Congenital multiple clustered dermatofibroma

Br J Dermatol. 2000 May;142(5):1040-3. doi: 10.1046/j.1365-2133.2000.03494.x.

Abstract

Multiple clustered dermatofibroma (MCD) is a rare tumour which usually appears during the first and second decades of life. We report a man in whom the MCD was congenital, although during the first few years of his second decade it extended to involve a broad zone on the left hip, gluteal region and upper thigh.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Buttocks
  • Histiocytoma, Benign Fibrous / congenital*
  • Histiocytoma, Benign Fibrous / pathology
  • Histiocytoma, Benign Fibrous / surgery
  • Humans
  • Infant, Newborn
  • Male
  • Recurrence
  • Skin Neoplasms / congenital*
  • Skin Neoplasms / pathology
  • Skin Neoplasms / surgery
  • Skin Transplantation