Thromb Haemost 1962; 07(03): 558-566
DOI: 10.1055/s-0038-1655405
Originalarbeiten — Original Articles — Travaux Originaux
Schattauer GmbH

Acquired Factor X Deficiency in a Patient with Amyloidosis

Autoren

  • Kristoffer Korsan-Bengtsen

    1   Medical Department II, Sahlgrenska Hospital, University of Göteborg, Sweden, and Institute for Thrombosis Research, University Hospital, Rikshospitalet, Oslo, Norway
  • Peter F Hjort

    1   Medical Department II, Sahlgrenska Hospital, University of Göteborg, Sweden, and Institute for Thrombosis Research, University Hospital, Rikshospitalet, Oslo, Norway
  • Johan Ygge

    1   Medical Department II, Sahlgrenska Hospital, University of Göteborg, Sweden, and Institute for Thrombosis Research, University Hospital, Rikshospitalet, Oslo, Norway
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
21. Juni 2018 (online)

Summary

A patient with extensive amyloidosis and a selective factor X deficiency is described. The following observations indicate that the factor X deficiency in this case is not inherited.

1. The first symptoms of a bleeding tendency appeared at an age of 50 years.

2. The patient’s four children had no clotting defect.

3. After infusion of 1 liter of fresh plasma no increased factor X activity was observed. No anticoagulants could be demonstrated in vitro.