Literature DB >> 3819089

Laugier-Hunziker syndrome.

S E Koch, P E LeBoit, R B Odom.   

Abstract

The Laugier-Hunziker syndrome represents a rare acquired pigmentary disorder of the lips, oral mucosa, and nails. We report the first case of this syndrome to be recognized in the United States and review other causes of hyperpigmentation in these locations.

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Mesh：

Year:  1987        PMID： 3819089     DOI： 10.1016/s0190-9622(87)70055-3

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN： 0190-9622            Impact factor:   11.527


  5 in total

1.  Laugier-hunziker syndrome: an uncommon cause of oral pigmentation and a review of the literature.

Authors:  Lucio Montebugnoli; Ivana Grelli; Fabio Cervellati; Cosimo Misciali; Beatrice Raone
Journal:  Int J Dent       Date:  2010-07-07

2.  Laugier-hunziker syndrome: a rare cause of oral and acral pigmentation.

Authors:  Silonie Sachdeva; Shabina Sachdeva; Pranav Kapoor
Journal:  J Cutan Aesthet Surg       Date:  2011-01

3.  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

4.  Laugier-Hunziker syndrome: a case of asymptomatic mucosal and acral hyperpigmentation.

Authors:  Elizabeth H Cusick; Ashfaq A Marghoob; Ralph P Braun
Journal:  Dermatol Pract Concept       Date:  2017-04-30

Review 5.  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
  5 in total

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