AI Article Synopsis

  • Primary myelofibrosis (PMF) and polycythaemia vera (PV) are uncommon blood disorders that can lead to serious complications like blood clots, bleeding, and potentially cancer.
  • These conditions exhibit diverse biological and clinical characteristics, making their management in everyday medical practice quite variable.
  • The review offers a recent perspective on diagnosing, predicting outcomes, and treating PMF and PV, highlighting how a group of experts in France applies research findings to standard healthcare practices.

Article Abstract

Primary myelofibrosis (PMF) and polycythaemia vera (PV) are rare -negative myeloproliferative neoplasms, associated with an increased risk of thrombosis, haemorrhagic complications and progression to fibrosis or leukaemia or fibrosis for PV. Both diseases are characterised by biological and clinical heterogeneity, leading to great variability in their management in routine clinical practice. In this review, we present an updated overview of the diagnosis, prognosis and treatment of PMF and PV, and we discuss how our multidisciplinary expert group based across France translates this evidence-based knowledge into routine clinical practice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435696PMC
http://dx.doi.org/10.1002/jha2.734DOI Listing

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