Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2015) 37 EP1321 | DOI: 10.1530/endoabs.37.EP1321

ECE2015 Eposter Presentations Clinical Cases–Thyroid/Other (101 abstracts)

Can pericardial effusion be a manifestation of Graves' disease? An unusual case

George Besis 1 , Nikolaos Kyriakakis 2 & Lakdasa D Premawardhana 3


1Department of Cardiology, University Hospital of Wales, Cardiff, UK; 2Leeds Centre for Diabetes and Endocrinology, St James’s University Hospital, Leeds Teaching Hospitals NHS Trust, Leeds, UK; 3Section of Endocrinology, Department of Medicine, Ysbyty Ystrad Fawr, Hengoed, UK.


Introduction: Graves’ disease (GD) is associated with a number of cardiovascular complications, including rhythm disturbances, mitral valve prolapse, pulmonary hypertension and heart failure. Pericardial effusion in the context of GD has only been reported in a small number of cases.

Case: A 59-year-old gentleman presented with a 3-day history of dyspnoea and pleuritic chest pain. He had a previous history of GD 8 months ago, pulmonary embolism (PE), asthma, hypertension, obesity and was established on warfarin, following a second episode of PE, 4 weeks prior to this clinical event. Clinical examination revealed tachypnoea, tachycardia, raised JVP and bibasal crackles. Echocardiography showed a 2.9 cm pericardial effusion, compromising the right ventricular filling. 10 days prior to this admission, a previously echocardiogram had shown a smaller size pericardial effusion. TFTs showed suppressed TSH, elevated free T4 at 34.7 pmol/l (reference range 9.2–21 pmol/l) and positive TSH receptor antibodies, compatible with relapsed GD. Other laboratory investigations showed acute kidney injury (eGFR 38 ml/min per 1.73 m2) and elevated INR at 17.2, which was pharmacologically reversed. Interestingly, 10 days prior to admission the patient had normal renal function. Analysis of the pericardial fluid showed inflammatory cells. Microbiology and cytology investigations were unremarkable. A full body CT scan did not show evidence of neoplastic process. The patient was stabilised following pericardiocentesis and was commenced on Carbimazole 40 mg daily.

Conclusions: This is an unusual presentation of GD. The patient was investigated extensively, but no alternative cause for pericardial effusion was found. The presence of inflammatory cells in the fluid, suggests an inflammatory pericarditis. GD could have also been implicated in the pathogenesis of the patient’s recent PE, given the thrombogenic tendency that hyperthyroidism is associated with. We therefore recommend that TFTs should be undertaken in patients presenting with unexplained pericardial effusion and equally patients with GD presenting with dyspnoea should undergo echocardiography.

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