Abstract
Acute promyelocytic leukemia (APL) is characterized by a t(15;17) which fuses the 17q retinoic acid alpha-receptor sequence to the 15q PML gene sequence. The resulting fusion product plays a role in the development and maintenance of APL, and is very rarely found in other acute myeloid leukemia (AML) subtypes. Rare complex APL genomic rearrangements have retinoic acid alpha-receptor sequence deletions. Here we report a retinoic acid alpha-receptor sequence deletion in a case of AML without differentiation. To our knowledge, this is the first example of a retinoic acid alpha-receptor sequence deletion in this AML subtype.
Original language | English (US) |
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Pages (from-to) | 407-409 |
Number of pages | 3 |
Journal | Case Reports in Oncology |
Volume | 7 |
Issue number | 2 |
DOIs | |
State | Published - Mar 6 2014 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Oncology
Keywords
- Acute myelogenous leukemia without maturation
- Acute promyelocytic leukemia
- AML-M1
- AML-M3
- Deletion
- PML/RAR?
- t(15;17)(q22;q21)