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Palatal steatocystoma simplex-a rare oral finding at an even rarer location.

作者信息

Kaya Sebahat, Zimmer Stefanie, Kämmerer Peer Wolfgang

机构信息

Department of Oral, Maxillofacial and Plastic Surgery, University Medical Center Mainz, Mainz, Germany.

Department of Pathology, University Medical Center Mainz, Mainz, Germany.

出版信息

J Surg Case Rep. 2020 Oct 9;2020(10):rjaa347. doi: 10.1093/jscr/rjaa347. eCollection 2020 Oct.

DOI:10.1093/jscr/rjaa347
PMID:33072253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7546247/
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.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/59731fce7197/rjaa347f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/62e286970810/rjaa347f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/50c46856bae3/rjaa347f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/8a297016ac0c/rjaa347f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/1c259d0f4bd9/rjaa347f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/1162261335d8/rjaa347f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/59731fce7197/rjaa347f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/62e286970810/rjaa347f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/50c46856bae3/rjaa347f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/8a297016ac0c/rjaa347f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/1c259d0f4bd9/rjaa347f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/1162261335d8/rjaa347f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/7546247/59731fce7197/rjaa347f6.jpg

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引用本文的文献

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本文引用的文献

1
Numerous asymptomatic dermal cysts: Diagnosis and treatment of steatocystoma multiplex.多发性无症状皮肤囊肿：多发性脂囊瘤的诊断和治疗。
Can Fam Physician. 2018 Dec;64(12):892-899.
2
An Unusual Case of Facial Steatocystoma Multiplex: A Clinicopathologic and Dermoscopic Report.多发性面部皮脂腺囊肿1例罕见病例：临床病理及皮肤镜报告
Dermatopathology (Basel). 2018 May 22;5(2):58-63. doi: 10.1159/000488584. eCollection 2018 Apr-Jun.
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Case of Numerous Cutaneous Cysts Scattered over the Body.全身散在多发性皮肤囊肿病例
Edinb Med J. 1873 Sep;19(3):223-225.
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Is Routine Pathologic Evaluation of Sebaceous Cysts Necessary?: A 15-Year Retrospective Review of a Single Institution.
Ann Plast Surg. 2017 Feb;78(2):e1-e3. doi: 10.1097/SAP.0000000000000826.
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Clinical Misdiagnosis of Steatocystoma Simplex of Eyebrow in a Pediatric Patient.一名儿科患者眉部单纯性脂囊瘤的临床误诊
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Steatocystoma multiplex-a rare genetic disorder: a case report and review of the literature.多发性皮脂囊肿——一种罕见的遗传性疾病：病例报告及文献综述
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A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita.角蛋白K6a、K16和K17中的一系列突变导致先天性厚甲症。
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Clinical and histologic features of 64 cases of steatocystoma multiplex.
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Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2.角蛋白17突变会导致多发性皮脂囊肿或2型先天性厚甲症。
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Steatocystoma simplex in the oral cavity: a previously undescribed condition.
Oral Surg Oral Med Oral Pathol. 1988 Nov;66(5):605-7. doi: 10.1016/0030-4220(88)90383-0.