Clinical vignette
Primary mural endocarditis
Peadar F. McKeown1*, Patrick M. Donnelly2, and Daniel J. Flannery1
1Cardiology Department, Craigavon Area Hospital, 68 Lurgan Road, Portadown, BT63 5QQ, UK and 2Belfast City Hospital, 51 Lisburn Road, Belfast, BT9 7AB, UK
*Corresponding author. Tel: +44 2838334444; fax: +44 2838394802. E-mail address: peadar.mckeown@ntlworld.com
A 57-year-old male was admitted with a 2-week history of fever, rigours, and confusion and a single episode of retrosternal chest pain. He had recently undergone a circumcision. Clinical examination revealed a temperature of 38.3°C and a balanitis. Urinanalysis revealed haematuria and proteinuria. He had acute renal failure (urea 24.5 mmol/L, creatinine 341 µmol/L) and an elevated C-reactive protein (356 mg/L). Twelve-lead electrocardiograph demonstrated anterolateral T-wave inversion and troponin T was elevated (0.176 ng/mL), suggesting an acute coronary syndrome. Ultrasound of renal tracts was normal. Group B haemolytic
Mural endocarditis in the absence of pre-disposing factors is extremely rare. This condition is usually fatal; however, our patient was fortunate to survive and make a full recovery.
Panel A. Echocardiogram demonstrating apical vegetation. LV, left ventricle; RV, right ventricle.
Panel B. CT scan of brain demonstrating an infarct adjacent to the right caudate nucleus.
Panel C. Radioisotope-labelled white cell scan with focal uptake at the apex of the left ventricle.
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