Journal of Hematology, ISSN 1927-1212 print, 1927-1220 online, Open Access
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Case Report

Volume 4, Number 1, March 2015, pages 148-150

Acquired β-Thalassemia as an Etiology of Microcytic Anemia in Primary Myelofibrosis


Figure 1.
Figure 1. Bone marrow biopsy at diagnosis. The bone marrow was hypercellular with marked fibrosis of grade MF-3 (A, low power view, silver stain) and increased number of megakaryocytes with dysplastic features (arrows) (B, high power view, hematoxylin-eosin stain).