先天性眼球囊1例的治疗:附文献复习

IF 0.7 Q4 OPHTHALMOLOGY Case Reports in Ophthalmological Medicine Pub Date : 2022-05-23 DOI:10.1155/2022/3945537
Aashish Raj Pant, Rinkal Suwal, Purushottam Joshi, Santosh Chaudhary
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引用次数: 0

摘要

先天性囊性眼球是一种极其罕见的疾病,迄今为止文献中仅报道了52例。在妊娠第四周,由于初级视神经囊完全或部分内陷失败,眼眶囊肿取代眼球。我们讨论一个先天性囊肿性眼球的情况下,14岁的女性谁提出了一个美容缺陷,由于一个大的肿胀在右眼睑与右眼球的缺失,因为出生。她接受了囊肿切除,随后进行了眼眶植入和后来的假体。根据临床和b超特征,术中发现和组织病理学报告,对先天性囊性眼球做出诊断。本文在已有文献的基础上增加了一例先天性囊性眼球。在我们的病例中,囊肿切除后眶内植入假体提供了明确的诊断和良好的美容结果。
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Managing a Case of a Congenital Cystic Eyeball: Case Report with Review of Literature
A congenital cystic eyeball is an extremely rare condition, with only 52 cases reported in the literature to date. An orbital cyst replaces the eyeball which occurs due to the complete or partial failure in invagination of the primary optic vesicle during the fourth week of gestation. We discuss a case of a congenital cystic eyeball in a 14-year-old female who presented to us for a cosmetic blemish due to a large swelling in the right eyelid with the absence of a right eyeball since birth. She underwent removal of the cyst followed by an orbital implant and later prosthesis. Diagnosis of the congenital cystic eyeball was made based on the clinical and ultrasound B-scan features, intraoperative findings, and histopathology report. This article adds one more case to the existing literature on the congenital cystic eyeball. Orbital implant with prosthesis after excision of the cyst provided definitive diagnosis and a good cosmetic outcome in our case.
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审稿时长
14 weeks
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