A "silent" course of normotensive scleroderma renal crisis: case report and review of the literature


Akoglu H., Atilgan G. K. , Ozturk R., Yenigun E. C. , IŞIK GÖNÜL İ. , Odabas A. R.

RHEUMATOLOGY INTERNATIONAL, vol.29, no.10, pp.1223-1229, 2009 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Review
  • Volume: 29 Issue: 10
  • Publication Date: 2009
  • Doi Number: 10.1007/s00296-008-0807-1
  • Title of Journal : RHEUMATOLOGY INTERNATIONAL
  • Page Numbers: pp.1223-1229

Abstract

Scleroderma renal crisis (SRC) is a complication of systemic sclerosis characterized by the sudden onset of accelerated arterial hypertension, followed by progressive renal failure. Rarely, patients with SRC may be normotensive on presentation. These patients have poorer prognosis and higher mortality rates than those with hypertensive SRC. This is partly explained by the insidious course of normotensive SRC leading to delayed diagnosis and treatment. Normotensive patients also seem to be less responsive to current treatment modalities. Since available data on etiology, pathogenesis, and risk factors of the disease are inadequate, no effective therapy has been established to date. We report a patient with diffuse cutaneous scleroderma who developed SRC during his hospitalization. The patient remained normotensive and had an insidious course until oliguria and signs of hypervolemia occurred. Etiology, pathogenesis, risk factors, diagnosis, treatment modalities and prognosis of normotensive SRC are also discussed through previously published reports.