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Myeloproliferative Disorders - Symptoms, Risk Factors and Treatment Options (Paperback)
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Myeloproliferative Disorders - Symptoms, Risk Factors and Treatment Options (Paperback)
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Myeloproliferative disorders are a group of clonal haematological
neoplasms characterised by proliferation of one or more cells of
myeloid lineage. They are the result of acquired mutations in the
progenitor cell leading to hyper proliferation or neoplastic
expansion of more mature forms of myeloid cells. Cells retain their
functional ability with some degree of defects and also lead to
suppression of normal stem cells. The most common type of
Myeloproliferative Neoplasms (MPN) can broadly be classified into
BCR ABL positive (Chronic Myelogenous Leukemia) and BCR ABL
negative Disorders (Polycythemia Vera PV, Essential Thrombocytosis
ET and Primary Myelofibrosis PMF). There are other rare types which
have relatively low incidence like chronic neutrophilic leukemia,
chronic eosinophilic leukemia, systemic mastocytosis and
myeloproliferative neoplasms unclassifiable. These are the indolent
type of haematological malignancies associated with marrow
hypercellularity and organomegaly, with gradual progression to
myelofibrosis or transformation to acute leukemias. During the
dormant course of the BCR ABL negative MPN, they are more prone to
thrombo-hemorrhagic complications and the treatment strategy is
directed mostly to prevent complications. The past decade;
therapies for BCR ABL positive disease (CML) have been a milestone
achievement in keeping the disease in remission for many years,
preventing major complications and halting the progression of the
disease. This book discusses the classification, diagnosis and
treatment of myeloproliferative diseases and provides insight on
the symptoms and risk factors involved in the diseases.
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