Laugier-Hunziker Syndrome

Authors

  • Aldana Soledad Vacas Servicio de Dermatología. Hospital Italiano de Buenos Aires
  • Freddy Cabarcas Avila Servicio de Dermatología. Hospital Italiano de Buenos Aires
  • María Luz Bollea Garlatti Servicio de Dermatología. Hospital Italiano de Buenos Aires
  • Paula Enz Servicio de Dermatología. Hospital Italiano de Buenos Aires
  • Alicia M. Kowalczuk Servicio de Dermatología. Hospital Italiano de Buenos Aires

DOI:

https://doi.org/10.51987/Rev.Hosp.Ital.B.Aires.v36i3.667

Keywords:

Laugier-Hunziker syndrome, melanonychia, pigmentary disorder, lentiginosis

Abstract

Laugier-Hunziker syndrome is a rare acquired pigmentary disorder that is characterized by idiopathic mucocutaneous pigmentation that may be associated with longitudinal melanonychia. Although this syndrome is considered a benign disease with no systemic manifestations or malignant potential, it is important to rule out other mucocutaneous pigmentary disorders, especially Peutz-Jeghers syndrome. We report the case of a patient with this unusual syndrome

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References

Makhoul EN, Ayoub NM, Helou JF, et al. Familial Laugier-Hunziker syndrome. J Am Acad Dermatol. 2003;49(2 Suppl Case Reports):S143-5. DOI: https://doi.org/10.1067/mjd.2003.300

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Mignogna MD, Lo Muzio L, Ruoppo E, et al. Oral manifestations of idiopathic lenticular mucocutaneous pigmentation (Laugier-Hunziker syndrome): a clinical, histopathological and ultrastructural review of 12 cases. Oral Dis. 1999;5(1):80-6. DOI: https://doi.org/10.1111/j.1601-0825.1999.tb00068.x

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Published

2016-09-30

How to Cite

1.
Vacas AS, Cabarcas Avila F, Bollea Garlatti ML, Enz P, Kowalczuk AM. Laugier-Hunziker Syndrome. Rev Hosp Ital B.Aires [Internet]. 2016 Sep. 30 [cited 2026 Aug. 21];36(3):119-24. Available from: https://ojs.hospitalitaliano.org.ar/index.php/revistahi/article/view/667

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