Mild Splenic Sequestration Crises in Sickle-Hemoglobin C Disease

J. Andrews, G. R. Buchanan

Research output: Contribution to journalArticlepeer-review

7 Scopus citations


Acute splenic sequestration crisis (ASSC), a common complication in homozygous sickle cell anemia, has been described infrequently in sickle-hemoglobin C (SC) disease in the absence of high altitude exposure. In this report, we describe three children with hemoglobin SC disease who developed episodes of ASSC that were milder than those generally described in sickle cell anemia. In one patient, an antecedent triggering event was not recognized. The other two children may have had a predisposing cause for massive intrasplenic sickling in that one had an associated mononucleosis syndrome and the other an episode of hypovolemic shock following severe epistaxis. ASSC may occur in patients with SC disease and does not necessarily require a hypoxic trigger associated with high altitudes.

Original languageEnglish (US)
Pages (from-to)354-355
Number of pages2
JournalClinical Pediatrics
Issue number6
StatePublished - Jun 1984

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health


Dive into the research topics of 'Mild Splenic Sequestration Crises in Sickle-Hemoglobin C Disease'. Together they form a unique fingerprint.

Cite this