Katz N M, Buckley M J, Liberthson R R
Circulation. 1977 Dec;56(6):1034-8. doi: 10.1161/01.cir.56.6.1034.
The presentation, management, and follow-up of 31 patients with discrete membranous subaortic stenosis (DMSS) is presented. DMSS comprised 16% of 185 patients with congenital left ventricular (LV) obstruction. Only one patient was older than 40 years. The rarity of DMSS in older patients in both our population and in the literature is noted, and possible explanations are discussed. One-quarter of these patients had dyspnea, chest pain, or syncope combined with electrocardiographic left ventricular hypertrophy (LVH) and strain, and these all had peak LV outflow gradients (PSG) greater than 85 mm Hg. One-quarter had neither symptoms nor electrocardiographic abnormalities and all had PSG less than 90 mm Hg. Bacterial endocarditis was found in 13%, and in 13% an immediate family member also had congenital LV obstruction. Following surgical resection (25 patients), 18 were asymptomatic, two had residual fibromuscular obstruction, and four developed new fibromuscular obstruction after from one to six years (leading in one to late sudden death). Thus, even after resection, these patients require continued re-evaluation for residual or new LV obstruction.
本文介绍了31例离散型膜性主动脉瓣下狭窄(DMSS)患者的临床表现、治疗及随访情况。DMSS占185例先天性左心室(LV)梗阻患者的16%。仅1例患者年龄超过40岁。注意到在我们的人群和文献中,老年患者中DMSS均很罕见,并讨论了可能的原因。这些患者中有四分之一出现呼吸困难、胸痛或晕厥,伴有心电图左心室肥厚(LVH)和劳损,且这些患者的左心室流出道峰值梯度(PSG)均大于85 mmHg。四分之一的患者既无症状也无心电图异常,且所有患者的PSG均小于90 mmHg。发现13%的患者患有细菌性心内膜炎,13%的患者直系亲属也患有先天性左心室梗阻。手术切除后(25例患者),18例无症状,2例有残余纤维肌性梗阻,4例在1至6年后出现新的纤维肌性梗阻(其中1例导致晚期猝死)。因此,即使在切除术后,这些患者仍需持续重新评估是否存在残余或新的左心室梗阻。