A 9‐yr‐old boy with a 2‐yr history of Fanconi anacmia developed worsening pancytopenia that was unresponsive to oxymetholone therapy. Bone marrow was difficult to aspirate but showed the presence of megakaryoblasts. Bone marrow trephine was hypercellular with large clusters of abnormal megakaryocytes and a small population of megakaryoblasts, giving a diagnosis of megakaryoblastic leukaemia.
|Number of pages||5|
|Journal||Scandinavian Journal of Haematology|
|Publication status||Published - 1986|