[The pathophysiology, clinical signs and therapy of urate nephropathy]

Orv Hetil. 2007 Apr 22;148(16):745-8. doi: 10.1556/OH.2007.27989.
[Article in Hungarian]

Abstract

Tumor lysis syndrome is an oncologic emergency that is characterized by severe electrolyte abnormalities. The syndrome occurs in patients with lymphoproliferative malignancies, most often after chemotherapy, but also spontaneously. The pathophysiology involves tumor cell lysis resulting in the release of potassium, phosphate and uric acid. The deposition of uric acid and calcium phosphate crystals in the renal tubules may lead to acute renal failure. The treatment consists in hydration, correction of the acidosis and hyperkalemia, use of allopurinol and recombinant urate oxidase (rasburicase) for preventing urate nephropathy and haemodialysis. The authors report a case of a patient with acute myeloid leukemia, who developed severe tumor lysis syndrome after chemotherapy.

Publication types

  • Review

MeSH terms

  • Acidosis / etiology
  • Acidosis / therapy
  • Acute Kidney Injury* / complications
  • Acute Kidney Injury* / diagnosis
  • Acute Kidney Injury* / metabolism
  • Acute Kidney Injury* / physiopathology
  • Acute Kidney Injury* / therapy
  • Allopurinol / administration & dosage
  • Fluid Therapy
  • Humans
  • Hyperkalemia / etiology
  • Hyperkalemia / therapy
  • Kidney Tubules / metabolism*
  • Recombinant Proteins / administration & dosage
  • Renal Dialysis
  • Tumor Lysis Syndrome / complications
  • Tumor Lysis Syndrome / metabolism
  • Urate Oxidase / administration & dosage
  • Uric Acid / metabolism*

Substances

  • Recombinant Proteins
  • rasburicase
  • Uric Acid
  • Allopurinol
  • Urate Oxidase