Investigation of acquired von Willebrand Syndrome in children with hypothyroidism: reversal after treatment with thyroxine

J Pediatr Endocrinol Metab. 2010 Sep;23(9):967-74.

Abstract

Background: Acquired von Willebrand Syndrome (AvWS) is a rare bleeding disorder associated with various underlying conditions. Many case reports have been published so far on bleeding tendency in hypothyroidism resembling AvWS.

Objective: This study was designed to define the relationship between hypothyroidism and AvWS and to investigate the effects of L-thyroxine treatment.

Subjects: Twenty four hypothyroid patients were included in the study. Nineteen patients were evaluated during treatment, 5 patients were evaluated before hormone replacement.

Methods: Complete coagulation screening tests including levels of von Willebrand Factor antigen (vWF:Ag) and functional activity (vWF:RCo) were measured by thrombocyte aggregometer.

Results: We demonstrated low vWF:Ag and vWF:RCo in 13 patients. Two of the 13 patients were diagnosed as AvWS, while another 2 patients were diagnosed as hereditary vWD Type 1. The remaining patients are still being followed-up.

Conclusion: We would like to attract the attention of paediatricians to the possibility of bleeding due to decreased activity of vWF in hypothyroid children.

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Hypothyroidism / blood*
  • Hypothyroidism / complications
  • Hypothyroidism / drug therapy
  • Infant
  • Infant, Newborn
  • Male
  • Thyroxine / therapeutic use*
  • von Willebrand Diseases / etiology*

Substances

  • Thyroxine