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Keywords:

  • congenital dermatofibroma;
  • dermatofibroma;
  • fibrohistiocytic tumour;
  • multiple dermatofibroma

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.