Suppr超能文献

皮肤朗格汉斯细胞组织细胞增多症中的多发性眼睑缺损

Multiple eyelid defects in cutaneous Langerhans cell histiocytosis.

作者信息

Wat Christina S K, Yuen Hunter K L, Tse K K, Lam Dennis S C, Chan Nongnart

机构信息

Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong Eye Hospital, Kowloon, Hong Kong SAR, People's Republic of China.

出版信息

Ophthalmic Plast Reconstr Surg. 2006 May-Jun;22(3):216-8. doi: 10.1097/01.iop.0000217567.90717.52.

Abstract

Langerhans cell histiocytosis is a disorder characterized by the proliferation of histiocytes of the mononuclear phagocyte system. Cutaneous Langerhans cell histiocytosis can develop as a solitary lesion or more frequently as part of a multisystem disease. This report describes a case of cutaneous Langerhans cell histiocytosis affecting the eyelids, resulting in a coloboma-like defect. The clinical features and management are discussed.

摘要

朗格汉斯细胞组织细胞增多症是一种以单核吞噬细胞系统组织细胞增殖为特征的疾病。皮肤朗格汉斯细胞组织细胞增多症可表现为孤立性病变,或更常见地作为多系统疾病的一部分出现。本报告描述了一例累及眼睑的皮肤朗格汉斯细胞组织细胞增多症病例,导致类似睑裂缺损的缺陷。并对其临床特征及治疗进行了讨论。

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