1937
DOI: 10.1001/archderm.1937.01480010035005
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Steatocystoma Multiplex

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Cited by 11 publications
(2 citation statements)
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“…Although the pathogenesis of steatocystoma multiplex is not well understood, two main theories concerning its origin have been postulated. Some authors regard this condition as representing sebaceous or retention cysts (11,12), while others more correctly recognize it as a nevoid or hamartomatous condition (9,10). Histologic studies by Kligman and Kirschbaum (13) showed that the cysts are true tumors and a form of dermoid cyst.…”
Section: Discussionmentioning
confidence: 99%
“…Although the pathogenesis of steatocystoma multiplex is not well understood, two main theories concerning its origin have been postulated. Some authors regard this condition as representing sebaceous or retention cysts (11,12), while others more correctly recognize it as a nevoid or hamartomatous condition (9,10). Histologic studies by Kligman and Kirschbaum (13) showed that the cysts are true tumors and a form of dermoid cyst.…”
Section: Discussionmentioning
confidence: 99%
“…Steatocystoma multiplex was first described by Jamieson in 1873, and the term was coined by pringle in 1899 1 . Steatocystoma multiplex is very uncommon genetic disorder which usually begins in adolescence and early adult life 2 . The condition is inherited as an autosomal dominant in many cases 3 .…”
Section: Introductionmentioning
confidence: 99%