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- W2065514210 endingPage "767" @default.
- W2065514210 startingPage "751" @default.
- W2065514210 abstract "Idiopathic myelofibrosis is the least common and carries the worst prognosis of the chronic myeloproliferative disorders. The primary disease process is a clonal haematopoietic stem cell disorder which results in a chronic myeloproliferation and an atypical megakaryocyte hyperplasia. In contrast, the characteristic stromal proliferation is a reactive phenomenon, resulting from the inappropriate release of megakaryocyte/platelet-derived growth factors, including PDGF, TGF-beta bFGF and calmodulin. The median survival is approximately 4 years, although individual survival varies greatly. A variety of prognostic schema have been developed which enable the identification of high-risk patients, for whom bone marrow transplantation should be considered. Management for the majority of patients, however, is directed towards the alleviation of symptoms and improvement in quality of life. This review summarizes the recent advances in our understanding of the disease's pathogenesis and discusses the limited therapeutic options available to clinicians." @default.
- W2065514210 created "2016-06-24" @default.
- W2065514210 creator A5048327114 @default.
- W2065514210 date "1998-12-01" @default.
- W2065514210 modified "2023-09-23" @default.
- W2065514210 title "3 Pathogenesis and management of idiopathic myelofibrosis" @default.
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- W2065514210 doi "https://doi.org/10.1016/s0950-3536(98)80037-1" @default.
- W2065514210 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10640215" @default.
- W2065514210 hasPublicationYear "1998" @default.