<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kluin-Nelemans HC</submitter><funding>Austrian Science Fund FWF</funding><funding>Deutsche Forschungsgemeinschaft</funding><pagination>1090-1101</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7115841</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>34(4)</volume><pubmed_abstract>Systemic mastocytosis (SM) is frequently associated with eosinophilia. To examine its prevalence and clinical impact in all WHO classification-based subcategories, we analyzed eosinophil counts in 2350 mastocytosis patients using the dataset of the European Competence Network on Mastocytosis. Ninety percent of patients had normal eosinophil counts, 6.8% mild eosinophilia (0.5-1.5 × 10&lt;sup>9&lt;/sup>/l), and 3.1% hypereosinophilia (HE; >1.5 × 10&lt;sup>9&lt;/sup>/l). Eosinophilia/HE were mainly present in patients with advanced SM (17%/19%), and only rarely recorded in patients with indolent and smoldering SM (5%/1%), and some patients with cutaneous mastocytosis. The eosinophil count correlated with organomegaly, dysmyelopoiesis, and the WHO classification, but not with mediator-related symptoms or</pubmed_abstract><journal>Leukemia</journal><pubmed_title>Prognostic impact of eosinophils in mastocytosis: analysis of 2350 patients collected in the ECNM Registry.</pubmed_title><pmcid>PMC7115841</pmcid><funding_grant_id>F 4701</funding_grant_id><funding_grant_id>RA2838</funding_grant_id><funding_grant_id>F 4704</funding_grant_id><pubmed_authors>Shoumariyeh K</pubmed_authors><pubmed_authors>Zanotti R</pubmed_authors><pubmed_authors>Breynaert C</pubmed_authors><pubmed_authors>Panse J</pubmed_authors><pubmed_authors>Niedoszytko M</pubmed_authors><pubmed_authors>Mattsson M</pubmed_authors><pubmed_authors>Elena C</pubmed_authors><pubmed_authors>Rossignol J</pubmed_authors><pubmed_authors>Jawhar M</pubmed_authors><pubmed_authors>Scaffidi L</pubmed_authors><pubmed_authors>Niederwieser D</pubmed_authors><pubmed_authors>Fortina AB</pubmed_authors><pubmed_authors>Jakob T</pubmed_authors><pubmed_authors>Perkins C</pubmed_authors><pubmed_authors>Doubek M</pubmed_authors><pubmed_authors>Lortholary O</pubmed_authors><pubmed_authors>Parente R</pubmed_authors><pubmed_authors>Valent P</pubmed_authors><pubmed_authors>Gorska A</pubmed_authors><pubmed_authors>Varkonyi J</pubmed_authors><pubmed_authors>Sabato V</pubmed_authors><pubmed_authors>Illerhaus A</pubmed_authors><pubmed_authors>Lange M</pubmed_authors><pubmed_authors>Kilbertus A</pubmed_authors><pubmed_authors>Arock M</pubmed_authors><pubmed_authors>Aberer E</pubmed_authors><pubmed_authors>Gotlib J</pubmed_authors><pubmed_authors>Hagglund H</pubmed_authors><pubmed_authors>Hermine O</pubmed_authors><pubmed_authors>Zink A</pubmed_authors><pubmed_authors>Hartmann K</pubmed_authors><pubmed_authors>von Bubnoff N</pubmed_authors><pubmed_authors>Bonadonna P</pubmed_authors><pubmed_authors>Triggiani M</pubmed_authors><pubmed_authors>Schwaab J</pubmed_authors><pubmed_authors>van Anrooij B</pubmed_authors><pubmed_authors>Caroppo F</pubmed_authors><pubmed_authors>Kennedy V</pubmed_authors><pubmed_authors>Yavuz AS</pubmed_authors><pubmed_authors>Reiter A</pubmed_authors><pubmed_authors>Brockow K</pubmed_authors><pubmed_authors>Fuchs D</pubmed_authors><pubmed_authors>Sperr WR</pubmed_authors><pubmed_authors>Span LFR</pubmed_authors><pubmed_authors>Malcovati L</pubmed_authors><pubmed_authors>Kluin-Nelemans HC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prognostic impact of eosinophils in mastocytosis: analysis of 2350 patients collected in the ECNM Registry.</name><description>Systemic mastocytosis (SM) is frequently associated with eosinophilia. To examine its prevalence and clinical impact in all WHO classification-based subcategories, we analyzed eosinophil counts in 2350 mastocytosis patients using the dataset of the European Competence Network on Mastocytosis. Ninety percent of patients had normal eosinophil counts, 6.8% mild eosinophilia (0.5-1.5 × 10&lt;sup>9&lt;/sup>/l), and 3.1% hypereosinophilia (HE; >1.5 × 10&lt;sup>9&lt;/sup>/l). Eosinophilia/HE were mainly present in patients with advanced SM (17%/19%), and only rarely recorded in patients with indolent and smoldering SM (5%/1%), and some patients with cutaneous mastocytosis. The eosinophil count correlated with organomegaly, dysmyelopoiesis, and the WHO classification, but not with mediator-related symptoms or</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2025-04-21T20:14:23.521Z</modification><creation>2020-09-17T07:08:11Z</creation></dates><accession>S-EPMC7115841</accession><cross_references><pubmed>31740811</pubmed><doi>10.1038/s41375-019-0632-4</doi></cross_references></HashMap>