Table 1.
Pathology | Sites of EMH | Lineage | Number of Cases | Human/Animal Studies | References |
---|---|---|---|---|---|
Primary myelofibrosis | Spleen liver |
5 patients | Human | [22] | |
Secondary myelofibrosis after essential thrombocythemia | Spleen | 1 patient | Human | [22] | |
Primary myelofibrosis | Spleen | Malignant primitive HPCs (PB CD34+) |
8 patients | Human | [23] |
Allograft liver transplant | Liver | 27 patients | [30] | ||
Acute promyelocytic leukemia (APL) | Central nervous system, skin, lung, | Leukemia cells | 21 patients | Human | [31] |
Chronic myelogenous leukemia | Stomach | Case reports | Human | [3,4,32] | |
Thalassemia | N/A | 10 patients | Human | [33] | |
Agnogenic myeloid metaplasia | Lung | 2 | Human | [34] | |
Primary myelofibrosis (MMM) | Spleen | Granulocyte infiltration | 213 patients (MMM) | Human | [35] |
Myelofibrosis with myeloid metaplasia (MMM) with thalidomide therapy |
Liver/spleen Pericardium |
Red blood cells Granulocytic precursors |
1 of 7 patients | Human | [36] |
Chronic myeloproliferative diseases | Spleen | JAK2(V617F) | 15 patients 47 patients |
Human Human |
[37] [38] |
Experimental spondylarthritis | Spleen Inflamed joints |
Myelopoiesis | 39 mice (13 mice/group) | Animal/experimental | [25] |
Inflammation | Spleen, liver, other sites | Megakaryopoiesis | N/A | Animal | [28] |
Experimental mutations in the SETD1B gene; | Spleen | Myeloid and lymphoid | N/A | Animal | [39] |
Acute myeloid leukemia | Spleen | N/A | Animal | [40] | |
Experimental overexpression of Tlx1 | Spleen | N/A | Animal | [29] | |
Experimental Dnmt3a loss of function | Spleen, liver | HSC | 18 mice | Animal | [41] |