Pediatric Nephrology

, Volume 11, Issue 5, pp 556–559

Renal histopathology in fatal cases of diarrhoea-associated haemolytic uraemic syndrome

  • Carol D. Inward
  • Alec J. Howie
  • Margaret M. Fitzpatrick
  • Faro Rafaat
  • David V. Milford
  • C. Mark Taylor
  • On behalf of the Association for Pediatric Nephrology
Original article

DOI: 10.1007/s004670050337

Cite this article as:
Inward, C., Howie, A., Fitzpatrick, M. et al. Pediatr Nephrol (1997) 11: 556. doi:10.1007/s004670050337

Abstract.

 Autopsy material was examined from British children dying early in the course of haemolytic uraemic syndrome (HUS). These presented after 1983, the period in which verocytotoxin-producing Escherichia coli (VTEC) infection was confirmed as the leading cause of diarrhoea-associated (D+HUS) in the United Kingdom. Of 18 cases referred for this study, 3 were found on review to have no history of a diarrhoeal prodrome (D-HUS). In the D+ patients, the median duration from onset of diarrhoea to death was 8 days (range 4–42 days). VTEC infection was confirmed in 6 cases. All had neutrophilia at presentation (median 21, range 15–49.8 × 109/l). The 15 cases had uniform pathological features, consisting of glomerular thromboses and congested rather than ischaemic glomeruli. Arteriolar thromboses were common at the hilum of glomeruli and were sometimes also seen proximally, including in interlobular arteries. There were cortical infarcts in 5 cases with extensive thrombosis. Cases were demonstrated to have significantly greater numbers of neutrophils expressed per 100 glomeruli than controls, when counted using immunohistological stains to neutrophil elastase and CD15. This study showed uniformity of the renal changes in D+ HUS and gave further evidence of the importance of neutrophils in the pathogenesis of the disease.

Key words: Haemolytic uraemic syndromeGlomerular thrombosisArteriolar thrombosesNeutrophils

Copyright information

© IPNA - International Pediatric Nephrology Association New York, USA 1997

Authors and Affiliations

  • Carol D. Inward
    • 1
  • Alec J. Howie
    • 2
  • Margaret M. Fitzpatrick
    • 3
  • Faro Rafaat
    • 4
  • David V. Milford
    • 1
  • C. Mark Taylor
    • 1
  • On behalf of the Association for Pediatric Nephrology
  1. 1.Department of Nephrology, The Birmingham Children’s Hospital, Birmingham B16 8ET, UKGB
  2. 2.Department of Pathology, University of Birmingham, Birmingham, UKGB
  3. 3.Department of Paediatric Nephrology, St. James University Hospital, Leeds, UKGB
  4. 4.Department of Histopathology, The Birmingham Children’s Hospital, Birmingham B16 8ET, UKGB