心内膜纤维细胞增生症:发病机制、临床表现、诊断方式和管理策略的全面回顾

Donaldo Emiliano Silva López, Oyuky Yumary Citlalli Flores Alamos, Saúl Villaseñor Angulo, Diana Marisol Perales Rivera, Verónica Guadalupe Vázquez Rubio, Domingo Antonio Manriquez Vazquez
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引用次数: 0

摘要

心内膜纤维细胞增生症(EFE)是一种罕见而神秘的心肌疾病,其特征是心内膜胶原纤维和弹性纤维的异常堆积,主要影响左心室。本综述旨在阐明 EFE 的发病机制、临床表现、诊断方法和治疗策略。EFE 通常发生在婴幼儿身上,但也有成人病例的报道。EFE 的病因仍然难以捉摸,理论上与遗传、感染和自身免疫因素有关。临床上,EFE 可能表现为心力衰竭、心律失常或心脏性猝死症状。诊断通常需要超声心动图、心脏磁共振成像和心内膜活检。EFE 的治疗策略主要是支持性治疗,重点是控制心衰症状和心律失常,晚期病例则需要进行心脏移植。本综述全面概述了 EFE,强调了诊断和管理方面的挑战,并强调了进一步研究以阐明其发病机制和改善预后的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endocardial Fibroelastosis: A Comprehensive Review of Pathogenesis, Clinical Manifestations, Diagnostic Modalities, and Management Strategies
Endocardial fibroelastosis (EFE) is a rare and enigmatic myocardial disease characterized by the abnormal accumulation of collagen and elastin fibers in the endocardium, predominantly affecting the left ventricle. This comprehensive review aims to elucidate the pathogenesis, clinical manifestations, diagnostic modalities, and management strategies of EFE. EFE typically presents in infants and young children, although adult cases have been reported. The etiology of EFE remains elusive, with theories implicating genetic, infectious, and autoimmune factors. Clinically, EFE may manifest with symptoms of heart failure, arrhythmias, or sudden cardiac death. Diagnosis often involves echocardiography, cardiac magnetic resonance imaging, and endomyocardial biopsy. Management strategies for EFE are primarily supportive, focusing on the management of heart failure symptoms and arrhythmias, with advanced cases necessitating heart transplantation. This review provides a comprehensive overview of EFE, highlighting the challenges in diagnosis and management and underscoring the need for further research to elucidate its pathogenesis and improve outcomes.
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