Affiliations 

  • 1 Universiti Putra Malaysia, Faculty of Medicine and Health Sciences, Department of Paediatrics, Selangor, Malaysia. t_puiling@upm.edu.my
  • 2 University Putra Malaysia, Faculty of Medicine and Health Sciences, Department of Medicine, Selangor, Malaysia
  • 3 University Putra Malaysia, Faculty of Medicine and Health Sciences, Department of Pathology, Selangor, Malaysia
Med J Malaysia, 2020 07;75(4):436-438.
PMID: 32724011

Abstract

Henoch-Schonlein Purpura (HSP) or anaphylactoid purpura, currently named IgA vasculitis is the most common form of systemic vasculitis in children. In adults and young infants, HSP tends to have atypical presentations with higher rates of severe gastrointestinal problems and delayed renal complications. While hypertension is a known complication of HSP nephritis, it is rarely seen in individuals with normal renal function and urinary findings. We report a case of a 7-year-old boy with HSP, who presented with abdominal pain and severe hypertension without other features of glomerulonephritis.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.