Brain abscess and hereditary hemorrhagic telangiectasia.
Publication/Presentation Date
6-1-2008
Abstract
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disorder that can lead to serious central nervous system complications including hemorrhage, ischemia, and infection. Symptoms can be mild, making diagnosis problematic. Fifty-three prior cases of HHT and brain abscess are described, in addition to two new cases. The clinical manifestations and current methods for diagnosis and management of patients with HHT are reviewed. Early recognition of HHT is important because screening in these patients and affected family members may help prevent complications. In addition, advancements in imaging, surgical techniques, antibiotics, and genetic testing may improve outcomes.
Volume
101
Issue
6
First Page
618
Last Page
625
ISSN
1541-8243
Published In/Presented At
Sell, B., Evans, J., & Horn, D. (2008). Brain abscess and hereditary hemorrhagic telangiectasia. Southern medical journal, 101(6), 618–625. https://doi.org/10.1097/SMJ.0b013e318172f716
Disciplines
Business Administration, Management, and Operations | Health and Medical Administration | Management Sciences and Quantitative Methods
PubMedID
18475224
Department(s)
Administration and Leadership
Document Type
Article