Kearney Debra L
Baylor College of Medicine, Houston, TX, USA.
Semin Cardiothorac Vasc Anesth. 2013 Jun;17(2):105-16. doi: 10.1177/1089253213488247. Epub 2013 May 8.
Left-ventricular (LV) hypoplasia encompasses a range of LV sizes, varying from a mildly underdeveloped, but functionally adequate, chamber to the miniscule, barely perceptible LV cavity seen in hypoplastic left-heart syndrome. Associated malformations include obstructive lesions of LV inflow, outflow, and the aortic arch, often in combination. Repair of complex combinations and/or severe LV hypoplasia usually results in a single-ventricle anatomy with the right ventricle serving as the systemic ventricle. New therapeutic interventions, including fetal procedures, are expanding the spectrum of lesions and LV sizes that may be amenable to a biventricular repair. These surgical considerations place renewed emphasis on understanding the anatomical features associated with LV hypoplasia. This review details pathological features of the full spectrum of LV hypoplasia, particularly those with borderline severe hypoplasia. Primary defining lesions are described as well as additional lesions that may affect clinical symptoms, surgical repair, and long-term outcome.
左心室(LV)发育不全涵盖了一系列左心室大小情况,从轻度发育不良但功能尚充足的腔室到左心发育不全综合征中极小、几乎难以察觉的左心室腔。相关畸形包括左心室流入道、流出道及主动脉弓的梗阻性病变,且常合并存在。复杂组合畸形和/或严重左心室发育不全的修复通常会导致单心室解剖结构,右心室作为体循环心室。包括胎儿手术在内的新治疗干预措施正在扩大可能适合双心室修复的病变范围和左心室大小。这些手术考量再次强调了理解与左心室发育不全相关的解剖特征的重要性。本综述详细阐述了左心室发育不全全谱的病理特征,尤其是那些临界严重发育不全的特征。描述了主要的界定性病变以及可能影响临床症状、手术修复和长期预后的其他病变。