<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(1)</volume><submitter>Loscocco GG</submitter><pubmed_abstract>We describe 1000 patients with essential thrombocythemia seen at the Center Research and Innovation of Myeloproliferative Neoplasms (CRIMM), Florence, Italy, between 1980 and 2023: median age 59 years (18-95), females 65%, JAK2/CALR/MPL-mutated 66%/19%/4%, triple-negative (TN) 11%. Extreme thrombocytosis (ExT, platelets ≥1000 × 10&lt;sup>9&lt;/sup>/L) in 16%, leukocytosis (leukocytes >11 × 10&lt;sup>9&lt;/sup>/L) in 16%, and at least one cardiovascular risk factor in 52% of cases. JAK2-mutated patients were older (median 62 years) and CALR-mutated and TN (53 years for both) younger (p &lt; 0.001). Female gender clustered with TN (76%) and JAK2 (67%) vs CALR (46%) mutations (p &lt; 0.001). ExT clustered with CALR (type-2 more than type-1), TN and MPL, and leukocytosis with JAK2 mutation (p &lt; 0.001). In multi</pubmed_abstract><journal>Blood cancer journal</journal><pagination>10</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10796728</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>One thousand patients with essential thrombocythemia: the Florence-CRIMM experience.</pubmed_title><pmcid>PMC10796728</pmcid><pubmed_authors>Loscocco GG</pubmed_authors><pubmed_authors>Vannucchi AM</pubmed_authors><pubmed_authors>Capecchi G</pubmed_authors><pubmed_authors>Guglielmelli P</pubmed_authors><pubmed_authors>Atanasio A</pubmed_authors><pubmed_authors>Maccari C</pubmed_authors><pubmed_authors>Gesullo F</pubmed_authors><pubmed_authors>Mannelli F</pubmed_authors></additional><is_claimable>false</is_claimable><name>One thousand patients with essential thrombocythemia: the Florence-CRIMM experience.</name><description>We describe 1000 patients with essential thrombocythemia seen at the Center Research and Innovation of Myeloproliferative Neoplasms (CRIMM), Florence, Italy, between 1980 and 2023: median age 59 years (18-95), females 65%, JAK2/CALR/MPL-mutated 66%/19%/4%, triple-negative (TN) 11%. Extreme thrombocytosis (ExT, platelets ≥1000 × 10&lt;sup>9&lt;/sup>/L) in 16%, leukocytosis (leukocytes >11 × 10&lt;sup>9&lt;/sup>/L) in 16%, and at least one cardiovascular risk factor in 52% of cases. JAK2-mutated patients were older (median 62 years) and CALR-mutated and TN (53 years for both) younger (p &lt; 0.001). Female gender clustered with TN (76%) and JAK2 (67%) vs CALR (46%) mutations (p &lt; 0.001). ExT clustered with CALR (type-2 more than type-1), TN and MPL, and leukocytosis with JAK2 mutation (p &lt; 0.001). In multi</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2025-04-04T10:34:33.777Z</modification><creation>2025-04-04T10:34:33.777Z</creation></dates><accession>S-EPMC10796728</accession><cross_references><pubmed>38238287</pubmed><doi>10.1038/s41408-023-00968-7</doi></cross_references></HashMap>