Laugier-hunziker syndrome

Authors

  • Rodrigo Guerra Sabongi Escola Paulista de Medicina - Universidade Federal de São Paulo (EPM-UNIFESP)
  • Natalia Petri Dias Escola Paulista de Medicina - Universidade Federal de São Paulo (EPM-UNIFESP)
  • Julia Rezende Duek FCMS/PUC-SP
  • Vânia Penha Guerra Sabongi

Keywords:

hyperpigmentation, syndrome, dermocospy, lentigo.

Abstract

ABSTRACT Laugier-Hunziker syndrome is a rare benign acquired disorder of unknown pathogenesis, firstly described in 1970, characterized by macular mucocutaneous hyperpigmentation frequently associated with longitudinal melanonychia. Diagnosis is essentially clinical, therefore other causes of mucocutaneous hyperpigmentation in which dermatoscopy can correlate with histological findings of the syndrome must be excluded. We report a case of Laugier-Hunziker syndrome based on clinical and dermatoscopic findings.

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Author Biographies

Rodrigo Guerra Sabongi, Escola Paulista de Medicina - Universidade Federal de São Paulo (EPM-UNIFESP)

Acadêmico do curso de Medicina UNIFESP

Natalia Petri Dias, Escola Paulista de Medicina - Universidade Federal de São Paulo (EPM-UNIFESP)

Acadêmica do curso de Medicina UNIFESP

Julia Rezende Duek, FCMS/PUC-SP

Acadêmica do curso de Medicina FCMS/PUC-SP

Vânia Penha Guerra Sabongi

Médica dermatologista. Membro Titular da Sociedade Brasileira de Dermatologia (SBD)

References

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Published

2012-06-27

How to Cite

1.
Sabongi RG, Dias NP, Duek JR, Sabongi VPG. Laugier-hunziker syndrome. Rev. Fac. Ciênc. Méd. Sorocaba [Internet]. 2012Jun.27 [cited 2024Jun.29];14(2):67-70. Available from: https://revistas.pucsp.br/index.php/RFCMS/article/view/6274

Issue

Section

Case Report

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