Suppr超能文献

劳吉尔-洪齐克综合征:一例儿科患者病例报告及文献复习。

Laugier-Hunziker syndrome: a case report of the pediatric patient and review of the literature.

机构信息

Division of Anatomy, Department of Human Morphology and Embryology, Wroclaw Medical University, Poland.

Department of Pathomorphology, Wroclaw Medical University, Poland.

出版信息

Int J Dermatol. 2020 Dec;59(12):1513-1519. doi: 10.1111/ijd.15262. Epub 2020 Oct 29.

Abstract

Laugier-Hunziker syndrome (LHS) is a rare, idiopathic pigmentary disorder especially affecting the lips and oral mucosa. At present, no more than 200 cases of patients diagnosed with LHS syndrome have been described worldwide. To date, three patients under the age of 20 have been described, including the youngest patient who is a 12-year-old child. The exact etiology of LHS still remains uncertain, as there is no evidence of systemic symptoms or increased cancer risk. The final diagnosis of LHS is possible after the exclusion of other, more serious diseases involving skin-mucosal hyperpigmentation, mainly Peutz-Jeghers syndrome (PJS) and Addison's disease (AD). Herein, we present a 16-year-old patient who has been diagnosed with oral hyperpigmentation since the age of 13. We reviewed the clinical and histological findings. In addition, we discussed the differential diagnosis of mucocutaneous hyperpigmentation.

摘要

劳吉尔-洪齐克综合征(LHS)是一种罕见的特发性色素沉着疾病,特别影响嘴唇和口腔黏膜。目前,全世界描述的 LHS 综合征患者病例不超过 200 例。迄今为止,已经描述了 3 名年龄在 20 岁以下的患者,其中最年轻的患者为 12 岁儿童。由于没有系统性症状或癌症风险增加的证据,LHS 的确切病因仍不确定。排除其他更严重的皮肤黏膜色素沉着疾病(主要为皮杰氏综合征和爱迪生病)后,才能最终诊断为 LHS。在此,我们介绍了一名 16 岁的患者,他从 13 岁开始就被诊断为口腔色素沉着。我们回顾了他的临床和组织学检查结果。此外,我们还讨论了黏膜皮肤色素沉着的鉴别诊断。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验