Posible asociación autoinmune entre síndrome de Laugier-Hunziker y síndrome de Sjögren: reporte de un caso y revisión de la literatura / Laugier-Hunziker syndrome in a patient with Sjögrens syndrome: report of one case
Rev. méd. Chile
; 144(5): 671-674, mayo 2016. ilus, tab
Article
in Es
| LILACS
| ID: lil-791056
Responsible library:
CL1.1
ABSTRACT
Laugier-Hunziker syndrome is a rare benign idiopathic condition characterized by acquired macular pigmentation of lips and buccal mucosa, often accompanied with melanonychia. The main concern with this condition is to rule out other differential diagnosis with systemic repercussions and similar hyperpigmentation patterns, such as Peutz-Jeghers syndrome, adrenal insufficiency and melanoma. We report a 58-year-old female with a 20-year history of Sjögrens syndrome, presenting with melanonychia and hyperpigmentation in the buccal mucosa. She had no relevant medication history and is a non-smoker. The patient denied any other symptoms. The histopathology confirmed the diagnosis of Laugier-Hunziker syndrome.
Key words
Full text:
1
Collection:
01-internacional
Database:
LILACS
Main subject:
Sjogren's Syndrome
/
Hyperpigmentation
/
Mouth Diseases
/
Nail Diseases
Limits:
Female
/
Humans
Language:
Es
Journal:
Rev. méd. Chile
Journal subject:
MEDICINA
Year:
2016
Document type:
Article
Affiliation country:
Chile
Country of publication:
Chile