Phlebologie 2017; 46(01): 31-33
DOI: 10.12687/phleb2345-1-2017
Case report
Schattauer GmbH

Recurrent vein thrombosis with agenesis of the inferior vena cava and AT III deficiency

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Authors

  • J. Lukaseder

    Krankenhaus Hietzing mit Neurologischem Zentrum Rosenhügel, Abteilung für Dermatologie, Wien, Austria
  • R. Feldmann

    Krankenhaus Hietzing mit Neurologischem Zentrum Rosenhügel, Abteilung für Dermatologie, Wien, Austria
  • A. Steiner

    Krankenhaus Hietzing mit Neurologischem Zentrum Rosenhügel, Abteilung für Dermatologie, Wien, Austria
Weitere Informationen

Publikationsverlauf

Received: 24. November 2016

Accepted: 23. Dezember 2016

Publikationsdatum:
05. Januar 2018 (online)

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Summary

Abnormalities of vena cava inferior are rare malformations and are often discovered by chance . While patients with duplication or left-sided position of the vena cava inferior rarley become clinically apparent the agenesis of the vena cava is associated with an increased rate of deep vein thrombosis. We report a 36-year-old man with recurrent venous thrombosis in which a computer thomography the suspected diagnosis of vena cava inferior agenesis secures and thus a lifelong anticoagulation indicates.