| Literature DB >> 34053318 |
Janaki Devara1, Vivek N Iyer2, Deepti M Warad3, Waleed Brinjikji4, Ahmad Aljobeh5, Giuseppe Lanzino6, Nadir Demirel1.
Abstract
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant hereditary disorder that results in arteriovenous malformations (AVMs) in the nose, mucocutaneous surfaces and visceral organs, including lung, brain, liver, bowel and rarely spinal cord. We describe a case of a young child with HHT who presented with acute paraparesis due to acute thrombosis of a spinal perimedullary arteriovenous fistula. Patient underwent coil embolization of spinal arteriovenous shunt with resolution of clinical symptoms. This case highlights the possibility of catastrophic complications in young children with HHT, the potential preventive role of screening for spinal AVMs in HHT and the importance of timely intervention.Entities:
Keywords: Hereditary hemorrhagic telangiectasia; paresis; spinal arteriovenous malformations
Mesh:
Year: 2021 PMID: 34053318 PMCID: PMC9131508 DOI: 10.1177/15910199211022499
Source DB: PubMed Journal: Interv Neuroradiol ISSN: 1591-0199 Impact factor: 1.764