Abstract：
:A 17-year-old white boy with no underlying connective tissue disorders presented with flat-topped annular plaques, with slight central atrophy on the bilateral neck. Results from histopathology revealed changes consistent with elastosis perforans serpiginosa (EPS). The idiopathic form of EPS occurs rarely in children. We report a patient with this rare pediatric diagnosis and review the literature.
journal_name
Cutisjournal_title
Cutisauthors
Wu JJ,Wagner AMsubject
Has Abstractpub_date
2002-06-01 00:00:00pages
423-5issue
6eissn
0011-4162issn
2326-6929journal_volume
69pub_type
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