Presentation and Classification of Rare Primary Vasculitides in ChildrenLythgoe Hanna1,2*, Guratsky V3 and Baildam E3
- Corresponding Author:
- Lythgoe Hanna
Department of Women’s and Children’s Health
Institute of Translational Medicine, University of Liverpool, UK
Tel: 0151 228 4811
Fax: 0151 228 0328
E-mail: [email protected]
Received date: April 21, 2016; Accepted date: May 05, 2016; Published date: May 08, 2016
Citation: Hanna L, Guratsky V, Baildam E (2016) Presentation and Classification of Rare Primary Vasculitides in Children. J Vasc 2:107. doi: 10.4172/2471-9544.1000107
Copyright: © 2016 Hanna L, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Primary vasculitides, where blood vessels are the primary site of inflammation, with the exception of Henoch Schönlein purpura (HSP) and Kawasaki’s disease (KD) are rare in childhood but when present, cause significant morbidity and mortality. This review provides an update on classification and presentation of rare vasculitides in children, through considering our experience in three cases in context with the current literature. We have demonstrated the challenges to diagnosis and how diagnosis can easily be missed if vasculitides are not carefully considered and looked for. The introduction of classification criteria has been important to allow more research into rare paediatric vasculitides but development of diagnostic criteria may be useful. Vasculitides should be considered in all patients presenting with multi-system features.