Abstract
We report a patient with multiple apocrine hidrocystoma (cystadenoma) which was characterized by bilateral distribution of the lesions on the eyelids. The disease is benign, but it may be a marker of two rare inherited disorders, the Schopf-Schulz-Passarge syndrome and a peculiar form of focal dermal hypoplasia.
Original language | English |
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Pages (from-to) | 642-645 |
Number of pages | 4 |
Journal | British Journal of Dermatology |
Volume | 137 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1997 |
ASJC Scopus subject areas
- Dermatology