Literature DB >> 25596963

Acquired factor XI deficiency: a rare complication after liver transplantation.

Y Yankol1, N Mecit2, T Kanmaz2, K Acarli2, M Kalayoglu2.   

Abstract

BACKGROUND: A majority of coagulation factors are synthesized in the liver. Factor XI (FXI) deficiency (Rosenthal syndrome) is one of the rare inherited coagulation disorders with an extremely low risk of transmission by liver transplantation (LT). CASE REPORT: We report here the case of a 50-year-old man who unknowingly acquired FXI deficiency by LT. During 1 year of post-transplant follow-up, his activated partial thromboplastin time (aPTT) remained prolonged, but he did not develop bleeding complications. The patient required retransplantation due to chronic rejection and is currently doing well 4 years after his first liver transplantation.
CONCLUSIONS: The presence of a prolonged aPTT in a deceased donor should raise suspicion for the presence of rare coagulation factor deficiencies. During urgent, lifesaving procedures such as LT, it may be impossible to avoid transmission. Awareness of this possibility will allow early detection and management.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 25596963     DOI: 10.1016/j.transproceed.2014.10.042

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  2 in total

1.  Donor-to-recipient transmission of factor XII deficiency by orthotopic liver transplantation.

Authors:  Hussien Elsiesy; Mohamed Shawakat; Waleed Alhamoudi; Mohamed Alsebayel; John Renz; Hany Elbeshbeshy; Mohamed Abdelfattah; Faisal Abaalkhail
Journal:  Proc (Bayl Univ Med Cent)       Date:  2019-08-19

2.  Case of concurrent factor VII and factor XI deficiencies manifesting as spontaneous lower extremity compartment syndrome.

Authors:  Joseph P Marshalek; David Yashar; Karen Huynh; Sarah Tomassetti
Journal:  Clin Case Rep       Date:  2022-04-25
  2 in total

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