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Abstract

Henoch-Schonlein purpura is the most common vasculitis in childhood with the pathogenesis of immunoglobulin A deposition in small-vessel wall. As the end-organ vasculature involved, this disease is characterized by palpable purpura, abdominal pain, arthritis, and renal disease. Renal involvement may present with isolated haematuria and/or proteinuria from mild to severe as nephrotic levels. Membranoproliferative glomerulonephritis is the most common cause of chronic glomerulonephritis in older children and young adults and also one of the major causes of nephrotic syndrome. In this case, we reported the concurrent of leukocytoclastic glomerulonephritis. Key Membranoproliferative Glomerulonephritis, Nephrotic Syndrome

Keywords

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Lökositoklastik Vaskulit ve Membrano-proliferatif Glomerulonefrit Birlikteliği: Bir Olgu Sunumu

Abstract

Henoch-Schonlein duvarında immünglobulin A birikimi ile karakterize çocukluk çağının en sık rastlanan vaskülitidir. Hedef organda damarsal yapının tutulması sonucu palpe edilebilen purpura, karın ağrısı, artrit ve böbrek hastalığı görülür. Böbrek tutulumu, izole hematüri ve/veya hafif düzeyden nefrotik düzeylerdeki oranlara varan Membranoproliferatif glomerulonefrit, büyük çocuklarda ve genç erişkinlerde kronik glomerulonefritin en sık sebebidir ve aynı zamanda nefrotik sendromun en önemli sebeplerinden biridir. Bu vakada, lökositoklastik vaskülit ile membranoproliferatif glomerulonefrit birlikteliği sunulmuştur

Keywords

• Anahtar

References

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