Acute myelogenous leukemia and glycogen storage disease 1b

Maury Pinsk, Jeffrey Burzynski, Margaret Yhap, Robert B. Fraser, Brian Cummings, Micheline Ste-Marie

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

41 Citas (Scopus)

Resumen

Glycogen storage disease 1b (GSD 1b) is caused by a deficiency of glucose-6-phosphate translocase and the intracellular accumulation of glycogen. The disease presents with failure to thrive, hepatomegaly, hypoglycemia, lactic acidosis, as well as neutropenia causing increased susceptibility to pyogenic infections. We present a case of a young woman with GSD 1b who developed acute myelogenous leukemia while on long-term granulocyte colony-stimulating factor therapy. The presence of two rare diseases in a single patient raises suspicion that GSD 1b and acute myelogenous leukemia are linked. Surveillance for acute myelogenous leukemia should become part of the long-term follow-up for GSD 1b.

Idioma originalEnglish
Páginas (desde-hasta)756-758
Número de páginas3
PublicaciónJournal of Pediatric Hematology/Oncology
Volumen24
N.º9
DOI
EstadoPublished - dic. 2002
Publicado de forma externa

ASJC Scopus Subject Areas

  • Pediatrics, Perinatology, and Child Health
  • Hematology
  • Oncology

PubMed: MeSH publication types

  • Case Reports
  • Journal Article

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