Dermoscopic features of conjunctival, mucosal, and nail pigmentations in a case of Laugier-Hunziker syndrome
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منابع مشابه
Dermoscopic features of conjunctival, mucosal, and nail pigmentations in a case of Laugier-Hunziker syndrome
A 23-year-old man presented with multiple lip pigmentations. Longitudinal hyperpigmented streaks on his nails, as well as an ill-defined 2x3 mm pigmented spot on his right eye were noted (Figure 1). The family history was unremarkable. He was not taking any medication. Colonoscopy and barium radiography of intestine were unremarkable. Complete blood count, complete metabolic panel, and urinalys...
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متن کاملDermoscopic findings in Laugier-Hunziker syndrome.
BACKGROUND Laugier-Hunziker syndrome (LHS) is a rare, acquired mucocutaneous hyperpigmentation often associated with longitudinal melanonychia. The clinical behavior of mucocutaneous pigmented lesions ranges from benign to highly malignant. Therefore, in most cases, the clinical diagnosis should be confirmed by further diagnostic methods. Dermoscopy is a noninvasive technique that has been used...
متن کاملLaugier-Hunziker syndrome - Case report*
Laugier-Hunziker syndrome is a rare, acquired disorder characterized by lenticular hyperpigmentation of the oral mucosa and longitudinal melanonychia. We present the case of a 63-year-old female with progressive, asymptomatic hyperpigmentation of buccal mucosa and a 7-year history of hyperpigmentation in several fingernails. Laugier-Hunziker syndrome was diagnosed based on the clinical features...
متن کاملA Case of Laugier-Hunziker Syndrome.
Laugier-Hunziker syndrome is a rare idiopathic acquired hyperpigmentation of oral mucosa and lips which is often associated with longitudinal melanonychia. This condition is known to be an entirely benign disease with no systemic manifestations. Herein we report a case of a 54-year-old woman presenting with a 7-year history of asymptomatic oral pigmentation and linear pigmented streaks of sever...
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ژورنال
عنوان ژورنال: Dermatology Practical & Conceptual
سال: 2016
ISSN: 2160-9381
DOI: 10.5826/dpc.0601a07