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孤立性口腔角化棘皮瘤

Solitary intraoral keratoacanthoma.

作者信息

Svirsky J A, Freedman P D, Lumerman H

出版信息

Oral Surg Oral Med Oral Pathol. 1977 Jan;43(1):116-22. doi: 10.1016/0030-4220(77)90360-7.

Abstract

A case of keratoacanthoma of the maxillary gingiva in a 12-year-old white boy has been presented. This is only the fourth case of solitary intraoral keratoacanthoma reported in the English-language literature. A review of the literature on solitary and multiple mucosal keratoacanthomas and the incidence of ectopic sebaceous glands has been included. In all mucous membrane locations where keratoacanthomas have arisen, there have been other reported cases of ectopic sebaceous glands in these areas. These findings have led us to consider that intraoral and perhaps all mucous membrane keratoacanthomas arise i, sebaceous glands or their ducts, whether they be normal in their location, as in the buccal mucosa, or ectopic.

摘要

本文报告了一名12岁白人男孩上颌牙龈发生角化棘皮瘤的病例。这是英文文献中报道的第四例孤立性口腔内角化棘皮瘤。文中还综述了关于孤立性和多发性黏膜角化棘皮瘤以及异位皮脂腺发生率的文献。在所有出现角化棘皮瘤的黏膜部位,均有其他关于这些区域异位皮脂腺的报道病例。这些发现使我们认为,口腔内乃至所有黏膜角化棘皮瘤均起源于皮脂腺或其导管,无论其位置是正常的,如颊黏膜,还是异位的。

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