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Neurologic Manifestation as Initial Presentation in a Case of Hereditary Haemorrhagic Telangiectasia
Author(s) -
Yeow Kwan Teo,
Ai Ching Kor
Publication year - 2010
Publication title -
clinical medicine insights case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.187
H-Index - 12
ISSN - 1179-5476
DOI - 10.4137/ccrep.s4749
Subject(s) - telangiectasia , medicine , presentation (obstetrics) , brain abscess , telangiectases , pathology , abscess , surgery
Hereditary Haemorrhagic Telangiectasia (HHT), or Osler-Weber-Rendu syndrome is an uncommon autosomal dominant multi-organ condition of vascular dysplasias. We describe a 19 year old Indian female who presented with cerebral abscess secondary to paradoxical emboli from pulmonary arteriovenous malformations (PAVMs) associated with HHT. Cerebral, pulmonary, hepatic and gastrointestinal involvement can be life-threatening and it is important to have lifelong follow-ups on these patients.

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