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皮质类固醇治疗后特发性巨细胞心肌炎所致完全性房室传导阻滞的恢复情况。

Recovery from complete atrioventricular block caused by idiopathic giant cell myocarditis after corticosteroid therapy.

作者信息

Hanawa H, Izumi T, Saito Y, Ochiai Y, Okura Y, Inomata T, Hirono S, Ogawa Y, Saito R, Kodama M, Higuma N, Aizawa Y

机构信息

First Department of Internal Medicine, Niigata University School of Medicine, Asahimachi, Japan.

出版信息

Jpn Circ J. 1998 Mar;62(3):211-4. doi: 10.1253/jcj.62.211.

Abstract

Giant cell myocarditis (GCM) is a rapidly progressive disease that leads to ventricular tachycardia or high-grade atrioventricular (A-V) block, frequently requiring a pacemaker. A 64-year-old woman developed syncope as a result of idiopathic GCM with A-V block. She required both a temporary and a permanent pacemaker. Two-dimensional echocardiography showed severely reduced wall motion. There was no histologic or clinical evidence to suggest sarcoidosis. Despite treatment with diuretics and an angiotensin-converting enzyme inhibitor, exertional dyspnea persisted. She received prednisolone 4 months after the onset of complete A-V block in the late phase of GCM. Prednisolone improved A-V nodal conduction in spite of the fact that there was no influence from LV wall motion, and sinus rhythm has continued for more than 2 years. In this patient, prednisolone was effective in the treatment of GCM.

摘要

巨细胞性心肌炎(GCM)是一种快速进展的疾病,可导致室性心动过速或高度房室传导阻滞,常常需要安装起搏器。一名64岁女性因特发性GCM伴房室传导阻滞而出现晕厥。她既需要临时起搏器也需要永久起搏器。二维超声心动图显示室壁运动严重减弱。没有组织学或临床证据提示结节病。尽管使用了利尿剂和血管紧张素转换酶抑制剂治疗,劳力性呼吸困难仍持续存在。在GCM晚期完全性房室传导阻滞发生4个月后,她开始接受泼尼松龙治疗。尽管左心室壁运动没有受到影响,但泼尼松龙改善了房室结传导,窦性心律已持续超过2年。在该患者中,泼尼松龙对GCM治疗有效。

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