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口腔扁平苔藓硬化症:一例罕见病例报告及文献综述

Oral Lichen Sclerosus: A Rare Case Report and Review of the Literature.

作者信息

Marangon Júnior Helvécio, Souza Paulo Eduardo Alencar, Soares Rodrigo Villamarim, Gomez Ricardo Santiago, Pereira Gustavo Henrique de Mattos, Horta Martinho Campolina Rebello

机构信息

Oral Pathology Division, School of Dentistry, Pontifical Catholic University of Minas Gerais, Avenida Dom José Gaspar, 500, Prédio 46, Sala 101, Coração Eucarístico, Belo Horizonte, MG, 30535-901, Brazil.

Periodontology Division, School of Dentistry, Pontifical Catholic University of Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

Head Neck Pathol. 2017 Jun;11(2):212-218. doi: 10.1007/s12105-016-0766-x. Epub 2016 Nov 2.

Abstract

Lichen sclerosus (LS) is a chronic inflammatory mucocutaneous disease that often affects the anogenital area and causes significant discomfort and morbidity. Oral mucosal lesions in LS are extremely rare and might be associated with genital and/or skin manifestations. As a unique manifestation of LS, oral lesions are even more rare, with only 20 cases reported in English-language literature. In reviewing that literature in this paper, we present the case of a 44-year-old white man who sought dental assistance with a complaint of a white spot on his upper lip. Extraoral clinical examination revealed a slight white macule on the left upper lip vermilion next to the labial commissure. Intraoral examination revealed that the macule was approximately 3.5 × 2.0 cm, extended to the upper left labial mucosa, and presented an ivory-white color. Following an incisional biopsy and microscopy, the lesion was shown to be covered by a stratified squamous epithelium showing hyperkeratosis and atrophy. The superficial lamina propria revealed a well-marked band of subepithelial hyalinization and, below it, a band-like mononuclear inflammatory infiltrate. Sections stained by Verhoeff's technique revealed a scantiness of elastic fibers in the superficial lamina propria. The diagnosis of LS was then established. The patient was referred for dermatologic evaluation, which identified no skin or genital lesions, and no treatment was employed. After 6 years, no significant changes in clinical features were observed. Altogether, this rare case makes an important contribution to knowledge on this uncommon condition.

摘要

硬化性苔藓(LS)是一种慢性炎症性黏膜皮肤疾病,常累及肛门生殖器区域,可引起明显不适和发病。LS的口腔黏膜病变极为罕见,可能与生殖器和/或皮肤表现相关。作为LS的一种独特表现,口腔病变更为罕见,英文文献中仅报道过20例。在本文回顾该文献时,我们报告了一例44岁白人男性的病例,他因上唇出现白斑而寻求牙科帮助。口腔外临床检查发现,在唇联合旁的左上唇唇红处有一个轻微的白色斑疹。口腔内检查发现,该斑疹大小约为3.5×2.0cm,延伸至左上唇黏膜,呈象牙白色。经切开活检及显微镜检查,病变表面覆盖有分层鳞状上皮,表现为角化过度和萎缩。固有层浅层显示明显的上皮下玻璃样变带,其下方为带状单核炎性浸润。用韦尔霍夫氏技术染色的切片显示固有层浅层弹性纤维稀少。随后确诊为LS。该患者被转诊进行皮肤科评估,未发现皮肤或生殖器病变,未采取任何治疗措施。6年后,临床特征未观察到明显变化。总之,这个罕见病例为了解这种罕见疾病提供了重要资料。

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