Cardiac Sarcoidosis Culminating in Severe Biventricular Failure
A 59-year-old woman with a history of lung sarcoidosis developed general edema and exertional dyspnea. An electrocardiogram showed first-degree atrioventricular block with complete right bundle branch block. Chest X-ray showed cardiomegaly. Echocardiography showed diffuse and severe hypokinesis of t...
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doaj-efe04b156a344af989536c007aa60ef52020-11-25T02:48:03ZengHindawi LimitedCase Reports in Medicine1687-96271687-96352009-01-01200910.1155/2009/856785856785Cardiac Sarcoidosis Culminating in Severe Biventricular FailureTakefumi Ozaki0Noritomo Ohnuma1Norihiro Shimizu2Atsushi Hasegawa3Masashi Horimoto4Division of Cardiovascular Disease, Chitose City Hospital, Chitose City, 066-8550, JapanDivision of Internal Medicine, Chitose City Hospital, Chitose City, 066-8550, JapanDivision of Cardiovascular Disease, Chitose City Hospital, Chitose City, 066-8550, JapanDivision of Internal Medicine, Chitose City Hospital, Chitose City, 066-8550, JapanDivision of Cardiovascular Disease, Chitose City Hospital, Chitose City, 066-8550, JapanA 59-year-old woman with a history of lung sarcoidosis developed general edema and exertional dyspnea. An electrocardiogram showed first-degree atrioventricular block with complete right bundle branch block. Chest X-ray showed cardiomegaly. Echocardiography showed diffuse and severe hypokinesis of the left ventricle (LV) and biventricular enlargement with severe tricuspid regurgitation. Myocardial scintigraphy disclosed a perfusion defect at the ventricular septum and hypoperfusion at the posterior wall and the apex. On cardiac catheterization, pulmonary capillary wedge pressure, right ventricular, and right atrial pressures were elevated. Coronary angiograms were normal. Myocardial biopsy of the right ventricle histologically revealed epithelioid cell granuloma with infiltration of fibrous cells. The patient's symptom and LV function were improved with conventional medical therapy for heart failure. This is a rare case of cardiac sarcoidosis resulting in biventricular failure.http://dx.doi.org/10.1155/2009/856785 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Takefumi Ozaki Noritomo Ohnuma Norihiro Shimizu Atsushi Hasegawa Masashi Horimoto |
spellingShingle |
Takefumi Ozaki Noritomo Ohnuma Norihiro Shimizu Atsushi Hasegawa Masashi Horimoto Cardiac Sarcoidosis Culminating in Severe Biventricular Failure Case Reports in Medicine |
author_facet |
Takefumi Ozaki Noritomo Ohnuma Norihiro Shimizu Atsushi Hasegawa Masashi Horimoto |
author_sort |
Takefumi Ozaki |
title |
Cardiac Sarcoidosis Culminating in Severe Biventricular Failure |
title_short |
Cardiac Sarcoidosis Culminating in Severe Biventricular Failure |
title_full |
Cardiac Sarcoidosis Culminating in Severe Biventricular Failure |
title_fullStr |
Cardiac Sarcoidosis Culminating in Severe Biventricular Failure |
title_full_unstemmed |
Cardiac Sarcoidosis Culminating in Severe Biventricular Failure |
title_sort |
cardiac sarcoidosis culminating in severe biventricular failure |
publisher |
Hindawi Limited |
series |
Case Reports in Medicine |
issn |
1687-9627 1687-9635 |
publishDate |
2009-01-01 |
description |
A 59-year-old woman with a history of lung sarcoidosis developed general edema and exertional dyspnea. An electrocardiogram showed first-degree atrioventricular block with complete right bundle branch block. Chest X-ray showed cardiomegaly. Echocardiography showed diffuse and severe hypokinesis of the left ventricle (LV) and biventricular enlargement with severe tricuspid regurgitation. Myocardial scintigraphy disclosed a perfusion defect at the ventricular septum and hypoperfusion at the posterior wall and the apex. On cardiac catheterization, pulmonary capillary wedge pressure, right ventricular, and right atrial pressures were elevated. Coronary angiograms were normal. Myocardial biopsy of the right ventricle histologically revealed epithelioid cell granuloma with infiltration of fibrous cells. The patient's symptom and LV function were improved with conventional medical therapy for heart failure. This is a rare case of cardiac sarcoidosis resulting in biventricular failure. |
url |
http://dx.doi.org/10.1155/2009/856785 |
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