英文摘要 |
A 48-year-old male had experienced acute-onset epigastragia, palpable purpura, ischemic bowel, and oligoarthritis 12 years ago. Panendoscopy showed peptic ulcer disease. Recovery was complete after a three-week high dose corticosteroid (prednisolone 60 mg/day) regimen in a diagnosis of Henoch-Schonlein purpura (HSP). The present recurrence of the symptoms and signs prompted his admittance to our hospital last year. Laboratory analyses revealed elevated levels of serum immunoglobulin A (IgA), C-reactive protein (CRP), leukocytosis and thrombocytosis. Screening was negative for autoantibodies. Panendoscopy showed duodenal ulcers related to the presence of Helicobacter pylori (H. pylori). Skin biopsy revealed leukocytoclastic vasculitis. Although high dose corticosteroids (prednisolone 60 mg/day) was given, rapidly progressive glomerulonephritis with nephrotic-level proteinuria, microscopic hematuria, pyuria, hypoalbuminemia, bilateral edema on the lower legs and hypertension subsequently occurred. Renal biopsy showed endocapillary and extracapillary proliferative glomerulonephritis with cellular crescents formation involving more than 50% of the glomeruli. Immunofluorescence and electron microscopy demonstrated IgA deposition mainly in the mesangial matrix. Pulsed intravenous administration of cyclophosphamide (800 mg/month) and prednisolone (20 mg/day) ultimately controlled the disease. |