Suppr超能文献

太田痣病例的眼部特征

Ocular Features in a Case of Nevus of Ota.

作者信息

Junejo Murtaza Sameen, Khan Muhammad Saim, Mukhtar Ahsan

机构信息

Department of Ophthalmology, Armed Forces Institute of Ophthalmology, Mall Road, Military Hospital, Rawalpindi.

出版信息

J Coll Physicians Surg Pak. 2017 Mar;27(3):S56-S57.

Abstract

Oculodermal melanocytosis, also known as Nevus of Ota, is a hamartomatous melanocytic nevus of dermal melanocytes. It presents as a bluish grey patch on the face, which may be congenital or acquired involving the area of distribution of the ophthalmic and maxillary branches of the trigeminal nerve. The nevus can be unilateral or bilateral, and, in addition to skin, it may involve ocular and oral mucosal surfaces. It is a rare disorder and the ocular complications, such as glaucoma and melanoma, may be vision or life-threatening. Here, we report a 26-year male who presented with decreased vision in his left eye. On detailed examination, he turned out to be a case of nevus of Ota.

摘要

眼皮肤黑素细胞增多症,又称太田痣,是一种真皮黑素细胞错构瘤性黑素细胞痣。它表现为面部蓝灰色斑片,可为先天性或后天性,累及三叉神经眼支和上颌支分布区域。该痣可为单侧或双侧,除皮肤外,还可能累及眼和口腔黏膜表面。这是一种罕见疾病,眼部并发症如青光眼和黑色素瘤可能危及视力或生命。在此,我们报告一名26岁男性,其左眼视力下降。经详细检查,发现他是一例太田痣患者。

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