Sternal cupping: a new finding in childhood sickle cell anemia

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Insights

Discrete sternal cupping is a newly identified bone abnormality in children with sickle cell anemia (SCA) and sickle cell-hemoglobin C disease. Radiologists should recognize this benign finding to avoid misdiagnosis.

Area of Science:

  • Pediatric Hematology
  • Pediatric Radiology
  • Skeletal Imaging

Background:

  • Sickle cell anemia (SCA) is a genetic blood disorder associated with various bone abnormalities.
  • Discrete sternal cupping has not been previously documented in pediatric patients with SCA.

Purpose of the Study:

  • To report the novel finding of discrete sternal cupping in children with SCA and related hemoglobinopathies.
  • To determine the prevalence of sternal cupping in this population.
  • To inform radiologists about this benign finding.

Main Methods:

  • Retrospective analysis of imaging studies in children diagnosed with sickle cell anemia or sickle cell-hemoglobin C disease.
  • Evaluation for the presence and characteristics of sternal cupping.

Main Results:

  • Discrete sternal cupping was observed in 8% of children with homozygous SCA.
  • The phenomenon was present in 10.6% of children with sickle cell-hemoglobin C disease.
  • Sternal cupping was a temporary finding with minimal clinical significance.

Conclusions:

  • Discrete sternal cupping should be recognized as part of the spectrum of osseous abnormalities in sickle cell disease.
  • Awareness of this finding can prevent misinterpretation as a more severe sternal pathology.

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