A case series on recurrent and persisting IgA vasculitis (Henoch Schonlein purpura) in children.

ABSTRACT:

Background

IgA vasculitis (IgAV) is a small vessel vasculitis that is more common in childhood. Very limited evidence exists on patients who experience an atypical disease course. The aim of this study was to describe a cohort of children diagnosed with recurrent or persisting IgAV to identify any themes associated with their disease course and areas of unmet needs.

Methods

A single centre retrospective study of children diagnosed with recurrent or persisting IgAV at Alder Hey Children's Hospital (Liverpool, UK). Clinical data, including features at presentation and during follow up, potential triggers, abnormal laboratory and histology results, treatment and outcome at last clinical review were retrospectively collected. Key themes were identified.

Results

A total of

SUBMITTER: Marro J 

PROVIDER: S-EPMC10424434 | biostudies-literature | 2023 Aug

REPOSITORIES: biostudies-literature