DSpace About DSpace Software 日本語
 

GINMU >
01 奈良県立医科大学 >
011 医学部 >
0112 紀要 >
01121 Journal of Nara Medical Association >
Vol.45 No.4 >

Please use this identifier to cite or link to this item: http://hdl.handle.net/10564/1639

Title: 特発性拘束型心筋症の1症例
Other Titles: A CASE OF IDIOPATHIC RESTRICTIVE CARDIOMYOPATHY
Authors: 酢谷, 俊夫
坂口, 泰弘
赤井, 真弓
橋本, 俊雄
籠島, 忠
土肥, 和紘
Keywords: congestive heart failure
dip and plateau
idiopathic restrictive cardiomyopathy
myocardial biopsy
Issue Date: 31-Aug-1994
Publisher: 奈良医学会
Citation: 奈良医学雑誌 Vol.45 No.4 p.353-359
Abstract: Most cases of restrictive cardiomyopathy (RCM) are caused by cardiac amyloidosis, cardiac hemochromatosis and endocardial fibrosis as the sequela of tropical or nontropical hypereosinophilia or endocardial fibroelastosis. We present herein a case of idiopathic RCM diagnosed by echocardiogram, cardiac catheterization and myocardial biopsy. This patient was a 33-year-old woman. She had been suffering from dyspnea on effort, abdominal fullness and pretibial edema. Persistent atrial fibrillation was seen on electrocardiogram and increase of cardiotrachic ratio (58.6%) on chest X-ray was seen on admission. Echocardiogram revealed a decrease of left ventricular diastolic properties with no decrease of left ventricular ejction fraction. Cardiac catheterization revealed an early diastolic dip and plateau pattern and increased end-diastolic pressure of both ventricles. A myocardial biopsy from the right ventricular wall disclosed mild hypertrophy of myocytes, interstitial fibrosis and endocardial thickening without the deposition of amyloid and hemosiderin.
URI: http://hdl.handle.net/10564/1639
ISSN: 04695550
13450069
Appears in Collections:Vol.45 No.4

Files in This Item:

File Description SizeFormat
353-359p:特発性拘束型心筋症の1症例.pdf958.97 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

Valid XHTML 1.0! DSpace Software Copyright © 2002-2010  Duraspace - Feedback