Massive splenic infarction in an adolescent with hemoglobin S-HPFH

Donna Whyte, Bernard Forget, David H.K. Chui, Hong yuan Luo, Farzana Pashankar

Research output: Contribution to journalArticlepeer-review

2 Scopus citations


Hemoglobin sickle-hereditary persistence of fetal hemoglobin (S-HPFH) is a condition in which there is compound heterozygosity for the Hb S mutation and the HPFH deletion. These patients have no anemia, little evidence of hemolysis and generally have a benign clinical course compared to other types of sickle cell anemia. We describe a 19-year-old male with HbS-HPFH who had no history of anemia or vaso-occlusive crisis, who presented with a massive splenic infarct. We conclude that patients with HbS-HPFH can occasionally present with severe complications and require a high level of clinical suspicion for complications when presenting to the hospital.

Original languageEnglish (US)
Pages (from-to)E49-E51
JournalPediatric Blood and Cancer
Issue number7
StatePublished - Jul 2013
Externally publishedYes


  • Children
  • Sickle cell disease
  • Splenic infarction

ASJC Scopus subject areas

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


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