Systemic mastocytosis in a child with t(8;21) acute myeloid leukemia

Pediatr Blood Cancer. 2011 Oct;57(4):684-7. doi: 10.1002/pbc.23026. Epub 2011 Feb 4.

Abstract

Mastocytosis is primarily limited to the cutaneous variant in pediatric patients. Systemic mastocytosis (SM) has been associated with t(8;21) acute myeloid leukemia (AML) in adults. We provide the first report of a child with t(8;21) AML, diagnosed with asymptomatic SM following four cycles of chemotherapy. Unlike most adults with SM/AML, she was not found to have a c-KIT (D816V) mutation. SM persisted in the bone marrow after completion of chemotherapy, and her AML relapsed 9 months off-treatment. Although she achieved a second remission, mastocytosis persists in the marrow. Pediatric patients with t(8;21) AML/SM may represent a high-risk group despite favorable cytogenetics.

Publication types

  • Case Reports

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bone Marrow / pathology
  • Cell Separation
  • Child
  • Chromosome Aberrations
  • Chromosomes, Human, Pair 8*
  • Female
  • Flow Cytometry
  • Humans
  • Immunohistochemistry
  • Immunophenotyping
  • Leukemia, Myeloid, Acute / complications*
  • Leukemia, Myeloid, Acute / drug therapy
  • Leukemia, Myeloid, Acute / genetics
  • Mastocytosis, Systemic / complications*
  • Mastocytosis, Systemic / drug therapy
  • Mastocytosis, Systemic / genetics
  • Neoplasm Recurrence, Local / drug therapy