新生儿原发性眼眶畸胎瘤合并先天性眼无:一例少见的组织病理学和放射学相关性。

IF 0.7 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmological Medicine Pub Date : 2025-06-27 eCollection Date: 2025-01-01 DOI:10.1155/crop/5032089
Dejan M Rašić, Dolika D Vasović, Miroslav Knežević
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引用次数: 0

摘要

本病例报告描述了一例罕见的原发性眼眶畸胎瘤合并无眼症的新生儿。一名6天大的女性,因先天性右眼眼眶肿胀及没有可见的眼部结构。MRI显示一个大的,血管充足的眼眶肿块,无颅内延伸,伴右脑半球畸形。组织病理学检查证实为良性、成熟/混合型畸胎瘤,包括神经外胚层、中胚层和内胚层,无恶性证据。患者在3周龄时接受了成功的眶内植入术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Orbital Teratoma With Congenital Anophthalmia in a Neonate: A Rare Case With Histopathological and Radiological Correlation.

This case report describes a rare instance of primary orbital teratoma with anophthalmia in a neonate. A 6-day-old female presented with a congenital right orbital swelling and absence of visible ocular structures. MRI revealed a large, well-vascularized orbital mass without intracranial extension, accompanied by malformations in the right cerebral hemisphere. Histopathological examination confirmed a benign, mature/mixed teratoma comprising elements from all three germ layers, including neuroectoderm, mesoderm, and endoderm, with no evidence of malignancy. The patient underwent successful orbital exenteration with an implant at 3 weeks of age.

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