Congenital multiple clustered 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...

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Bibliographic Details
Published in:	British journal of dermatology (1951) 2000-05, Vol.142 (5), p.1040-1043
Main Authors:	De Unamuno, P., Carames, Y., Fernandez‐Lopez, E., Hernandez‐Martin, A., Peña, C.
Format:	Article
Language:	eng
Subjects:	Adolescent Adult Biological and medical sciences Buttocks congenital dermatofibroma dermatofibroma Dermatology fibrohistiocytic tumour Histiocytoma, Benign Fibrous - congenital Histiocytoma, Benign Fibrous - pathology Histiocytoma, Benign Fibrous - surgery Humans Infant, Newborn Male Medical sciences multiple dermatofibroma Recurrence Skin Neoplasms - congenital Skin Neoplasms - pathology Skin Neoplasms - surgery Skin Transplantation Tumors of the skin and soft tissue. Premalignant lesions
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Summary:	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.
ISSN:	0007-0963 1365-2133