Síndrome Laugier-Hunziker, en el adulto mayor

Q4 Medicine
Juan Sebastian Theran León , Laura Yibeth Esteban Badillo , Luis Andres Dulcey
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引用次数: 0

Abstract

Laugier-Hunziker syndrome (LHS) is a rare benign disorder, often acquired in adulthood, characterized by lentiginous hyperpigmentation of the oral mucosa and lips, associated with longitudinal melanonychia. Its importance is based on the early recognition and differential diagnosis of various oral and cutaneous hyperpigmentation pathologies. The case of a 74-year-old man with probable SLH is presented below and important differential diagnoses are discussed.

Laugier-Hunziker综合征,老年人
Laugier-Hunziker综合征(LHS)是一种罕见的良性疾病,通常在成年期获得,其特征是口腔黏膜和嘴唇的黄斑性色素沉着,并伴有纵向黑甲癣。它的重要性在于对各种口腔和皮肤色素沉着病的早期识别和鉴别诊断。以下是一例74岁男性SLH的病例,并讨论了重要的鉴别诊断。
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来源期刊
Atencion Primaria Practica
Atencion Primaria Practica Medicine-Family Practice
CiteScore
0.30
自引率
0.00%
发文量
40
审稿时长
24 days
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