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Severe Austrian Syndrome in an Immunocompromised Adult Patient - A Case Report.

Authors :
Chirteș IR
Florea D
Chiriac C
Mărginean OM
Mănășturean C
Vitin AA
Georgescu AM
Source :
Journal of critical care medicine (Universitatea de Medicina si Farmacie din Targu-Mures) [J Crit Care Med (Targu Mures)] 2018 Feb 09; Vol. 4 (1), pp. 17-22. Date of Electronic Publication: 2018 Feb 09 (Print Publication: 2018).
Publication Year :
2018

Abstract

Background: Known also as Osler's triad, Austrian syndrome is a complex pathology which consists of pneumonia, meningitis and endocarditis, all caused by the haematogenous dissemination of Streptococcus pneumoniae. The multivalvular lesions are responsible for a severe and potential lethal outcome.<br />Case Report: The case of a 51-year-old female patient, with a past medical history of splenectomy, is presented. She developed bronchopneumonia, acute meningitis and infective endocarditis as a result of Streptococcus pneumoniae infection and subsequently developed multiple organ dysfunction syndromes which led to a fatal outcome. Bacteriological tests did not reveal the etiological agent. The histopathological examination showed a severe multivalvular endocarditis, while a PCR based molecular analysis from formalin fixed valvular tissue identified Streptococcus pneumoniae as the etiologic agent.<br />Conclusions: The presented case shows a rare syndrome with a high risk of morbidity and mortality. Following the broad-spectrum treatment and intensive therapeutic support, the patient made unfavourable progress which raised differential diagnosis problems. In this case, the post-mortem diagnosis demonstrated multiple valvular lesions occurred as a result of endocarditis.<br />Competing Interests: Conflict of interest: None to declare.

Details

Language :
English
ISSN :
2393-1809
Volume :
4
Issue :
1
Database :
MEDLINE
Journal :
Journal of critical care medicine (Universitatea de Medicina si Farmacie din Targu-Mures)
Publication Type :
Academic Journal
Accession number :
29967896
Full Text :
https://doi.org/10.1515/jccm-2017-0025