Steatocystoma multiplex

（重定向自Hereditary epidermal polycystic disease）

Steatocystoma multiplex has an autosomal dominant pattern of inheritance.

Steatocystoma multiplex, also known as epidermal polycystic disease and sebocystomatosis, is a benign, autosomal dominant congenital condition resulting in multiple cysts on a person's body.

First described by Jamieson in 1873, and coined by Pringle in 1899, steatocystoma multiplex (SM) is an uncommon disorder of the pilosebaceous unit characterized by the development of numerous sebum-containing dermal cysts. Although steatocystoma multiplex has historically been described as an autosomal dominant inherited disorder, most presenting cases are sporadic. Steatocystoma simplex is the sporadic solitary tumor counterpart to steatocystoma multiplex.

单词	Hereditary epidermal polycystic disease
释义	Hereditary epidermal polycystic disease 英语百科 Steatocystoma multiplex （重定向自Hereditary epidermal polycystic disease） Steatocystoma multiplex, also known as epidermal polycystic disease and sebocystomatosis, is a benign, autosomal dominant congenital condition resulting in multiple cysts on a person's body. First described by Jamieson in 1873, and coined by Pringle in 1899, steatocystoma multiplex (SM) is an uncommon disorder of the pilosebaceous unit characterized by the development of numerous sebum-containing dermal cysts. Although steatocystoma multiplex has historically been described as an autosomal dominant inherited disorder, most presenting cases are sporadic. Steatocystoma simplex is the sporadic solitary tumor counterpart to steatocystoma multiplex.
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