Palatal steatocystoma simplex—a rare oral finding at an even rarer location
ABSTRACT Steatocystoma is a rare, benign cyst that mostly originates from a dermal sebaceous gland. It can be divided into steatocystoma multiplex—with multiple locations—and steatocystoma simplex occurring at a single site. The lesion is mostly located on the skin but can be found on other location...
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Published in | Journal of surgical case reports Vol. 2020; no. 10 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Oxford University Press
01.10.2020
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Abstract | ABSTRACT
Steatocystoma is a rare, benign cyst that mostly originates from a dermal sebaceous gland. It can be divided into steatocystoma multiplex—with multiple locations—and steatocystoma simplex occurring at a single site. The lesion is mostly located on the skin but can be found on other locations as well. This is the first case report of steatocystoma simplex that was found in the palate of a 37-year-old male. After resection with small safety margins and local wound dressing, no recurrence was detected during a follow-up of 1.5 years. |
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AbstractList | Steatocystoma is a rare, benign cyst that mostly originates from a dermal sebaceous gland. It can be divided into steatocystoma multiplex—with multiple locations—and steatocystoma simplex occurring at a single site. The lesion is mostly located on the skin but can be found on other locations as well. This is the first case report of steatocystoma simplex that was found in the palate of a 37-year-old male. After resection with small safety margins and local wound dressing, no recurrence was detected during a follow-up of 1.5 years. ABSTRACT Steatocystoma is a rare, benign cyst that mostly originates from a dermal sebaceous gland. It can be divided into steatocystoma multiplex—with multiple locations—and steatocystoma simplex occurring at a single site. The lesion is mostly located on the skin but can be found on other locations as well. This is the first case report of steatocystoma simplex that was found in the palate of a 37-year-old male. After resection with small safety margins and local wound dressing, no recurrence was detected during a follow-up of 1.5 years. |
Author | Kaya, Sebahat Zimmer, Stefanie Kämmerer, Peer Wolfgang |
Author_xml | – sequence: 1 givenname: Sebahat surname: Kaya fullname: Kaya, Sebahat – sequence: 2 givenname: Stefanie surname: Zimmer fullname: Zimmer, Stefanie – sequence: 3 givenname: Peer Wolfgang surname: Kämmerer fullname: Kämmerer, Peer Wolfgang email: peer.kaemmerer@unimedizin-mainz.de |
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Cites_doi | 10.1016/j.jdermsci.2007.07.003 10.1159/000488584 10.1111/j.1346-8138.2002.tb00238.x 10.1016/0030-4220(88)90383-0 10.4103/0366-6999.174493 10.1097/SAP.0000000000000826 10.1046/j.1365-2133.1998.02413.x |
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References | Cho (2020100910342447300_ref4) 2002; 29 Kamra (2020100910342447300_ref6) 2013; 7 Georgakopoulos (2020100910342447300_ref9) 2018; 64 Liao (2020100910342447300_ref5) 2007; 48 Sharma (2020100910342447300_ref2) 2018; 5 Covello (2020100910342447300_ref1) 1998; 139 Gargya (2020100910342447300_ref8) 2017; 78 Olsen (2020100910342447300_ref7) 1988; 66 Araujo (2020100910342447300_ref10) 2016; 129 Jamieson (2020100910342447300_ref3) 1873; 19 |
References_xml | – volume: 48 start-page: 199 year: 2007 ident: 2020100910342447300_ref5 article-title: A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita publication-title: J Dermatol Sci doi: 10.1016/j.jdermsci.2007.07.003 contributor: fullname: Liao – volume: 5 start-page: 58 year: 2018 ident: 2020100910342447300_ref2 article-title: An unusual case of facial steatocystoma multiplex: a clinicopathologic and dermoscopic report publication-title: Dermatopathology doi: 10.1159/000488584 contributor: fullname: Sharma – volume: 19 start-page: 223 year: 1873 ident: 2020100910342447300_ref3 article-title: Case of numerous cutaneous cysts scattered over the body publication-title: Edinb Med J contributor: fullname: Jamieson – volume: 29 start-page: 152 year: 2002 ident: 2020100910342447300_ref4 article-title: Clinical and histologic features of 64 cases of steatocystoma multiplex publication-title: J Dermatol doi: 10.1111/j.1346-8138.2002.tb00238.x contributor: fullname: Cho – volume: 66 start-page: 605 year: 1988 ident: 2020100910342447300_ref7 article-title: Steatocystoma simplex in the oral cavity: a previously undescribed condition publication-title: Oral Surg Oral Med Oral Pathol doi: 10.1016/0030-4220(88)90383-0 contributor: fullname: Olsen – volume: 129 start-page: 377 year: 2016 ident: 2020100910342447300_ref10 article-title: Clinical misdiagnosis of Steatocystoma simplex of eyebrow in a pediatric patient publication-title: Chin Med J doi: 10.4103/0366-6999.174493 contributor: fullname: Araujo – volume: 78 start-page: e1 year: 2017 ident: 2020100910342447300_ref8 article-title: Is routine pathologic evaluation of sebaceous cysts necessary?: a 15-year retrospective review of a single institution publication-title: Ann Plast Surg doi: 10.1097/SAP.0000000000000826 contributor: fullname: Gargya – volume: 64 start-page: 892 year: 2018 ident: 2020100910342447300_ref9 article-title: Numerous asymptomatic dermal cysts: diagnosis and treatment of steatocystoma multiplex publication-title: Can Fam Physician contributor: fullname: Georgakopoulos – volume: 139 start-page: 475 year: 1998 ident: 2020100910342447300_ref1 article-title: Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2 publication-title: Br J Dermatol doi: 10.1046/j.1365-2133.1998.02413.x contributor: fullname: Covello – volume: 7 start-page: 166 year: 2013 ident: 2020100910342447300_ref6 article-title: Steatocystoma multiplex-a rare genetic disorder: a case report and review of the literature publication-title: J Clin Diagn Res contributor: fullname: Kamra |
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Steatocystoma is a rare, benign cyst that mostly originates from a dermal sebaceous gland. It can be divided into steatocystoma multiplex—with... Steatocystoma is a rare, benign cyst that mostly originates from a dermal sebaceous gland. It can be divided into steatocystoma multiplex—with multiple... |
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Title | Palatal steatocystoma simplex—a rare oral finding at an even rarer location |
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