Acute myelogenous leukemia without maturation with a retinoic alpha-receptor deletion: A case report

Christopher Trosclair, Maressa Pollen, Gerald Capraro, James Cotelingam, Rodney E. Shackelford

Research output: Contribution to journalArticlepeer-review

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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 languageEnglish (US)
Pages (from-to)407-409
Number of pages3
JournalCase Reports in Oncology
Volume7
Issue number2
DOIs
StatePublished - Mar 6 2014
Externally publishedYes

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)

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