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agnogenic myeloid metaplasia

   Also found in: Acronyms, Encyclopedia, Wikipedia 0.01 sec.
agnogenic myeloid metaplasia.
agnogenic
of unknown origin.

agnogenic 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.


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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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