Kiyooka Takahiko, Satoh Yasuhiro
Division of Cardiology, Tokai University Oiso Hospital, 21-1 Gakkyo, Oisomachi, Nakagun, Kanagawa 259-0198, Japan.
Tokai J Exp Clin Med. 2014 Mar 20;39(1):29-33.
Mid-ventricular obstructive hypertrophic cardiomyopathy (MVOHCM) is a rare form of cardiomyopathy, characterized by the presence of a pressure gradient between the left ventricular basal and apical chambers and is frequently associated with an apical aneurysm. However, the exact cause of this aneurysm remains unknown. We here describe a patient with MVOHCM in whom the apical aneurysm may be caused by vasospastic angina.
心室中部梗阻性肥厚型心肌病（MVOHCM）是一种罕见的心肌病形式，其特征是左心室基部和心尖部腔室之间存在压力梯度，且常伴有心尖部动脉瘤。然而，这种动脉瘤的确切病因尚不清楚。我们在此描述一名MVOHCM患者，其心尖部动脉瘤可能由血管痉挛性心绞痛引起。
