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agnogenic myeloid metaplasia |
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agnogenic myeloid metaplasia. See myeloid metaplasia. agnogenic of unknown origin. agnogenic myeloid metaplasia see myeloid metaplasia. agnogenic myeloid metaplasia Myelofibrosis with myeloid metaplasia Hematology A chronic progressive condition–panmyelosis and variable BM fibrosis, massive splenomegaly 2º to extramedullary hematopoiesis and leukoerythroblastic
anemia with dysmorphic RBCs, circulating normoblasts, immature WBCs, atypical platelets Clinical Pts are often > age 50, insidious weight loss, anemia, abdominal discomfort due to splenomegaly, often with hepatomegaly; 80% have nonspecific
chromosome defects Diagnosis BM Bx Management No specific therapy; packed RBCs for anemia, androgens may ↓ transfusion requirements, but are poorly tolerated in ♀; recombinant erythropoietin Prognosis Survival ± 5 yrs, often →
acute leukemia. See Pseudonym syndrome. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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| ? Mentioned in | ? References in periodicals archive | ||
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| Ten patients each with either agnogenic myeloid metaplasia,
polycythemia vera, or primary thrombocytothemia will be given low dose
oral interferon alpha daily for 6-12 months as a treatment to relieve
the signs and symptoms associated with these disorders. |
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