Affiliation:
1. Department of Radiology, Selcuk University, Faculty of Medicine, Konya, Turkey
2. Department of Radiology, Gazi
University, Faculty of Medicine, Ankara, Turkey
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.
Publisher
Bentham Science Publishers Ltd.
Subject
Radiology, Nuclear Medicine and imaging