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Urographic findings in homozygous sickle cell disease

Radiology
|January 1, 1978
PubMed

Insights

This study found significant renal abnormalities in 69% of patients with sickle cell disease, with calyceal clubbing and papillary necrosis being common. These findings did not correlate with symptoms or hematological features.

Area of Science:

  • Nephrology
  • Hematology
  • Radiology

Background:

  • Sickle cell disease (SCD) is a genetic blood disorder with potential systemic complications.
  • Renal involvement is a known complication of SCD, but its prevalence and specific manifestations require further elucidation.

Purpose of the Study:

  • To prospectively evaluate renal abnormalities in patients with homozygous sickle cell disease using excretion urography.
  • To investigate the correlation between urographic findings, clinical symptomatology, and hematological features.

Main Methods:

  • A prospective study involving 189 patients with homozygous sickle cell disease.
  • Excretion urography was performed to assess renal structure and function.
  • Urographic findings were analyzed for prevalence and type of abnormalities.

Main Results:

  • Renal abnormalities were detected in 69% of patients.
  • Calyceal clubbing (39%) and papillary necrosis (23%) were the most common findings.
  • No significant correlation was observed between urographic abnormalities and clinical symptoms or hematological parameters.

Conclusions:

  • Homozygous sickle cell disease frequently leads to significant renal abnormalities detectable by excretion urography.
  • Calyceal clubbing and papillary necrosis are prevalent, with increasing incidence of calyceal clubbing with age.
  • Urographic findings in SCD appear independent of disease symptomatology and hematological markers.

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