Acta Medica Martiniana (Dec 2018)

Severe Recurrent Epistaxis - The Main Symptom of Hereditary Haemorrhagic Teleangiectasia

  • Lucanska M,
  • Hajtman A,
  • Pecova R

DOI
https://doi.org/10.2478/acm-2018-0016
Journal volume & issue
Vol. 18, no. 3
pp. 42 – 48

Abstract

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Hereditary haemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is of dominant autosomal inheritance. Pathologic changes of vascular walls cause recurrent episodes of bleeding from many organ systems. Recurrent epistaxis is the first and the most frequent symptom of HHT. The causal therapy is not known but there are many therapeutic procedures improving the overall condition.

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