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Maria Stella Graziani

Deputy Director
Martina Zaninotto

Associate Editors
Ferruccio Ceriotti
Davide Giavarina
Bruna Lo Sasso
Giampaolo Merlini
Martina Montagnana
Andrea Mosca
Paola Pezzati
Rossella Tomaiuolo
Matteo Vidali

EIC Assistant
Francesco Busardò

International Advisory Board Khosrow Adeli Canada
Sergio Bernardini Italy
Marcello Ciaccio Italy
Eleftherios Diamandis Canada
Philippe Gillery France
Kjell Grankvist Sweden
Hans Jacobs The Netherlands
Eric Kilpatrick UK
Magdalena Krintus Poland
Giuseppe Lippi Italy
Mario Plebani Italy
Sverre Sandberg Norway
Ana-Maria Simundic Croatia
Tommaso Trenti Italy
Cas Weykamp The Netherlands
Maria Willrich USA
Paul Yip Canada

Biomedia srl
Via L. Temolo 4, 20126 Milano

Responsible Editor
Giuseppe Agosta

Editorial Secretary
Chiara Riva
Biomedia srl
Via L. Temolo 4, 20126 Milano
Tel. 0245498282


ISSN print: 0393 – 0564
ISSN digital: 0392- 7091

BC: Articoli scritti da C. Giaccherini

Trombocitosi e rischio trombotico nelle neoplasie mieloproliferative
Thrombocytosis and risk of thrombosis in myeloproliferative neoplasms
<p>In patients with polycythemia vera (PV) and essential thrombocythemia (ET), two Philadelphia chromosome&ndash;negative myeloproliferative neoplasms (MPN), thrombotic events are frequent and represent the main cause of morbidity and mortality. Patients with MPN can be stratified in thrombotic risk categories according to age and history of thrombosis. Patients older than 60 years or with a history of thrombosis are considered at high-risk. Recently, new developments have brought to a further subcategorization of patients who are not at high risk in the &ldquo;intermediate&rdquo; and &ldquo;low-risk&rdquo; categories, depending on the presence or absence of <em>JAK2V617F</em> mutation and/or cardiovascular risk factors. Thrombocytosis is typical of these diseases, particularly of ET, but its role in the pathogenesis of thrombotic events is still controversial. So far, no study has demonstrated a statistically significant correlation between platelet count and thrombosis in either PV or ET patients. Paradoxically, extreme thrombocytosis (i.e., platelets &gt;1500&times;10<sup>9</sup>/L) is rather associated with hemorrhagic manifestations in patients with ET. Recent biological studies of circulating thrombotic markers performed to characterize the presence of a hypercoagulable state in patients with MPN have shown that platelet qualitative abnormalities, more than platelet count, are associated with hypercoagulability in these patients. Particularly, studies have demonstrated that platelets circulate in an activated status and possess a high prothrombotic potential. These findings suggest that in these diseases the control of platelet activation over the platelet count is an important goal of treatment strategies.</p>
Biochimica Clinica ; 41(2) 128-133
Rassegne - Reviews