Table 1.

Categories of study subjects

MPDNon-MPD
BM fibrosisNo fibrosisBM fibrosisNo fibrosis
IMF (n = 15) CML (n = 5) T-cell lymphoma (n = 2) Aplastic anemia
(n = 6) 
   Lymphoma (n = 8)  
ET/IMF (n = 8) ET (n = 10) Myeloma (n = 8) Pure red cell aplasia (n = 4) 
   Myeloma (n = 5)  
CML (n = 6) PV (n = 4)  Chronic lymphocytic leukemia (n = 4)  
PV (n = 5)    
MPDNon-MPD
BM fibrosisNo fibrosisBM fibrosisNo fibrosis
IMF (n = 15) CML (n = 5) T-cell lymphoma (n = 2) Aplastic anemia
(n = 6) 
   Lymphoma (n = 8)  
ET/IMF (n = 8) ET (n = 10) Myeloma (n = 8) Pure red cell aplasia (n = 4) 
   Myeloma (n = 5)  
CML (n = 6) PV (n = 4)  Chronic lymphocytic leukemia (n = 4)  
PV (n = 5)    

Patients with PV, grouped under BM fibrosis, were transformed and then included in the study at 3-4+ fibrosis. ET/IMF, 3-4+ fibrosis indicates that patients categorized as having ET/IMF most likely had IMF with thrombocythemia that developed into ET.63 SP-IR levels in the sera of patients with ET with no evidence of reticulin fibers were less than 5 pg/mL.

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