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.
|Number of pages||4|
|Journal||British Journal of Dermatology|
|Publication status||Published - 1997|
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