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胎儿眼眶表皮样囊肿的产前产后影像学表现:病例报告及文献复习。

Fetal Orbital Epidermal Cyst Pre-postnatal Imaging Findings: A Case Report and Literature Review.

机构信息

Department of Radiology, Selcuk University, Faculty of Medicine, Konya, Turkey.

Department of Radiology, Gazi University, Faculty of Medicine, Ankara, Turkey.

出版信息

Curr Med Imaging. 2023;19(6):658-662. doi: 10.2174/1573405619666221129145104.

Abstract

BACKGROUND

Fetal ultrasonographic evaluation is a routine part of pregnancy follow-up, and examination of orbital structures is also part of the routine evaluation. Although orbital developmental anomalies are common in the neonatal period, diagnosis in the intrauterine period is not common. To our knowledge, three cases with a diagnosis of congenital orbital epidermal cysts have been reported in the literature, and two of them had fetal imaging findings. In this article, we present the prepostnatal imaging findings of a case diagnosed with orbital cyst in the fetal period and histopathologically diagnosed as epidermal cyst in the neonatal period.

CASE REPORT

A 25-year-old woman applied for ultrasonography (USG) examination at 22 weeks of gestation. A 35x45 mm cystic lesion causing proptosis, without solid component and vascularity, surrounding the optic nerve and causing its thinning was observed in the left orbit. In fetal magnetic resonance imaging (MRI), the intraorbital cystic lesion, which was hyperintense on T2W images and hypointense on T1W images, had no relationship with intracranial structures and no solid component. The lesion of the patient, followed up with a multidisciplinary approach, was shown similarly with computed tomography (CT) and magnetic resonance imaging (MRI) in the postnatal period. Subsequently, the patient underwent globe-sparing surgery, and the pathological diagnosis was made as the epidermal cyst.

CONCLUSION

Orbital epidermal cysts are rarely seen, and detection in the fetal period is even rarer. It should be considered in the differential diagnosis of orbital cystic lesions that cause proptosis in fetal and neonatal periods.

摘要

背景

胎儿超声检查是妊娠随访的常规内容,眼眶结构检查也是常规评估的一部分。尽管眼眶发育异常在新生儿期很常见,但在宫内期的诊断并不常见。据我们所知,文献中已有三例先天性眼眶表皮囊肿的诊断病例,其中两例有胎儿影像学发现。本文报道了一例在胎儿期诊断为眼眶囊肿,并在新生儿期经组织病理学诊断为表皮囊肿的病例的产前和产后影像学表现。

病例报告

一名 25 岁女性在妊娠 22 周时接受超声检查(USG)。在左眼发现一个 35x45 毫米的囊性病变,导致眼球突出,无实性成分和血管,视神经周围并使其变薄。在胎儿磁共振成像(MRI)中,眼眶内囊性病变在 T2W 图像上呈高信号,在 T1W 图像上呈低信号,与颅内结构无关系,也无实性成分。该病变通过多学科方法进行了随访,在产后的 CT 和 MRI 检查中表现相似。随后,患者接受了眼球保留手术,病理诊断为表皮囊肿。

结论

眼眶表皮囊肿罕见,在胎儿期检测更为罕见。在胎儿和新生儿期引起眼球突出的眼眶囊性病变的鉴别诊断中应考虑到该病变。

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