Answers are grounded in this paper and cite their sources.
A 50-year-old patient demonstrated an acute atypical variant of myelofibrosis characterized by diffuse marrow fibrosis, peripheral myeloblastosis, normal erythrocyte morphology, lack of massive splenomegaly, and a rapidly fatal course. Although this variant is rare in comparison with other myeloproliferative disorders, it deserves recognition. We favor the designation "acute myelofibrosis" for this entity.
No takes yet. Share an insight, caveat, or question.
Bergsman et al. (1971) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: