| Literature DB >> 28932580 |
Yoon Pyo Lee1, Eun Mi Chun1, Yoo Kyung Kim2, Kwan Chang Kim3.
Abstract
This report describes a rare case of benign superior vena cava syndrome (SVCS) accompanying recalcitrant pleural effusion developed secondary to extrinsic compression by anthracotic calcified mediastinal lymphadenopathy which was corrected by surgical bypass graft. An 81-year-old female presented with recalcitrant pleural effusion for several months despite of medical treatments. SVCS developed progressively without any other radiological evidence of malignancy or active infection on initial chest computed tomography (CT). A follow-up chest CT scan taken one month later revealed a poorly-defined mass-like lesion encasing the SVC. Near total collapse of the SVC due to circumferential compression by massive anthracotic calcified lymph nodes was noted in the surgical fields. A bypass graft was performed using an artificial vessel instead of endovascular treatment because of severe adhesion. The abrupt SVCS and uncontrolled pleural effusions completely disappeared after surgical correction.Entities:
Keywords: Superior vena cava syndrome (SVCS); mediastinal lymphadenopathy; pleural effusion
Year: 2017 PMID: 28932580 PMCID: PMC5594184 DOI: 10.21037/jtd.2017.06.51
Source DB: PubMed Journal: J Thorac Dis ISSN: 2072-1439 Impact factor: 2.895