Suppr超能文献

一例通过多模态成像诊断的罕见免疫球蛋白G4相关性缩窄性心包炎病例

A Rare Case of Immunoglobulin G4-Related Constrictive Pericarditis Diagnosed Via Multimodality Imaging.

作者信息

Ozgur Sacide S, Tagliaferri Ariana, Aiken Arielle, Desai Binoy, Abboud Rachel, Shamoon Yezin, Akel Tamer, Singhal Monisha, Shamoon Fayez

机构信息

Department of Internal Medicine, St. Joseph's University Medical Center, Paterson, NJ, USA.

Department of Gastroenterology, Creighton University Medical Center, Phoenix, AZ, USA.

出版信息

J Investig Med High Impact Case Rep. 2024 Jan-Dec;12:23247096241248969. doi: 10.1177/23247096241248969.

Abstract

Constrictive pericarditis (CP) presents as a pathophysiological state where the pericardium becomes inelastic due to fibrotic changes, most commonly secondary to a protracted inflammatory process. The disease is characterized by compromised diastolic cardiac function due to loss of pericardial compliance. Immunoglobulin G4 (IgG4)-related disease, an entity marked by the insidious proliferation of IgG4-positive plasma cells and subsequent fibrosis within various organs, is an infrequent but recognized cause of CP. A case of a 55-year-old male patient with clinical manifestations of dyspnea and edema in the lower extremities elucidates the diagnostic complexity inherent to CP. Echocardiography revealed a constellation of signs, including annulus reversus, septal bounce, and a congested inferior vena cava; cardiac magnetic resonance imaging (MRI) demonstrated diffuse pericardial thickening with delayed gadolinium enhancement, suggestive of a long-term inflammatory state; and right heart catheterization confirmed the hemodynamic hallmark of CP-equalization of diastolic pressures across the cardiac chambers. The serological analysis elicited elevated serum levels of IgG4 and IgE, pointing to the differential diagnosis of IgG4-related disease. Given the nonspecific clinical presentation of IgG4-related CP, a heightened index of suspicion combined with a systematic approach to imaging and serological evaluation is paramount.

摘要

缩窄性心包炎(CP)表现为一种病理生理状态,即心包由于纤维化改变而变得缺乏弹性,最常见的是继发于长期的炎症过程。该疾病的特征是由于心包顺应性丧失导致舒张期心脏功能受损。免疫球蛋白G4(IgG4)相关疾病是一种以IgG4阳性浆细胞隐匿性增殖以及随后在各个器官内发生纤维化为特征的疾病,是CP的一种罕见但已被认识的病因。一名55岁男性患者出现呼吸困难和下肢水肿的临床表现,阐明了CP固有的诊断复杂性。超声心动图显示了一系列征象,包括瓣环反转、室间隔弹跳和下腔静脉淤血;心脏磁共振成像(MRI)显示弥漫性心包增厚并伴有钆延迟强化,提示长期炎症状态;右心导管检查证实了CP的血流动力学特征——心腔间舒张期压力均衡。血清学分析显示血清IgG4和IgE水平升高,提示IgG4相关疾病的鉴别诊断。鉴于IgG4相关CP的临床表现不具特异性,提高怀疑指数并结合系统的影像学和血清学评估方法至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c73f/11177727/4221c224475c/10.1177_23247096241248969-fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验