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Research Article| Volume 160, ISSUE 2, P207-211, August 1990

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A contemporary perspective on superior vena cava syndrome

  • Author Footnotes
    1 From the Department of Surgery, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance, California.
    John C. Chen
    Footnotes
    1 From the Department of Surgery, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance, California.
    Affiliations
    Torrance, California, USA
    Search for articles by this author
  • Author Footnotes
    1 From the Department of Surgery, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance, California.
    Fred Bongard
    Footnotes
    1 From the Department of Surgery, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance, California.
    Affiliations
    Torrance, California, USA
    Search for articles by this author
  • Author Footnotes
    1 From the Department of Surgery, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance, California.
    Stanley R. Klein
    Correspondence
    Requests for reprints should be addressed to Stanley R. Klein, MD, Department of Surgery, Harbor-UCLA Medical Center, UCLA School of Medicine, 1000 West Carson Street, Box 15, Torrance, California 90509.
    Footnotes
    1 From the Department of Surgery, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance, California.
    Affiliations
    Torrance, California, USA
    Search for articles by this author
  • Author Footnotes
    1 From the Department of Surgery, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance, California.
      This paper is only available as a PDF. To read, Please Download here.
      The superior vena cava (SVC) syndrome is usually associated with advanced malignancy and has a dismal prognosis. In order to analyze the impact of newer diagnostic and therapeutic modalities, we retrospectively examined the last 45 consecutive cases of SVC syndrome treated over a 12-year period. The underlying causes were advanced lung cancer (57%), mediastinal tumors (20%), and metastatic solid malignancy (5%). Forty-two patients (93%) were treated with external beam radiotherapy and/or chemotherapy with a mean patient survival of 3 months; 11 of 42 patients (26%) were treated without histologic diagnosis. Symptoms of SVC obstruction resolved in 80% of patients who underwent radiotherapy, with a mean interval of 4 weeks. The most common cause of death was respiratory arrest. Of the three patients with benign disease, two underwent caval reconstruction with greater than 3-year patency and relief of symptoms.
      We conclude that (1) SVC syndrome portends a grim prognosis when associated with malignancy but usually responds to radiation or chemotherapy; (2) CT scan is the best available method to document the extent and location of involvement; and (3) patients with benign disease should be evaluated for caval reconstruction, which may produce rewarding long-term results.
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