4.7 Review

How I treat hypereosinophilic syndromes

Journal

BLOOD
Volume 114, Issue 18, Pages 3736-3741

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2009-07-143552

Keywords

-

Categories

Funding

  1. National Institutes of Health (NIH), National Institute of Allergy and Infectious Diseases (NIAID)

Ask authors/readers for more resources

Hypereosinophilic syndromes (HESs) are a heterogeneous group of uncommon disorders characterized by marked peripheral eosinophilia and end organ manifestations attributable to the eosinophilia or unexplained in the clinical setting. Whereas corticosteroids remain the main-stay of treatment for most patients, recent diagnostic advances and the development of novel targeted therapies, including tyrosine kinase inhibitors and humanized monoclonal antibodies, have increased the complexity of therapeutic decisions in HESs. This review presents a treatment-based approach to the diagnosis and classification of patients with peripheral blood eosinophilia of 1.5 x 10(9)/L (1500/mm(3)) or higher and discusses the role of currently available therapeutic agents in the treatment of these patients. (Blood. 2009; 114: 3736-3741)

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available