先天性颅神经支配障碍并发同侧眼眶绒毛膜瘤。

Arif O Khan
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引用次数: 0

摘要

一位患有右侧先天性颅神经支配障碍(外斜视,眼麻痹和上睑下垂)的20岁女性提出斜视手术。右眼检查证实眼外肌异常。外直肌收缩、内直肌扩张和下斜肌收缩改善了眼的初始位置。然而,术后出现一种不寻常的下位化脓,并持续了一个月。该组织的切除和组织学检查显示泪腺和软骨周围有炎症,提示眼眶绒毛膜瘤破裂。[J].中华眼科杂志,2010;33(6):559 - 561。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital Cranial Dysinnervation Disorder Complicated by Ipsilateral Orbital Choriostoma.

A 20-year-old woman with right-sided congenital cranial dysinnervation disorder (exotropia, ophthalmoplegia, and ptosis) presented for strabismus surgery. Exploration of the right eye confirmed abnormal extraocular muscles. Lateral rectus recession with medial rectus plication and inferior oblique recession improved primary position ocular alignment. However, an unusual pattern of inferior chemosis developed postoperatively and persisted during the next month. Excision and histologic examination of this tissue revealed areas of lacrimal gland and cartilage with surrounding inflammation, suggestive of a disrupted orbital choriostoma. [J Pediatr Ophthalmol Strabismus. 2022;59(6):e66-e68.].

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