心脏结节病与特发性扩张型心肌病的临床特征及预后比较。
Comparison of clinical features and prognosis of cardiac sarcoidosis and idiopathic dilated cardiomyopathy.
作者信息
Yazaki Y, Isobe M, Hiramitsu S, Morimoto S, Hiroe M, Omichi C, Nakano T, Saeki M, Izumi T, Sekiguchi M
机构信息
First Department of Internal Medicine, Shinshu University, Matsumoto, Japan.
出版信息
Am J Cardiol. 1998 Aug 15;82(4):537-40. doi: 10.1016/s0002-9149(98)00377-4.
In the present study, clinical findings of 15 patients with cardiac sarcoidosis presenting as dilated cardiomyopathy were compared with those of 30 consecutive patients with idiopathic dilated cardiomyopathy. The sarcoidosis patients had different clinical features, including female predominance, a high incidence of grave conduction disturbance and abnormal wall thickness, uneven wall motion abnormalities, and perfusion defects preferentially affecting the anteroseptal and apical regions, and poor prognosis compared with those with idiopathic dilated cardiomyopathy.
在本研究中，将15例表现为扩张型心肌病的心脏结节病患者的临床特征与30例连续的特发性扩张型心肌病患者的临床特征进行了比较。结节病患者具有不同的临床特征，包括女性占多数、严重传导障碍和异常壁厚的发生率高、壁运动异常不均匀、灌注缺损优先影响前间隔和心尖区域，以及与特发性扩张型心肌病患者相比预后较差。
Zotero 插件