| Literature DB >> 18627715 |
Vivian T Laquer1, Jashin J Wu, Joshua A Tournas, Jenny E Murase, Senait W Dyson.
Abstract
Steatocystoma multiplex (SM) is characterized by multiple dermal cysts involving the pilosebaceous glands. Although most presenting cases are sporadic, there is a rare familial syndrome involving a mutation in keratin 17 (K17) that is inherited in an autosomal dominant fashion. SM often presents concomitantly with eruptive vellus hair cysts (EHVS) and pachyonychia congenital type 2 (PC-2). We report a sporadic case of SM in a 21-year-old man.Entities:
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Year: 2008 PMID: 18627715
Source DB: PubMed Journal: Dermatol Online J ISSN: 1087-2108