Gadolinium-associated nephrogenic systemic fibrosis in a 9-year-old boy

Clare Foss, Jeff K. Smith, Luis A Ortiz, Coral Hanevold, Loretta S Davis

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

We describe a 9-year-old boy on chronic hemodialysis who presented with hyperpigmented, tightly bound-down, indurated plaques of his bilateral lower extremities. Pertinent history included a recent series of magnetic resonance imaging tests utilizing gadolinium-based contrast media. Histopathology showed widened septae with increased fibroblasts and collagen in the subcutis consistent with nephrogenic systemic fibrosis. Nephrogenic systemic fibrosis is a unique fibrosing disorder characterized by skin thickening of the extremities and trunk, resembling that seen in systemic sclerosis. The majority of cases have been reported in dialysis or renal transplant patients. This case of nephrogenic systemic fibrosis in a young child is presented to raise awareness in the pediatric community of nephrogenic systemic fibrosis and of gadolinium contrast being a possible trigger.

Original languageEnglish (US)
Pages (from-to)579-582
Number of pages4
JournalPediatric dermatology
Volume26
Issue number5
DOIs
StatePublished - Sep 1 2009

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Nephrogenic Fibrosing Dermopathy
Gadolinium
Renal Dialysis
Systemic Scleroderma
Contrast Media
Lower Extremity
Collagen
Extremities
Fibroblasts
History
Magnetic Resonance Imaging
Pediatrics
Transplants
Skin

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Dermatology

Cite this

Gadolinium-associated nephrogenic systemic fibrosis in a 9-year-old boy. / Foss, Clare; Smith, Jeff K.; Ortiz, Luis A; Hanevold, Coral; Davis, Loretta S.

In: Pediatric dermatology, Vol. 26, No. 5, 01.09.2009, p. 579-582.

Research output: Contribution to journalArticle

Foss, Clare ; Smith, Jeff K. ; Ortiz, Luis A ; Hanevold, Coral ; Davis, Loretta S. / Gadolinium-associated nephrogenic systemic fibrosis in a 9-year-old boy. In: Pediatric dermatology. 2009 ; Vol. 26, No. 5. pp. 579-582.
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