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孤立性巩膜上神经纤维瘤。

Isolated episcleral neurofibroma.

作者信息

Perry H D

出版信息

Ophthalmology. 1982 Sep;89(9):1095-8. doi: 10.1016/s0161-6420(82)34678-3.

Abstract

A 22-year-old white woman presented with an epibulbar tumor of the right eye first noted seven years previously. Clinical examination showed a 6 x 8 mm lobulated yellowish white tumor rising 3-4 mm off the inferior bulbar surface. An excisional biopsy revealed the tumor to be free of conjunctival attachments and be firmly fixed to the sclera. Smaller nodules were noted away from the main tumor and posterior to the equator. The histopathologic evaluation revealed the tumor to be an isolated episcleral neurofibroma. Although rare, isolated episcleral neurofibromas should be thought of in the differential diagnosis of epibulbar tumors and treated conservatively.

摘要

一名22岁的白人女性因右眼球结膜下肿瘤就诊,该肿瘤七年前首次被发现。临床检查显示,一个6×8毫米的分叶状黄白色肿瘤从眼球下表面隆起3 - 4毫米。切除活检显示,肿瘤与结膜无粘连,与巩膜紧密相连。在远离主肿瘤和赤道后方发现了较小的结节。组织病理学评估显示,该肿瘤为孤立性巩膜神经纤维瘤。尽管孤立性巩膜神经纤维瘤罕见,但在眼球表面肿瘤的鉴别诊断中应予以考虑,并采用保守治疗。

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