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本文引用的文献

1
Epidermoid cyst in the floor of the mouth: report of a case.口底表皮样囊肿:一例报告
Quintessence Int. 2007 Jun;38(6):473-7.
2
Dermoid cysts (dermoids) of the floor of the mouth.口腔底部的皮样囊肿
Oral Surg Oral Med Oral Pathol. 1955 Nov;8(11):1149-64. doi: 10.1016/0030-4220(55)90380-7.
3
The place of fine-needle aspiration in the preoperative diagnosis of the congenital sublingual teratoid cyst.细针穿刺在先天性舌下畸胎样囊肿术前诊断中的作用
Diagn Cytopathol. 2003 Jul;29(1):33-7. doi: 10.1002/dc.10309.
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Carcinomatous transformation of a sublingual dermoid cyst. A case report.舌下皮样囊肿的癌性转化。病例报告。
Int J Oral Maxillofac Surg. 2000 Apr;29(2):126-7.
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Midline cystic lesion of the floor of the mouth.口腔底部中线囊性病变。
J Oral Maxillofac Surg. 1998 Jan;56(1):70-4. doi: 10.1016/s0278-2391(98)90919-3.
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Concomitant sublingual and submental epidermoid cysts: a case report.伴有舌下和颏下表皮样囊肿:一例报告。
J Oral Maxillofac Surg. 1993 Jul;51(7):790-2. doi: 10.1016/s0278-2391(10)80425-2.
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Dermoid cyst in the floor of the mouth. Review of the literature and case reports.口腔底部皮样囊肿。文献综述与病例报告
Oral Surg Oral Med Oral Pathol. 1994 Nov;78(5):567-76. doi: 10.1016/0030-4220(94)90166-x.
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Dermoid cysts of the floor of the mouth.
Br J Oral Surg. 1965 Jul;3(1):36-47. doi: 10.1016/s0007-117x(65)80005-1.
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口底表皮样囊肿伴颏下成分。

Epidermoid cyst in the floor of mouth with sub mental component.

作者信息

Tandon P N, Gupta D S

机构信息

Department of Oral and Maxillofacial Surgery, Teerthankar Mahaveer Dental College, House No. 1, Madhubani Duplex, Kanth Road, Moradabad, 244001 India.

出版信息

J Maxillofac Oral Surg. 2014 Mar;13(1):59-62. doi: 10.1007/s12663-010-0098-4. Epub 2011 Mar 25.

DOI:10.1007/s12663-010-0098-4
PMID:24644398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3955475/
Abstract

Epidermoid cysts in the oral cavity are very rare. They are slow and progressive in growth. Although congenital, they are diagnosed in second or third decayed of life. Epidermoid cyst in the floor of mouth is painless, doughy in consistency, fluctuant lesion and causes no symptoms until they are large enough to interfere with chewing or speech. In this article a 23 years old girl presented with lesion almost filling the oral cavity as well as sub mental component giving appearance of double chin. Lesion was surgically enucleated intraorally. Histopathological examination confirmed the presence of epidermoid cyst. Patient did well post operatively and there was no evidence of recurrence upto 1 year of follow up.

摘要

口腔表皮样囊肿非常罕见。它们生长缓慢且呈进行性。虽然是先天性的,但通常在生命的第二个或第三个十年被诊断出来。口底的表皮样囊肿无痛,质地如面团,有波动感,在囊肿足够大到影响咀嚼或说话之前不会引起任何症状。本文报道了一名23岁女性,其病变几乎占据整个口腔,并伴有颏下肿物,外观呈双下巴。病变通过口腔内手术摘除。组织病理学检查证实为表皮样囊肿。患者术后恢复良好,随访1年无复发迹象。