劳吉尔-杭齐克尔综合征的临床及组织病理学鉴别诊断：一例极为罕见的伴有异常广泛口腔色素沉着的病例

Clinical and histopathological differential diagnosis of Laugier-Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation.

作者信息

Toedtling Verena, Crawford Fiona Carol

机构信息

Division of Dentistry School of Medical Sciences Faculty of Biology, Medicine and Health, Oral and Maxillofacial Surgery The University of Manchester Manchester UK.

Retired Oral Medicine Consultant Edinburgh UK.

出版信息

Clin Case Rep. 2020 Nov 16;9(1):309-313. doi: 10.1002/ccr3.3522. eCollection 2021 Jan.

DOI:10.1002/ccr3.3522

PMID:33489178

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7813034/

Abstract

Laugier-Hunziker syndrome is a rare and benign disorder characterized by hyperpigmentation of the lips and buccal mucosae with associated longitudinal melanonychia of nails. Clinical correlation is needed to rule out other pigmentary disorders.

摘要

劳吉尔-杭齐克尔综合征是一种罕见的良性疾病，其特征为唇部和颊黏膜色素沉着伴指甲纵向黑甲。需要进行临床关联以排除其他色素沉着障碍。