Hereditary haemorrhagic telangiectasia: A case report.

Abstract

BACKGROUND:

Hereditary haemorrhagic telangiectasia is an autosomal dominant genetic disorder characterized by abnormalities in blood vessel formation. The clinical manifestations of patients affected with hereditary haemorrhagic telangiectasia include mucocutaneous telangiectasias and visceral arteriovenous malformations.

CASE SUMMARY:

We report the case of a 30-year-old female diagnosed with hereditary haemorrhagic telangiectasia presenting with the classic triad of recurrent epistaxis, mucocutaneous telangiectasias and family history of hereditary haemorrhagic telangiectasia with activin receptor-like kinase 1 mutation. Upon skin examination, she was noted to have telangiectasias under left naris, inner lower lip and surface of the tongue, and a vascular malformation on the right forearm.

CONCLUSION:

Although the skin involvement and epistaxis may be mild symptoms and signs of hereditary haemorrhagic telangiectasia, timely recognition of these can ensure vigilant monitoring of potential severe complications from cerebral and pulmonary visceral arteriovenous malformations.

• Authors: Asfandyar Mufti, Muskaan Sachdeva, Khalad Maliyar, Marissa Joseph
• Journal: SAGE open medical case reports (SAGE Open Med Case Rep) Vol. 9 Pg. 2050313X211003076 ( 2021) ISSN: 2050-313X [Print] England
• PMID: 34394937 (Publication Type: Case Reports)
• Copyright: © The Author(s) 2021.