Sickle Cell Anemia and Transposition of the Great Vessels

Robert L. Hudson, Oswaldo Castro, Jerry L. Spivak, Calvin Sampson, John W. Downing

Research output: Contribution to journalArticlepeer-review

Abstract

A child with homozygous sickle cell disease and transposition of the great vessels had erythrocytosis associated with markedly increased plasma erythropoietin activity. Her clinical course was complicated by neurologic manifestations but not by recurrent sickle cell vaso-occlusive episodes. The fetal hemoglobin level which had been greater than 25% during the first two years of life gradually decreased to less than 10%. She died at 3 years of age of congestive heart failure and severe anemia. The only sickle cell painful crisis occurred during her terminal illness. It is likely that the high levels of fetal hemoglobin decreased sickling and thus allowed erythrocytosis to develop. Fetal hemoglobin may also have prevented frequent vaso-occlusive events despite the high hematocrit level.

Original languageEnglish (US)
Pages (from-to)149-151
Number of pages3
JournalAmerican Journal of Diseases of Children
Volume132
Issue number2
DOIs
StatePublished - Feb 1978

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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