Low serum C3, leukopenia, and thrombocytopenia: Unusual features of Henoch-Schonlein purpura

I. Krause*, B. Z. Garty, M. Davidovits, R. Cleper, H. Tamary, E. Rosenmann, B. Eisenstein

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Henoch-Schonlein purpura (HSP) affects predominantly the skin, joints, gastrointestinal tract and kidney. Although the pathogenesis is probably of immune origin and complement activation is thought to play a role, laboratory findings including the serum level of the complement components are usually normal. We present a patient with a severe form of HSP nephritis who had unusual laboratory findings of a low level of C3, mild leukopenia and thrombocytopenia. These findings may further support the importance of complement activation in the pathogenesis of HSP.

Original languageEnglish
Pages (from-to)906-909
Number of pages4
JournalEuropean Journal of Pediatrics
Volume158
Issue number11
DOIs
StatePublished - 1999

Keywords

  • C3
  • Henoch-Schonlein purpura
  • Hypocomplementemia
  • Nephritis

Fingerprint

Dive into the research topics of 'Low serum C3, leukopenia, and thrombocytopenia: Unusual features of Henoch-Schonlein purpura'. Together they form a unique fingerprint.

Cite this