Gabbard Ryan, Harrison Hunter, Chang Kenneth, Pogrebniak Elizabeth, Keck Katie, Patel Rakesh M
University of South Carolina/Prisma Health, Columbia, SC, USA.
University of Toronto, Toronto, Ontario, Canada.
Am J Ophthalmol Case Rep. 2024 Dec 12;37:102230. doi: 10.1016/j.ajoc.2024.102230. eCollection 2025 Mar.
The purpose of this manuscript is to report a rare case of an orbital cyst detected intrauterine with sonography.
A 23-year-old female presented for routine prenatal monitoring when an orbital cyst was detected with a transabdominal ultrasound. Uncomplicated cesarean section was performed at 38 weeks gestation with proptosis of the left globe being noted on ophthalmic examination of the newborn. Magnetic resonance imaging was conducted which demonstrated a cystic mass suspicious for lymphatic malformation. Surgical intervention was performed shortly after birth with pathological results demonstrating non-keratinizing squamous epithelium consistent with conjunctivoid variant of dermoid cyst. Post-operative examination demonstrated significant improvement of the exophthalmos with minimal lagophthalmos.
Congenital orbital cysts are a rare phenomenon with only a handful of cases being detected during the fetal period. We recommend physicians include this rare variant of dermoid cysts in their differential diagnosis for orbital lesions that can cause proptosis in the fetal period.
本手稿旨在报告一例罕见的经超声在子宫内检测出的眼眶囊肿病例。
一名23岁女性在进行常规产前监测时,经腹部超声检测出眼眶囊肿。妊娠38周时进行了无并发症的剖宫产,新生儿眼科检查发现左眼眼球突出。进行了磁共振成像,显示有一个疑似淋巴管畸形的囊性肿块。出生后不久进行了手术干预,病理结果显示为非角化鳞状上皮,与皮样囊肿的结膜样变体一致。术后检查显示眼球突出明显改善,仅有轻微睑裂闭合不全。
先天性眼眶囊肿是一种罕见现象,在胎儿期仅检测到少数病例。我们建议医生在对可导致胎儿期眼球突出的眼眶病变进行鉴别诊断时,将这种罕见的皮样囊肿变体考虑在内。