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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Main Authors: Takefumi Ozaki, Noritomo Ohnuma, Norihiro Shimizu, Atsushi Hasegawa, Masashi Horimoto
Format: Article
Language:English
Published: Hindawi Limited 2009-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2009/856785
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spelling 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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