A case of endocarditis parietalis fibroplastica (Löffler's disease) is described and the aetiology and pathogenesis briefly discussed. Some of the relevant literature is reviewed.
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http://dx.doi.org/10.1136/pgmj.44.509.251 | DOI Listing |
Clin Res Cardiol
October 2019
Klinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Liebigstraße 20, 04103, Leipzig, Germany.
J Fish Dis
May 2018
Clinic for Birds, Reptiles, Amphibians and Fish, Justus Liebig University, Giessen, Germany.
Since the 1940s, the anadromous allis shad, Alosa alosa (L.), has suffered population declines throughout its distribution range in Europe. In context of EU-LIFE projects for the reintroduction of the allis shad in the Rhine system, a comprehensive study was started in 2012 to investigate infectious diseases occurring in allis shad.
View Article and Find Full Text PDFBMC Cardiovasc Disord
March 2017
Department of Cardiology, Pulmonology and Vascular Medicine, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany.
Background: Endocarditis parietalis fibroplastica Löfflein (EPF) is a rare form of primary restrictive cardiomyopathy with poor prognosis. It is generally caused by hypereosinophilic syndrome with eosinophilic penetration of the heart. This leads to congestive heart failure in three different stages.
View Article and Find Full Text PDFHistopathology
January 2005
Institute of Pathology, University Hospital of Essen, Essen, Germany.
Aims: Eosinophilic heart syndromes are rare in Western countries and include endocarditis parietalis fibroplastica (EPF) and hypersensitivity myocarditis (HM). There are striking differences in natural history and morphological findings. Since diagnosis can be difficult when analysing small myocardial biopsies lacking the characteristic histological features, we studied a set of immunohistochemical markers in order to characterize the activation status of the infiltrating eosinophils to distinguish between these two entities.
View Article and Find Full Text PDFMed Klin (Munich)
March 2000
Medizinische Klinik II mit Poliklinik, Friedrich-Alexander-Universität Erlangen-Nürnberg.
Case Report: The case of a 57-year-old woman is reported who was admitted for peripheral hypereosinophilia.
Diagnosis: Detailed investigations revealed first of all a hypereosinophilic syndrome with infiltration of bone marrow and lung. The patient suffered more and more from angina pectoris with signs of heart failure.
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