The American Journal of Medicine
Volume 122, Issue 12 , Pages 1128-1135, December 2009

Cryofibrinogenemia: New Insights into Clinical and Pathogenic Features

  • David Saadoun, MD, PhD

      Affiliations

    • Pierre et Marie Curie-Paris 6 University, Department of Internal Medicine, Hôpital Pitié-Salpétrière, Paris, France
  • ,
  • Ismail Elalamy, MD, PhD

      Affiliations

    • Laboratory of Haemostasis, Hôpital Tenon, Paris, France
  • ,
  • Pascale Ghillani-Dalbin

      Affiliations

    • Laboratory of Immunochemistry, Hôpital Pitié-Salpétrière, Paris, France
  • ,
  • Damien Sene, MD, PhD

      Affiliations

    • Pierre et Marie Curie-Paris 6 University, Department of Internal Medicine, Hôpital Pitié-Salpétrière, Paris, France
  • ,
  • Aurelien Delluc, MD

      Affiliations

    • Pierre et Marie Curie-Paris 6 University, Department of Internal Medicine, Hôpital Pitié-Salpétrière, Paris, France
  • ,
  • Patrice Cacoub, MD, PhD

      Affiliations

    • Pierre et Marie Curie-Paris 6 University, Department of Internal Medicine, Hôpital Pitié-Salpétrière, Paris, France
    • Corresponding Author InformationReprint requests should be addressed to Patrice Cacoub, MD, PhD, Department of Internal Medicine, Université Pierre et Marie Curie-Paris 6, CNRS, UMR 7087, Paris, F-75013 France

Abstract 

Objective

Cryofibrinogenemia is an under-recognized cryoprotein that can be life-threatening when untreated. Our aim was to describe the prevalence and clinical findings of patients with cryofibrinogenemia and to clarify the mechanisms involved.

Methods

Between 1996 and 2006, 2312 patients were tested for cryofibrinogenemia in a single university hospital. A total of 515 patients had positive test results, of whom 455 (88.3%) had an associated cryoglobulin.

Results

Sixty patients (11.7%) with persistent cryofibrinogenemia and without cryoglobulin were included in the study. Main clinical manifestations related to cryofibrinogenemia included purpura (46.6%), skin necrosis (36.6%), and arthralgia (31.6%) with cold sensitivity in 40%. Overall thrombotic events occurred in up to 40% of cases. Cryofibrinogen plasma concentration was 2 times greater in patients with thrombotic events (P=.012). Complications included gangrene (5%), septicemia (5%), and leg amputation (3.3%). Complete remission of cryofibrinogenemia was achieved in 78% of patients receiving antithrombotic agents, steroids, or immunosuppressants, whereas 41.6% of patients experienced a relapse after a median time of 9 months (range 7-42 months). After a mean follow-up of 85 months, 3 patients died of sepsis (n=2) and cardiovascular disease (n=1). Fibrinolysis status analyzed in a patient with cryofibrinogenemia showed an increase in fibrinolysis inhibitor levels, plasminogen activator inhibitor-1, alpha-2 macroglobulin, and euglobulin lysis time, which normalized after fibrinolytic therapy.

Conclusion

Essential cryofibrinogenemia represents 12% of all the cryoproteins at Pitie-Salpêtriere Hospital. Thrombotic events are frequent and could be associated with the amount of plasma cryofibrinogen. Defects in the fibrinolysis process might lead to cryofibrinogen accumulation and clotting in small and medium arteries.

Keywords: Cryofibrinogenemia, Cryoproteins, Fibrinolysis, Vasculitis

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 Funding: Pierre et Marie Curie-Paris 6 University and AP-HP, Hôpital Pitié-Salpêtrière, Paris, France.

 Conflict of Interest: None of the authors have any conflicts of interest associated with the work presented in this manuscript.

 Authorship: All authors had access to the data and played a role in writing this manuscript.

PII: S0002-9343(09)00774-8

doi:10.1016/j.amjmed.2009.03.040

The American Journal of Medicine
Volume 122, Issue 12 , Pages 1128-1135, December 2009