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Congenital Multiple Clustered Dermatofibroma in a 12‐Year‐Old Girl
Authors:JUSTIN FINCH M.D.  ADRIENNE BERKE M.D.  MEAGEN McCUSKER M.D.  MARY WU CHANG M.D.
Affiliation:Department of Dermatology, School of Medicine, University of Connecticut, Farmington, Connecticut
Abstract:Abstract: Congenital multiple clustered dermatofibroma (MCDF) is a rare, idiopathic, benign tumor presenting at birth as an asymptomatic hyperpigmented patch that is stable until puberty, at which time it enlarges and develops papules. Ultimately, MCDF appears to follow a stable, benign course. We present a case of a 12‐year‐old girl with congenital MCDF. To our knowledge, this is only the third reported case of congenital presentation of MCDF and the only case featuring atrophoderma‐like depression.
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