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LAUGIER-HUNZIKER SYNDROME IN A PATIENT WITH SJÖGREN’S SYNDROME. REPORT OF ONE CASE

dc.contributorClínica Alemana de Santiago, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo, Hospital Padre Hurtado. Santiago, Chile.es-ES
dc.contributoren-US
dc.creatorFajre, Ximena; Departamento de dermatología, Clínica Alemana de Santiago, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo, Hospital Padre Hurtado. Santiago, Chile.
dc.creatorAspillaga, María; Departamento de dermatología, Clínica Alemana de Santiago, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo. Santiago, Chile.
dc.creatorMcNab, María; Práctica privada
dc.creatorNavarrete, Jorge; Práctica privada
dc.creatorSanhueza, Verónica; Departamento de anatomía patológica, Hospital Padre Hurtado. Santiago, Chile.
dc.creatorBenedetto, Juana; Departamento de dermatología, Clínica Alemana de Santiago, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo, Hospital Padre Hurtado. Santiago, Chile.
dc.date2016-05-12
dc.date.accessioned2019-11-11T18:26:18Z
dc.date.available2019-11-11T18:26:18Z
dc.identifierhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/view/4474
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/110616
dc.descriptionLaugier-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 Sjögren’s 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.es-ES
dc.descriptionLaugier-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 years old female with a 20 years history of Sjögren’s syndrome, presenting with melanonychia and hyperpigmentation in the buccal mucosa. She had no relevant medication history and is a non-smoker. She patient denied any other symptoms. The histopathology confirmed the diagnosis of Laugier-Hunziker syndrome.en-US
dc.formatapplication/pdf
dc.languagespa
dc.publisherRevista Médica de Chilees-ES
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dc.sourceRevista Médica de Chile; Vol. 144, núm. 5 (2016): MAYO 2016es-ES
dc.source0034-9887
dc.subjectAutoimmunity; Hyperpigmentation; Mouth Mucosa; Pigmentation Disorders; Sjogren´s Syndromees-ES
dc.subjectAutoimmunity; Hyper pigmentation; Mouth Mucosa; Pigmentation Disorders; Sjogren´s Syndromeen-US
dc.titlePosible asociación autoinmune entre síndrome de Laugier-Hunziker y síndrome de Sjögren: reporte de un caso y revisión de la literatura.es-ES
dc.titleLAUGIER-HUNZIKER SYNDROME IN A PATIENT WITH SJÖGREN’S SYNDROME. REPORT OF ONE CASEen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typees-ES


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