Semin Thromb Hemost 1997; 23(3): 253-258
DOI: 10.1055/s-2007-996098
Copyright © 1997 by Thieme Medical Publishers, Inc.

APC Resistance in Childhood Thromboembolism: Diagnosis and Clinical Aspects

Ulrike Nowak-Göttl* , Reinhard Schneppenheim , Heinrich Vielhaber*
  • From the Departments of Pediatrics, University Hospitals *Münster
  • †Kiel, Germany.
Further Information

Publication History

Publication Date:
08 February 2008 (online)

Abstract

Few studies of activated protein C resistance (APCR) and thromboembolism in childhood have been published. In the majority of childhood thromboses reported, the factor V Leiden mutation was associated with venous thromboses; however, one case report and three studies described arterial thromboembolism in infants and children due to the common mutation in the factor V gene. In one neonate purpura fulminans occurred, and heparininduced thrombocytopenia type II was additionally documented. Two case reports and seven of nine studies reported associated clinical conditions together with inherited coagulation disorders. In three studies homozygous patients were mentioned.

There are few studies describing the interaction between APCR and coagulation or the fibrinolytic system in symptomatic and nonsymptomatic infants. Compared with healthy brothers or sisters and a healthy age-matched control group, thrombin generation, D-dimer, PAI-1 activity, and t-PA antigen were found clearly elevated in children with APCR. In addition, infants and children with the Arg506-to-Gln mutation in the factor V gene showed significantly increased thrombomodulin concentrations along with normal protein C activities compared with relatives and healthy controls. No difference was recorded in these studies between heterozygous infants and children without vascular occlusion and patients who previously had suffered from thromboembolism.

Until long-term data are available for the treatment of patients with APCR, such children should be treated in the same way as patients with deficiencies of protein C, protein S, or antithrombin.