Persistent hypereosinophilia with Wells syndrome

Authors

Errata

This article is corrected by:

  1. Errata: Corrigendum Volume 38, Issue 3, 330, Article first published online: 21 March 2013

  • Conflict of interest: none declared.

Dr James Powell, Department of Dermatology, Worcestershire Royal Hospital, Worcester WR5 1DD, UK
E-mail: jbpowell@doctors.org.uk

Summary

Since Wells and Smith first described cases of eosinophilic cellulitis (Wells syndrome; WS) in 1979, it has been noted that some but not all patients with WS present with eosinophilia. In the face of idiopathic persistent eosinophilia patients will also then fall within the hypereosinophilic syndrome (HES), which represents a multifarious spectrum of disorders of varying severity, causes and outcomes. In this article we propose that patients who present within the HES spectrum with cutaneous findings of WS and with no extracutaneous disease be classified as having ‘persistent hypereosinophilia with Wells syndrome’ (PHEWS).

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