AML-M4; acute myelomonocytic leukemia
Jump to navigation
Jump to search
Pathology
- myelocytic & monocytic differentiation evident
- myeloid elements resemble M2; peripheral monocytosis.
Genetics
- chromosomal translocation t(5;17)(q33;p11.2) involving SPECC1 with PDGFRB may be a cause of juvenile myelomonocytic leukemia
- chromosomal translocation t(5;11)(q31;q23) involving ARHGAP26 with MLL has been found in a case of juvenile myelomonocytic leukemia
More general terms
More specific terms
Additional terms
References
- ↑ Cotran et al Robbins Pathologic Basis of Disease, W.B. Saunders Co, Philadelphia, PA 1989 pg 726
- ↑ Liu et al, Fusion between transcription factor CBF beta/PEB2 beta and a myosin heavy chain in acute myeloid leukemia. Science 261:1041 1993 PMID: https://www.ncbi.nlm.nih.gov/pubmed/8351518
- ↑ Mihova D Leukemia - Acute AML not otherwise categorized Acute myelomonocytic leukemia (FAB AML M4) Pathology Outlines http://www.pathologyoutlines.com/topic/leukemiaM4.html
Patient information
acute myelomonocytic leukemia patient information