Unsuspected glucose-6-phosphate dehydrogenase deficiency presenting as symptomatic methemoglobinemia with severe hemolysis after fava bean ingestion in a 6-year-old boy

Int J Hematol. 2011 May;93(5):664-666. doi: 10.1007/s12185-011-0827-6. Epub 2011 Apr 12.

Abstract

We report the occurrence of symptomatic methemoglobinemia in a previously healthy boy, who presented with severe acute hemolysis after fava bean ingestion. The methemoglobinemia revealed a previously unrecognized glucose-6-phosphate dehydrogenase (G6PD) deficiency. We discuss the pathophysiology of severe methemoglobinemia when associated with acute hemolysis, favism, and the common African G6PD A-variant [G6PD, VAL68MET, ASN126ASP]. In conclusion, screening for G6PD deficiency must be considered in symptomatic methemoglobinemia, especially in young boys, when associated with intravascular hemolysis.

Publication types

  • Case Reports

MeSH terms

  • Algeria
  • Child
  • Eating
  • Favism / complications
  • Favism / diagnosis*
  • Favism / physiopathology
  • Glucosephosphate Dehydrogenase / blood*
  • Glucosephosphate Dehydrogenase / genetics
  • Glucosephosphate Dehydrogenase Deficiency / complications
  • Glucosephosphate Dehydrogenase Deficiency / diagnosis*
  • Glucosephosphate Dehydrogenase Deficiency / physiopathology
  • Hemolysis / drug effects
  • Hemolytic Agents / administration & dosage
  • Hemolytic Agents / adverse effects
  • Humans
  • Male
  • Methemoglobinemia / complications
  • Methemoglobinemia / diagnosis*
  • Methemoglobinemia / physiopathology
  • Mutation
  • Vicia faba / adverse effects

Substances

  • Hemolytic Agents
  • Glucosephosphate Dehydrogenase