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左心室致密化不全。

Left ventricular hypertrabeculation/noncompaction.

作者信息

Stöllberger Claudia, Finsterer Josef

机构信息

Krankenanstalt Rudolfstiftung, 2. Med. Abteilung, Vienna, Austria.

出版信息

J Am Soc Echocardiogr. 2004 Jan;17(1):91-100. doi: 10.1016/S0894-7317(03)00514-5.

Abstract

In normal human hearts the left ventricle (LV) has up to 3 prominent trabeculations and is, thus, less trabeculated than the right ventricle. Rarely, more than 3 prominent trabeculations can be found at autopsy and by various imaging techniques in the LV. For this abnormality, different synonyms are used such as spongy myocardium, LV noncompaction, and LV hypertrabeculation (LVHT). In this review it is stated that: (1) LVHT has a higher prevalence than previously thought and the prevalence of LVHT seems to increase with the improvement of cardiac imaging; (2) because LVHT is most frequently diagnosed primarily by echocardiography, echocardiographers should be aware and trained to recognize this abnormality; (3) LVHT is frequently associated with other cardiac and extracardiac, particularly neuromuscular, disorders; (4) there are indications that the cause of LVHT is usually a genetic one and quite heterogeneous; and (5) controversies exist about diagnostic criteria, nomenclature, prognosis, origin, pathogenesis, and the necessity to classify LVHT as a distinct entity and cardiomyopathy by the World Health Organization.

摘要

在正常人体心脏中,左心室(LV)有多达3个明显的肌小梁,因此其肌小梁比右心室少。在尸检以及通过各种成像技术检查左心室时,很少能发现超过3个明显的肌小梁。对于这种异常情况,使用了不同的同义词,如海绵状心肌、左心室心肌致密化不全和左心室肌小梁增多(LVHT)。本综述指出:(1)LVHT的患病率高于先前认为的,且随着心脏成像技术的改进,LVHT的患病率似乎有所增加;(2)由于LVHT最常主要通过超声心动图诊断,超声心动图检查人员应意识到并接受培训以识别这种异常;(3)LVHT常与其他心脏和心脏外疾病相关,尤其是神经肌肉疾病;(4)有迹象表明,LVHT的病因通常是遗传性的,且相当异质;(5)关于诊断标准、命名、预后、起源、发病机制以及世界卫生组织将LVHT归类为一种独特实体和心肌病的必要性存在争议。

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