Congenital Infantile Fibrosarcoma Associated With a Lipofibromatosis-Like Component: One Train May Be Hiding Another

Am J Dermatopathol. 2017 Jun;39(6):463-467. doi: 10.1097/DAD.0000000000000696.

Abstract

Congenital infantile fibrosarcoma (CIFS) is a soft tissue sarcoma of infants mainly involving lower extremities and usually developing during the first year of life. At another end of the spectrum of pediatric fibroblastic lesions, lipofibromatosis is a rare benign infiltrative soft tissue tumor that affects children. The authors report in this study a particular presentation with a CIFS surrounded by lipofibromatosis-like areas. The presence of a surrounding benign tumor confused and delayed CIFS diagnosis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Biopsy
  • Delayed Diagnosis
  • Female
  • Fibroma / congenital
  • Fibroma / pathology*
  • Fibroma / surgery
  • Fibrosarcoma / congenital
  • Fibrosarcoma / pathology*
  • Fibrosarcoma / surgery
  • Humans
  • Infant, Newborn
  • Lipoma / congenital
  • Lipoma / pathology*
  • Lipoma / surgery
  • Magnetic Resonance Imaging
  • Neoplasms, Complex and Mixed / congenital
  • Neoplasms, Complex and Mixed / pathology*
  • Neoplasms, Complex and Mixed / surgery
  • Predictive Value of Tests
  • Pregnancy
  • Prenatal Diagnosis
  • Soft Tissue Neoplasms / congenital
  • Soft Tissue Neoplasms / pathology*
  • Soft Tissue Neoplasms / surgery
  • Tomography, X-Ray Computed
  • Tumor Burden