Affiliation:
1. Cardiology department, CHRU Brabois, 1 rue du Morvan, Vandoeuvre les Nancy 54500, France
Abstract
Abstract
Background
Cardiac involvement in Sneddon syndrome (SS) is rare, the physiopathology is still unclear. We report a first case of SS without antiphospholipid antibodies who had coexisting ischaemia with no obstructive coronary arteries and aortic valve diseases.
Case summary
A 34-year-old woman with SS without antiphospholipid antibodies, was admitted for aphasia, and paresthaesia with confirmed right opercular ischaemic lesions at brain magnetic resonance imaging. Transthoracic echocardiographic examination showed akinesis of apical segments, moderate aortic valve stenosis, and moderate aortic insufficiency. Coronary angiogram was normal. Cardiac magnetic resonance showed transmural necrosis in the territory of the left anterior descending artery. Seven years later, our patient had no change or progression of myocardial ischaemic lesions or valvular disease.
Conclusion
We will discuss different hypothesis, diagnosis, treatment, and evolution of cardiac involvement in SS. Close follow-up should be regularly performed for early diagnosis, hence the importance of multimodality imaging, to guide treatment and prevent further complications.
Publisher
Oxford University Press (OUP)
Subject
Cardiology and Cardiovascular Medicine
Reference16 articles.
1. Sneddon’s syndrome: a long-term follow-up of 21 patients;Zelger;Arch Dermatol,1993
2. Cerebro-vascular lesions and livedo reticularis;Sneddon;Br J Dermatol,1965
3. Sneddon syndrome with or without antiphospholipid antibodies. A comparative study in 46 patients;Frances;Medicine,1999
4. Sneddon’s syndrome as a disorder of small arteries with endothelial cells proliferation: ultrastructural and neuroimaging study;Lewandowska;Folia Neuropathol,2005
5. Cutaneous manifestations of antiphospholipid antibody syndrome;Weinstein;Hematol Oncol Clin North Am,2008