de Sales Sarah Campos, Oliveira Sicília Rezende, Pantuzzo Erika Soares, Costa Fernanda Pereira Delgado, Xavier Marcus Henrique, de Mesquita Ricardo Alves, Abreu Lucas Guimarães, Campos Felipe Eduardo Baires, de Castro Wagner Henriques, Silva Tarcília Aparecida
Oral and Maxillofacial Surgery Residency, Hospital das Clínicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Department of Oral Surgery and Pathology, Faculdade de Odontologia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Int J Dermatol. 2023 Feb;62(2):154-168. doi: 10.1111/ijd.16165. Epub 2022 Mar 22.
Cheilitis glandularis (CG) is a rare inflammatory disease of unknown etiology that affects the minor salivary glands predominantly in the lower lip. In this article, we report the case of an 18-year-old black woman who presented with a deep suppurative type of CG in both lips. In addition, we performed a systematic literature review in five databases (PubMed, Scopus, Web of Science, Ovid, and Embase) to identify CG case reports or case series. A total of 360 references were retrieved in the electronic databases. Thirty-four articles met the inclusion criteria, and six were retrieved through manual search, totaling 40 articles included in the systematic review. Thirty-nine (68.4%) cases occurred in male individuals and 18 (31.6%) in female individuals. The mean age of affected individuals was 40.9 years. Different clinical manifestations ranging from no symptoms to discomfort, pain, swelling, erythema, eversion of the lip, dilated ductal openings, ulcers, and crust have been reported. Among the included CG cases, 41 affected exclusively the lower lip (71.9%). In four cases, the CG only affected the upper lip (7.0%). In 12 cases, the lesion affected both the lower and upper lips (21.1%). Different treatment modalities were adopted in the management of CG. Although the surgical treatment was indicated (42.1%), the conservative treatment with topical medications, as in the present case, resulted in resolution in 21.0% of cases.
腺性唇炎(CG)是一种病因不明的罕见炎症性疾病,主要累及下唇的小唾液腺。在本文中,我们报告了一名18岁黑人女性的病例,她双唇均出现深部化脓型腺性唇炎。此外,我们在五个数据库(PubMed、Scopus、Web of Science、Ovid和Embase)中进行了系统的文献综述,以确定腺性唇炎的病例报告或病例系列。电子数据库共检索到360篇参考文献。34篇文章符合纳入标准,通过手工检索又获得6篇,系统综述共纳入40篇文章。39例(68.4%)发生在男性个体,18例(31.6%)发生在女性个体。受影响个体的平均年龄为40.9岁。已报告了从无症状到不适、疼痛、肿胀、红斑、唇外翻、导管开口扩张、溃疡和结痂等不同的临床表现。在纳入的腺性唇炎病例中,41例仅累及下唇(71.9%)。4例中,腺性唇炎仅累及上唇(7.0%)。12例中,病变累及上下唇(21.1%)。腺性唇炎的治疗采用了不同的治疗方式。尽管手术治疗是首选(42.1%),但如本病例中采用局部药物的保守治疗,在21.0%的病例中取得了治愈效果。