“…As is the case with physiologic EMH in the fetus, the liver and spleen are the usual sites of pathologic EMH. However, nonhepatosplenic EMH (NHS-EMH) has been reported in a myriad of other tissues and organs, including the mediastinum, 1 central nervous system, 2 peripheral nerves, 3 middle ear, 4 pancreas, 5,6 urethra, 7 pharynx, 8 pleura and lungs, 5,9,10 pericardium, 11 heart, 5,12 gastrointestinal tract, 5,13 peritoneum, 5,14 thyroid gland, 15 skin, 5,16 kidney, 5,17,18 adrenal gland, 5 prostate gland, 19 breast, 20 epididymis, 5 and endometrium. 21 Al-though NHS-EMH is often associated with myelofibrosis with myeloid metaplasia (MMM) 17 or thalassemia, 22 it can also accompany other disorders, including hereditary spherocytosis, [23][24][25] sickle cell anemia, 26,27 congenital dyserythropoietic anemia, 28 immune thrombocytopenic purpura, 29 chronic myeloid leukemia, 11,30 polycythemia vera, 31,32 myelodysplastic syndrome, 33 Paget disease, 34 osteopetrosis, 35 and Gaucher disease, 36 and treatm...…”