Association between childhood nephrotic syndrome and hemophagocytic lymphohistiocytosis

Pediatr Nephrol. 2013 Dec;28(12):2389-92. doi: 10.1007/s00467-013-2583-8. Epub 2013 Aug 15.

Abstract

Background: Hemophagocytic lymphohistiocytosis (HLH) is caused by an excessive activation of nonmalignant macrophages. Renal lesions have been described in association with, but always after, HLH diagnosis.

Case-diagnosis: We describe a previously healthy 26-month-old girl who presented originally with steroid-responsive nephrotic syndrome (NS), but after 4 months, on the first NS relapse, experienced numerous complications (many of them reported to accompany NS as single events). Clinical and laboratory signs of HLH evolved with time and led to deterioration of her condition and death, within 5 months of her original presentation.

Conclusions: To our knowledge, this is the first report of NS antedating the presentation of HLH.

Publication types

  • Case Reports

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use
  • Biopsy
  • Child, Preschool
  • Fatal Outcome
  • Female
  • Humans
  • Lymphohistiocytosis, Hemophagocytic / diagnosis
  • Lymphohistiocytosis, Hemophagocytic / etiology*
  • Multiple Organ Failure / etiology
  • Nephrotic Syndrome / complications
  • Nephrotic Syndrome / congenital*
  • Nephrotic Syndrome / diagnosis
  • Nephrotic Syndrome / drug therapy
  • Recurrence
  • Time Factors
  • Treatment Outcome

Substances

  • Adrenal Cortex Hormones

Supplementary concepts

  • Nephrotic syndrome, idiopathic, steroid-resistant