Literature DB >> 15715135

The Laugier-Hunziker syndrome.

C Akcali1, G Serarslan, E Atik.   

Abstract

Laugier-Hunziker syndrome is a rare, acquired, benign hyperpigmentation of the lips, oral mucosa and nails. Although it is a benign disorder, other pigmentary disorders affecting the oral mucosa and nails must be considered in the different diagnosis. We presented a case of Laugier-Hunziker syndrome, showed clinical and histopathologic features of the disease.

Entities:  

Mesh:

Year:  2004        PMID: 15715135     DOI: 10.4314/eamj.v81i10.9240

Source DB:  PubMed          Journal:  East Afr Med J        ISSN: 0012-835X


  3 in total

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

Authors:  Verena Toedtling; Fiona Carol Crawford
Journal:  Clin Case Rep       Date:  2020-11-16

2.  Laugier-Hunziker syndrome.

Authors:  Ramakant S Nayak; Vijayalakshmi S Kotrashetti; Jagadish V Hosmani
Journal:  J Oral Maxillofac Pathol       Date:  2012-05

Review 3.  Mystery behind labial and oral melanotic macules: Clinical, dermoscopic and pathological aspects of Laugier-Hunziker syndrome.

Authors:  Ning Duan; Yang-Heng Zhang; Wen-Mei Wang; Xiang Wang
Journal:  World J Clin Cases       Date:  2018-09-26       Impact factor: 1.337

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.