“…It is most commonly associated with myelofibrosis and other conditions in which there is a disruption of normal haemopoiesis in the bone marrow. It is also seen as a result of haemolytic anaemias such as hereditary spherocytosis, thalassaemia and sickle cell disease 5,7 . EMH occurs most frequently in the spleen, liver and lymph nodes, however it has also been described in the thyroid, endometrium, central nervous system, subcutaneous tissue, pleura, retroperitoneum, mediastinum, breast and kidney 1–7,9,10,13–21 .…”