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Myelofibrosis with myeloid metaplasia : Disease overview and non-transplant treatment options Best Practice & Research Clinical Haematology Vol. 19, No. 3, pp. 495–517, 2006 R2 한재준
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Classification NEJM Vol. 342 Number 17
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Clinical characteristics anemia multi-organ extramedullary hematopoiesis constitutional symptoms premature death – leukemic transformation or other complications
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The population-based incidence 1.46/100 000 (Olmsted County,MN, USA) Median age at diagnosis : 67years 0.4/100 000 (Goteborg, Sweden)
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Epidemiology : radiation observed at 18 times the expected incidence rate in survivors of Hiroshima exposed to low-level radiation radioactive contrast material Thorotrast
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Pathogenesis Stem cell derived clonal myeloproliferation Intense bone marrow stromal reaction collagen fibrosis osteosclerosis angiogenesis
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Pathogenesis 50% karyotypic abnormalities JAK2 cytoplasmic tyrosine kinase signal transduction from hematopoietic GFs acquired activating mutation Val 617 Phe – point mutation 35% in MMM
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Pathology NEJM Vol. 342 Number 17
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Pathogenesis NEJM Vol. 342 Number 17
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Pathogenesis Cytokines transforming growth factor beta-1 (TGF-b1), basic fibroblast growth factor (bFGF), platelet-derived growth factor (PDGF), vascular endothelial growth factor (VGEF), osteocalcin osteoprotegerin (OPG)
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Pathogenesis GATA-1 zinc finger transcription factor erythroid and megakaryocyte development release TGF-b1, PDGF from megakaryocyte
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Clinical manifestations
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Clinical manifestations : anemia Ineffective hematopoiesis Decreased marrow reserve Splenic sequestration Myelosuppression from cytoreductive therapy Hemolysis GI bleeding-variceal bleeding Iron, Vit B12, Folate deficiencies
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Diagnosis Reactive myelofibrosis Exposure to exogenous marrow toxins - benzene autoimmune diseases – SLE Disorders of bone matrix – osteopetrosis Non myeloid causes of reactive myelofibrosis Lymphoma Hairy cell leukemia Metastatic cancer
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Prognosis
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Management - anemia
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Management - Epo a response rate of 33% with drug doses of up to 600 units/kg/week. (Rodriguez et al) endogenous serum Epo levels <125 mU/mL highest likelihood of response an overall response rate of 45% in 20 MMM patients treated with 30 000 units/week. (Cervantes et al) Epo treatment should be restricted to patients with anemia and inadequate Epo levels
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Clinical trials of thalidomide
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Medical therapy for reduction of myeloproliferation
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Mayo clinic experience of splenectomy
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Radiotherapy for palliation
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