acasandrei, George Mairesse

机构信息

Department of Cardiology, Saint-Joseph Clinic, Route de Lennik 808, Brussels, Belgium.

出版信息

Eur Heart J Case Rep. 2024 Jan 4;8(1):ytae002. doi: 10.1093/ehjcr/ytae002. eCollection 2024 Jan.

Abstract

BACKGROUND

Erdheim-Chester disease (ECD) is a rare multisystem disorder that primarily affects adults. It is characterized by the excessive production and accumulation of histiocytes, a type of white blood cell, within multiple tissues and organs, including the cardiovascular system. The infiltration of histiocytes can cause a range of cardiovascular symptoms, including pericardial effusion, myocardial infiltration, and heart failure, among others. Despite the potential severity of these cardiovascular manifestations, ECD is often misdiagnosed or underdiagnosed, leading to delays in appropriate treatment and poor outcomes for patients. As such, there is a pressing need for increased awareness and understanding of ECD's cardiovascular manifestations among clinicians and researchers. This article aims to highlight the importance of considering ECD as a potential underlying cause of cardiovascular complaints and to encourage further investigation into this uncommon but potentially life-threatening condition.

CASE SUMMARY

A 63-year-old man presented as outpatient complaining of dyspnoea on exertion during the last 3 weeks (New York Heart Association functional class III). He had also experienced a left shoulder and bilateral knee pain over the last 6 months. The patient was found to have a massive pericardial effusion associated with ECD. While pericardial effusions can have various causes, including infection, cancer, and autoimmune disorders, ECD is one potential cause of this condition. Therefore, it is important for clinicians to consider ECD in the differential diagnosis of patients presenting with unexplained pericardial effusions, particularly in the context of other systemic symptoms suggestive of ECD. We discuss about this specific aetiology and the clinical management of this uncommon condition.

DISCUSSION

Erdheim-Chester disease, a non-Langerhans cell histiocytosis, is a rare multisystem disorder. Diagnosis is challenging and should be suspected in the presence of a pericardial effusion with conduction abnormalities with indicators of a multisystem disease.

摘要

背景

厄尔德海姆-切斯特病(ECD)是一种罕见的多系统疾病,主要影响成年人。其特征是一种白细胞——组织细胞在包括心血管系统在内的多个组织和器官中过度产生和积聚。组织细胞的浸润可导致一系列心血管症状,包括心包积液、心肌浸润和心力衰竭等。尽管这些心血管表现可能很严重,但ECD常常被误诊或诊断不足,导致患者得不到及时恰当的治疗,预后不良。因此,临床医生和研究人员迫切需要提高对ECD心血管表现的认识和理解。本文旨在强调将ECD视为心血管疾病潜在病因的重要性,并鼓励对这种罕见但可能危及生命的疾病进行进一步研究。

病例摘要

一名63岁男性门诊就诊,主诉在过去3周内活动时呼吸困难(纽约心脏协会心功能分级III级)。他在过去6个月中还出现了左肩和双侧膝关节疼痛。该患者被发现患有与ECD相关的大量心包积液。虽然心包积液可能有多种原因,包括感染、癌症和自身免疫性疾病,但ECD是这种情况的一个潜在原因。因此,临床医生在对出现不明原因心包积液的患者进行鉴别诊断时,尤其是在存在提示ECD的其他全身症状的情况下,考虑ECD很重要。我们讨论了这种特定病因以及这种罕见疾病的临床管理。

讨论

厄尔德海姆-切斯特病是一种非朗格汉斯细胞组织细胞增多症,是一种罕见的多系统疾病。诊断具有挑战性,当出现心包积液并伴有传导异常以及多系统疾病指标时应怀疑该病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27d/10797487/0f1a077d7269/ytae002il2.jpg

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