A case of IgA-related enteropathy complicated with gastrointestinal bleeding and progressive IgA nephropathy: a possible variant Henoch-Schönlein purpura?

Intern Med. 2010;49(16):1755-61. doi: 10.2169/internalmedicine.49.3678. Epub 2010 Aug 13.

Abstract

Here, we report an adult patient with IgA-related enteropathy complicated with massive intestinal bleeding and acute renal failure, but without skin lesions. Surgical resection of the small intestine and steroid pulse therapy was performed. Histopathology revealed significant deposition of IgA and C3 in the small vessels of the intestine and the kidney mesangium. Although skin purpura was absent, the histopathology and clinical manifestations suggested that the pathophysiology was similar to Henoch-Schönlein purpura (HSP), implying IgA-related enteropathy as a subclass of HSP. Retrospective analysis indicates that terminal ileum lesions may be a poor prognostic indicator.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Diagnosis, Differential
  • Disease Progression*
  • Fatal Outcome
  • Gastrointestinal Hemorrhage / complications
  • Gastrointestinal Hemorrhage / diagnosis*
  • Glomerulonephritis, IGA / complications
  • Glomerulonephritis, IGA / diagnosis*
  • Humans
  • IgA Vasculitis / complications
  • IgA Vasculitis / diagnosis*
  • Immunoglobulin A* / adverse effects
  • Male
  • Middle Aged
  • Retrospective Studies

Substances

  • Immunoglobulin A