Idiopathic hypereosinophilic syndrome with cutaneous involvement: a comparative review of 32 cases.

Research paper by Faisal F Inayat, Stacey S SS O'Neill, Fahad F Zafar, Sindhuja S Marupudi, Izzah I Vasim

Indexed on: 21 Dec '18Published on: 21 Dec '18Published in: BMJ case reports


Although idiopathic hypereosinophilic syndrome (HES) is uncommon, we studied the clinical characteristics of this disorder in patients with cutaneous involvement. We chronicle the case of a patient with diffuse skin rash due to idiopathic HES from our clinical experience. Furthermore, a systematic literature search of the medical databases PubMed and Google Scholar was conducted. A total of 32 cases fulfilled the inclusion criteria. The data on patients' characteristics, epidemiology, clinical features, diagnosis, treatment and outcome were collected and analysed. This review illustrates that physicians should maintain a high index of clinical suspicion for idiopathic HES in patients presenting with dermatological lesions and hypereosinophilia, without an obvious cause. Randomised clinical trials are warranted to outline a generalised and efficient therapeutic approach in these patients. Additionally, this paper highlights the need for population-based studies to delineate the magnitude and scope of this association. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.