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Sarcoid heart disease

Identifieur interne : 001B04 ( Main/Exploration ); précédent : 001B03; suivant : 001B05

Sarcoid heart disease

Auteurs : Simon W. Dubrey [Royaume-Uni] ; Alex Bell [Royaume-Uni] ; Tarun K. Mittal

Source :

Postgraduate Medical Journal [ 0032-5473 ] ; 2007-10.

RBID : ISTEX:8156C60FB7BEAC34A28DCADC41DC275A0D03EA8D

English descriptors

Teeft :
- Abnormal wall motion, Abnormality, Alex bell, Biopsy, Black patients, British thoracic, Cardiac, Cardiac involvement, Cardiac sarcoidosis, Cardiac transplantation, Cardiomyopathy, Cardiovasc drugs, Cell activation, Chest radiographs, Clin chest, Clinical course, Coronary artery disease, Curr opin pulm, Dysfunction, Echocardiographic appearances, Endomyocardial, Endomyocardial biopsy, Enhancement, Erythema nodosum, Focal areas, Granuloma, Granulomatous inflammation, Harefield hospital, Heart block, Heart failure, Heart involvement, Heart transplantation, High resolution, Hilar lymphadenopathy, Hillingdon hospital, Imaging, Imaging techniques, Interventricular septum, Kveim test, Lymph nodes, Lymphadenopathy, Magnetic resonance imaging, Many cases, Many patients, Myocardial, Myocardial involvement, Myocardial sarcoidosis, Myocardial scintigraphy, Neurologic dysfunction, Node, Organ involvement, Other granulomatous diseases, Personal communication, Positron emission tomography, Primary cause, Pulmonary involvement, Pulmonary sarcoid, Pulmonary sarcoidosis, Restrictive cardiomyopathy, Sarcoid, Sarcoid granulomas, Sarcoid heart disease, Sarcoidosis, Scintigraphy, Septum, Short axis, Soft tissue resolution, Therapeutic considerations, Transplant, Transplant data, Transplantation, Tuberculosis association, Ventricular, Ventricular aneurysm formation, Weighted images.

Abstract

To this day the aetiology of sarcoidosis continues to elude definition. Partially as a consequence of this, little in the way of new therapies has evolved. The enigma of this condition is that, unusually for a disease with the potential for devastating consequences, many patients show spontaneous resolution and recover. Cardiac involvement can affect individuals of any age, gender or race and has a predilection for the conduction system of the heart. Heart involvement can also cause a dilated cardiomyopathy with consequent progressive heart failure. The most common presentation of this systemic disease is with pulmonary infiltration, but many cases will be asymptomatic and are detected on routine chest radiography revealing lymphadenopathy. Current advances lie in the newer methods of imaging and diagnosing this unusual heart disease. This review describes the pathology and diagnosis of this condition and the newer imaging techniques that have developed for determining cardiac involvement.

Url:

https://api.istex.fr/ark:/67375/NVC-CB0MP8P3-W/fulltext.pdf

DOI: 10.1136/pgmj.2007.060608

Affiliations:

Royaume-Uni

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Le document en format XML

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<term>British thoracic</term>
<term>Cardiac</term>
<term>Cardiac involvement</term>
<term>Cardiac sarcoidosis</term>
<term>Cardiac transplantation</term>
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<term>Cardiovasc drugs</term>
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<term>Clinical course</term>
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<term>Curr opin pulm</term>
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<term>Granulomatous inflammation</term>
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<term>Heart block</term>
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<term>Heart involvement</term>
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<term>Many patients</term>
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<term>Organ involvement</term>
<term>Other granulomatous diseases</term>
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<term>Soft tissue resolution</term>
<term>Therapeutic considerations</term>
<term>Transplant</term>
<term>Transplant data</term>
<term>Transplantation</term>
<term>Tuberculosis association</term>
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<front><div type="abstract" xml:lang="en">To this day the aetiology of sarcoidosis continues to elude definition. Partially as a consequence of this, little in the way of new therapies has evolved. The enigma of this condition is that, unusually for a disease with the potential for devastating consequences, many patients show spontaneous resolution and recover. Cardiac involvement can affect individuals of any age, gender or race and has a predilection for the conduction system of the heart. Heart involvement can also cause a dilated cardiomyopathy with consequent progressive heart failure. The most common presentation of this systemic disease is with pulmonary infiltration, but many cases will be asymptomatic and are detected on routine chest radiography revealing lymphadenopathy. Current advances lie in the newer methods of imaging and diagnosing this unusual heart disease. This review describes the pathology and diagnosis of this condition and the newer imaging techniques that have developed for determining cardiac involvement.</div>
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Sarcoid heart disease

Sarcoid heart disease

Source :

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri