| Literature DB >> 21480140 |
M Cikirikcioglu1, V C Keil, S M Cherian, T Theologou, P Merlani, H Muller, M-J Licker, A Kalangos.
Abstract
Primary cardiac lymphomas (PCL) are extremely rare, and diffuse large B-cell lymphoma is a highly aggressive subtype. We report a case that was initially diagnosed as chronic right heart dysfunction. Detailed investigations revealed a large lobulated tumour occluding the right atrium, infiltrating the inter-atrial septum, the roof of the left atrium, and the aortic root. Despite adequate surgical debulking and initial successful tricuspid annuloplasty, the patient succumbed to multi-organ failure. Pathological analysis of the resected tumour confirmed a diffuse large B-cell lymphoma with a proliferation rate of 100%. What is unique about this case is the size of this rare cardiac tumour, which we believe to be one of the largest described in the literature for a purely intra-cardiac PCL, its aggressive growth rate, and the relatively mild symptomatology until a late stage of the disease. © Georg Thieme Verlag KG Stuttgart · New York.Entities:
Mesh:
Year: 2011 PMID: 21480140 DOI: 10.1055/s-0030-1250342
Source DB: PubMed Journal: Thorac Cardiovasc Surg ISSN: 0171-6425 Impact factor: 1.827