van Hoeven K H, Kitsis R N, Katz S D, Factor S M
Department of Pathology, Albert Einstein College of Medicine, Bronx, NY.
Int J Cardiol. 1993 Jun 15;40(1):57-65. doi: 10.1016/0167-5273(93)90231-5.
Clinicopathologic features of 13 women with peripartum cardiomyopathy were compared to 13 women aged 19 through 38 with idiopathic dilated cardiomyopathy. No presenting clinical or pathologic variable distinguished either group. However, the clinical course differed between the groups. Eleven of 13 patients with idiopathic dilated cardiomyopathy had a poor clinical outcome, defined as persistent heart failure or death. Patients in this group succumbed one year or more after disease onset. Five of 13 patients with peripartum cardiomyopathy had poor outcome, with death occurring 9 months or less after disease onset. The clinical course of peripartum cardiomyopathy appears distinct from that of idiopathic dilated cardiomyopathy in young women.
将13例围产期心肌病女性患者的临床病理特征与13例年龄在19至38岁之间的特发性扩张型心肌病女性患者进行了比较。两组在临床表现或病理变量上均无差异。然而,两组的临床病程有所不同。13例特发性扩张型心肌病患者中有11例临床预后较差,定义为持续性心力衰竭或死亡。该组患者在疾病发作一年或更长时间后死亡。13例围产期心肌病患者中有5例预后较差,在疾病发作后9个月或更短时间内死亡。围产期心肌病的临床病程似乎与年轻女性特发性扩张型心肌病不同。