Giant cell arteritis versus Takayasu's Arteritis: Two sides of the same coin?

Saudi J Ophthalmol

Department of Ophthalmology, Blanton Eye Institute, Houston Methodist Hospital, Houston, TX, USA.

Published: April 2022

AI Article Synopsis

  • There are different types of vasculitides, classified by factors like the size and location of affected vessels, histopathological differences, genetics, and the age of onset.* -
  • Takayasu's arteritis (TkA) and giant cell arteritis (GCA) are the primary medium to large vessel vasculitides, each with unique characteristics and treatments but sharing some similarities in their features.* -
  • The article explores the genetics, histopathology, and mechanisms behind both TkA and GCA, raising questions about whether they are distinct diseases or variations of the same underlying process.*

Article Abstract

There are multiple vasculitides which are distinguished based on multiple criteria, including size of affected vessels, distribution of vessels affected, histopathologic differences, genetic factors, and age at presentation. Takayasu's arteritis (TkA) and giant cell arteritis (GCA) are the two main medium to large vessel vasculitides. These vasculitides are associated with different racial predilections, vascular distributions, age groups, diagnostic criteria, and treatments. Nevertheless, the many shared histopathologic features, genetic factors, and overlap in presentation of these two diseases suggest that they may actually be variable presentations of the same disease process, i.e., large vessel vasculitis. This article will review the genetics, histopathology, disease mechanisms, and diagnostic criteria for both TkA and GCA. Overall, despite major advances our understanding of these two diseases, it is still debated whether these two large vessel vasculitides represent two distinct diseases processes or simply variations of the same disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116096PMC
http://dx.doi.org/10.4103/SJOPT.SJOPT_152_21DOI Listing

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