Acral subcutaneous steatocystoma multiplex: A distinct subtype of the disease?

ABSTRACT Steatocystoma multiplex (SM) is a hamartomatous malformation of the pilosebaceous duct consisting of dermal cysts filled with a sebum‐like material. SM lesions are typically located in areas with sebaceous follicles, although atypical presentations involving sites lacking sebaceous follicle...

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Veröffentlicht in:Australasian journal of dermatology 2012-08, Vol.53 (3), p.198-201
Hauptverfasser: Marzano, Angelo V, Tavecchio, Simona, Balice, Ylenia, Polloni, Ilaria, Veraldi, Stefano
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container_title Australasian journal of dermatology
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creator Marzano, Angelo V
Tavecchio, Simona
Balice, Ylenia
Polloni, Ilaria
Veraldi, Stefano
description ABSTRACT Steatocystoma multiplex (SM) is a hamartomatous malformation of the pilosebaceous duct consisting of dermal cysts filled with a sebum‐like material. SM lesions are typically located in areas with sebaceous follicles, although atypical presentations involving sites lacking sebaceous follicles have exceptionally been described. We reviewed retrospectively a series of 32 histologically diagnosed SM observed in our department in the period 2006–2010, evaluating the kinds of lesions and their locations, and family history of SM and associated disorders, to focus on the clinical features of the acral subcutaneous variety of SM and to estimate its prevalence. We found five patients (four women and one man) with asymptomatic deep, skin‐colored nodules on the flexor surfaces of distal upper extremities with a mean age at diagnosis and at disease onset of 32.5 and 26 years, respectively. The prevalence was 15%. All five cases were sporadic. The male patient had eruptive syringomas as an associated condition, together with a family history of this tumour. Acral subcutaneous SM may represent a distinct disease variety by virtue of its distinctive clinical features. Dermatologists should be aware of this form, which has to be included in the wide panel of diseases involving subcutaneous tissue.
doi_str_mv 10.1111/j.1440-0960.2011.00851.x
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General aspects ; steatocystoma ; Steatocystoma Multiplex - complications ; Steatocystoma Multiplex - genetics ; Steatocystoma Multiplex - pathology ; Sweat Gland Neoplasms - complications ; Syringoma - complications ; Tumors of the skin and soft tissue. Premalignant lesions ; Young Adult</subject><ispartof>Australasian journal of dermatology, 2012-08, Vol.53 (3), p.198-201</ispartof><rights>2012 The Authors. Australasian Journal of Dermatology © 2012 The Australasian College of Dermatologists</rights><rights>2015 INIST-CNRS</rights><rights>2012 The Authors. 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SM lesions are typically located in areas with sebaceous follicles, although atypical presentations involving sites lacking sebaceous follicles have exceptionally been described. We reviewed retrospectively a series of 32 histologically diagnosed SM observed in our department in the period 2006–2010, evaluating the kinds of lesions and their locations, and family history of SM and associated disorders, to focus on the clinical features of the acral subcutaneous variety of SM and to estimate its prevalence. We found five patients (four women and one man) with asymptomatic deep, skin‐colored nodules on the flexor surfaces of distal upper extremities with a mean age at diagnosis and at disease onset of 32.5 and 26 years, respectively. The prevalence was 15%. All five cases were sporadic. The male patient had eruptive syringomas as an associated condition, together with a family history of this tumour. Acral subcutaneous SM may represent a distinct disease variety by virtue of its distinctive clinical features. Dermatologists should be aware of this form, which has to be included in the wide panel of diseases involving subcutaneous tissue.</description><subject>acral subcutaneous steatocystoma multiplex</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Dermatology</subject><subject>eruptive syringomas</subject><subject>Female</subject><subject>Forearm</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Skin involvement in other diseases. Miscellaneous. General aspects</subject><subject>steatocystoma</subject><subject>Steatocystoma Multiplex - complications</subject><subject>Steatocystoma Multiplex - genetics</subject><subject>Steatocystoma Multiplex - pathology</subject><subject>Sweat Gland Neoplasms - complications</subject><subject>Syringoma - complications</subject><subject>Tumors of the skin and soft tissue. 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Miscellaneous. General aspects</topic><topic>steatocystoma</topic><topic>Steatocystoma Multiplex - complications</topic><topic>Steatocystoma Multiplex - genetics</topic><topic>Steatocystoma Multiplex - pathology</topic><topic>Sweat Gland Neoplasms - complications</topic><topic>Syringoma - complications</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marzano, Angelo V</creatorcontrib><creatorcontrib>Tavecchio, Simona</creatorcontrib><creatorcontrib>Balice, Ylenia</creatorcontrib><creatorcontrib>Polloni, Ilaria</creatorcontrib><creatorcontrib>Veraldi, Stefano</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Australasian journal of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marzano, Angelo V</au><au>Tavecchio, Simona</au><au>Balice, Ylenia</au><au>Polloni, Ilaria</au><au>Veraldi, Stefano</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acral subcutaneous steatocystoma multiplex: A distinct subtype of the disease?</atitle><jtitle>Australasian journal of dermatology</jtitle><addtitle>Australas J Dermatol</addtitle><date>2012-08</date><risdate>2012</risdate><volume>53</volume><issue>3</issue><spage>198</spage><epage>201</epage><pages>198-201</pages><issn>0004-8380</issn><eissn>1440-0960</eissn><coden>AJDEBP</coden><abstract>ABSTRACT Steatocystoma multiplex (SM) is a hamartomatous malformation of the pilosebaceous duct consisting of dermal cysts filled with a sebum‐like material. SM lesions are typically located in areas with sebaceous follicles, although atypical presentations involving sites lacking sebaceous follicles have exceptionally been described. We reviewed retrospectively a series of 32 histologically diagnosed SM observed in our department in the period 2006–2010, evaluating the kinds of lesions and their locations, and family history of SM and associated disorders, to focus on the clinical features of the acral subcutaneous variety of SM and to estimate its prevalence. We found five patients (four women and one man) with asymptomatic deep, skin‐colored nodules on the flexor surfaces of distal upper extremities with a mean age at diagnosis and at disease onset of 32.5 and 26 years, respectively. The prevalence was 15%. All five cases were sporadic. The male patient had eruptive syringomas as an associated condition, together with a family history of this tumour. 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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects acral subcutaneous steatocystoma multiplex
Adolescent
Adult
Biological and medical sciences
Dermatology
eruptive syringomas
Female
Forearm
Humans
Male
Medical sciences
Middle Aged
Skin involvement in other diseases. Miscellaneous. General aspects
steatocystoma
Steatocystoma Multiplex - complications
Steatocystoma Multiplex - genetics
Steatocystoma Multiplex - pathology
Sweat Gland Neoplasms - complications
Syringoma - complications
Tumors of the skin and soft tissue. Premalignant lesions
Young Adult
title Acral subcutaneous steatocystoma multiplex: A distinct subtype of the disease?
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