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可疑光化性唇炎的恰当管理。

Proper management of suspicious actinic cheilitis.

作者信息

Kim Soung Min, Myoung Hoon, Eo Mi Young, Cho Yun Ju, Lee Suk Keun

机构信息

Oral and Maxillofacial Microvascular Reconstruction LAB, Brong Ahafo Regional Hospital, Sunyani, Ghana.

2Department of Oral and Maxillofacial Surgery, Dental Research Institute, School of Dentistry, Seoul National University, 101 Daehak-ro, Jongno-gu, Seoul, 110-768 South Korea.

出版信息

Maxillofac Plast Reconstr Surg. 2019 Apr 9;41(1):15. doi: 10.1186/s40902-019-0198-0. eCollection 2019 Dec.

Abstract

BACKGROUND

Actinic cheilitis (AC) is a variant of actinic keratosis which is known to be a premalignant condition that could develop into squamous cell carcinoma (SCC). Epimyoepithelial carcinoma (EC) is a very rare salivary gland (SG) neoplasm that has classical biphasic histologic findings of small tubules and glandular lumina surrounded by clear myoepithelial cells.

CASE PRESENTATION

We report a very rare case of AC occurring on the lower lip of a 70-year-old woman, which is developing to the EC later.

CONCLUSIONS

Diverse appearances of AC include edematous reddish in the acute stage and grey-whitish or dried hyperkeratotic wrinkled lesions in the chronic stage for several months or even years. Accurate treatment of AC in its initial stage could be recommended to avoid further malignant transformation; proper management of clinically suspicious AC is suggested.

摘要

背景

光化性唇炎(AC)是光化性角化病的一种变体,已知是一种可能发展为鳞状细胞癌(SCC)的癌前病变。肌上皮癌(EC)是一种非常罕见的涎腺(SG)肿瘤,具有典型的双相组织学表现,即由透明肌上皮细胞围绕的小管和腺腔。

病例报告

我们报告了一例非常罕见的发生在一名70岁女性下唇的AC病例,该病例后来发展为EC。

结论

AC的表现多样,急性期为水肿性发红,慢性期数月甚至数年为灰白色或干燥的角化过度皱纹病变。建议在AC的初始阶段进行准确治疗以避免进一步恶变;建议对临床上可疑的AC进行适当管理。

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