[Laugier-Hunziker syndrome : A rare differential diagnosis of mucocutaneous hyperpigmentation].

4区医学 Q3 Medicine

Hautarzt Pub Date : 2022-04-01 Epub Date: 2021-06-25 DOI:10.1007/s00105-021-04845-x

Sören Korsing, Marcel Boede, Schokufe Ebrahimsade, Katharina Meier

引用次数: 2

Abstract

Laugier-Hunziker syndrome (LHS) is characterized by lentiginous hyperpigmentation of the oral mucosa and lips. In addition, longitudinal melanonychia and palmoplantar hyperpigmented lesions may occur. LHS is a clinical diagnosis of exclusion. Herein, we report the case of a 66-year-old woman with LHS. The clinical and histopathologic features of LHS are presented and important differential diagnoses are discussed.

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[Laugier-Hunziker综合征:一种罕见的粘膜色素沉着的鉴别诊断]。

Laugier-Hunziker综合征(LHS)的特征是口腔黏膜和嘴唇的黄斑性色素沉着。此外，纵向黑色素瘤和掌足底色素沉着病变也可能发生。LHS是一种排除性临床诊断。在此，我们报告一例66岁女性LHS。本文介绍了LHS的临床和组织病理学特征，并讨论了重要的鉴别诊断。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Hautarzt 医学-皮肤病学

CiteScore

1.40

自引率

0.00%

发文量

审稿时长

4-8 weeks

期刊介绍： Der Hautarzt is an internationally recognized journal informing all dermatologists working in practical or clinical environments about important developments in the field of dermatology including allergology, venereology and related areas. Comprehensive reviews on a specific topical issue focus on providing evidenced based information on diagnostics and therapy. Freely submitted original papers allow the presentation of important clinical studies and serve the scientific exchange. Case reports feature interesting cases and aim at optimizing diagnostic and therapeutic strategies. Review articles under the rubric "Continuing Medical Education" present verified results of scientific research and their integration into daily practice.