Superior vena cava syndrome – changing etiology in the third millennium

Author:

Herscovici R1,Szyper-Kravitz M12,Altman A1,Eshet Y3,Nevo M1,Agmon-Levin N12,Shoenfeld Y124

Affiliation:

1. Department of Internal Medicine B, Sheba Medical Center, Tel Hashomer, Israel

2. The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel

3. Imaging Department, Sheba Medical Center, Israel

4. Incumbent of the Laura Schwartz-Kipp Chair for Autoimmunity, Tel Aviv University, Israel

Abstract

Superior vena cava syndrome (SVCS), is diagnosed following different degrees of central venous system obstruction, which traditionally was caused by infections, tumors or fibrosing mediastinitis. Recently the role of SVC thrombosis secondary to indwelling central venous devices or pacemaker leads as well as different hypercoagulable states have drawn much attention. In the current review we present a 58-year-old female patient who underwent recurrent pacemaker replacements due to recurrent infections. The patient was hospitalized with superior vena cava syndrome and multiple thrombi in the upper body circulation. Additionally the evaluation was conducted for thrombophilia, which revealed the presence of high titers of antiphospholipid antibodies, suggesting the concurrent diagnosis of the antiphospholipid syndrome (APS). This case reflects the changes in the etiology of SVCS, and the need for a comprehensive evaluation of patients, in the search for additional factors that may complicate a pacemaker insertion, such as the presence of antiphospholipid antibodies. We review the relevant literature and highlight the importance for an interdisciplinary approach in the treatment of SVCS nowadays.

Publisher

SAGE Publications

Subject

Rheumatology

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