The Pan African Medical Journal (Nov 2016)

Hereditary hemorrhagic telangiectasia patient presenting with brain abscess due to silent pulmonary arteriovenous malformation

  • Marios Themistocleous,
  • Dimitrios Giakoumettis,
  • Andreas Mitsios,
  • Christos Anagnostopoulos,
  • Aristoteles Kalyvas,
  • Christos Koutsarnakis

DOI
https://doi.org/10.11604/pamj.2016.25.145.11010
Journal volume & issue
Vol. 25, no. 145

Abstract

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Hereditary hemorrhagic telangiectasia is a rare autosomal dominant inherited disease that is usually complicated by visceral vascular malformations. Patients harboring such malformations are at increased risk of brain abscess formation, which despite advances in diagnostic and surgical methods remains a life threatening medical emergency with high mortality and morbidity rates. In the present report we describe a case of cerebral abscess due to silent pulmonary arteriovenous malformation (AVM) in a young patient previously undiagnosed for hereditary hemorrhagic telangiectasia syndrome (HHT).

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