Decitabine-induced kidney thrombotic microangiopathy with glomerular crescents formation and tubular necrosis: A case report

Medicine (Baltimore). 2020 Oct 23;99(43):e22901. doi: 10.1097/MD.0000000000022901.

Abstract

Introduction: Chemotherapeutic agents of direct cell damage play a role in initiating thrombotic microangiopathy (TMA), however still being underdiagnosed. Decitabine (DAC) is a pyrimidine analogue of the nucleoside cytidine, which can lead to injury to endothelium. Biopsy-proven DAC-induced kidney injury is rare.

Patient concerns: A 47-year-old Chinese man with membranous nephropathy presented recurrent edema and acute kidney injury after a 3-day course of low dose DAC infusion because of cyclophosphamide-relating thrombocytopenia.

Diagnosis: Laboratory data revealed nephrotic syndrome, hematuria, renal glycosuria and hypokalemia with hyperchloridemia. Renal pathological findings revealed TMA with secondary glomerular crescents formation (28%), partial foot process effacement and acute tubular necrosis. A diagnosis of DAC-induced renal TMA was considered.

Interventions: As DAC had been timely discontinued before admission, the patient only received supportive treatment.

Outcomes: The patient achieved rapid remission of acute kidney injury after DAC withdrawal, and his serum creatinine further decreased to normal level after 6 months.

Conclusion: Careful monitoring of renal function especially serum creatinine should be emphasized during DAC treatment.

Publication types

  • Case Reports

MeSH terms

  • Acute Kidney Injury / etiology
  • Antimetabolites, Antineoplastic / adverse effects*
  • Conservative Treatment
  • Cyclophosphamide / adverse effects
  • Decitabine / adverse effects*
  • Glomerulonephritis, Membranous / pathology
  • Humans
  • Immunosuppressive Agents / adverse effects
  • Kidney / blood supply
  • Kidney / pathology*
  • Kidney Glomerulus / pathology*
  • Male
  • Middle Aged
  • Nephrotic Syndrome / diagnosis
  • Nephrotic Syndrome / etiology
  • Thrombocytopenia / chemically induced
  • Thrombotic Microangiopathies / chemically induced*
  • Withholding Treatment

Substances

  • Antimetabolites, Antineoplastic
  • Immunosuppressive Agents
  • Decitabine
  • Cyclophosphamide