Gajec Sebastian, Składzień Jacek, Przeklasa Robert, Tomik Jerzy, Czopek Jacek
Klinika Otolaryngologii Collegium Medicum Uniwersytetu Jagiellońskiego w Krakowie.
Otolaryngol Pol. 2011 Jan-Feb;65(1):54-8. doi: 10.1016/S0030-6657(11)70628-X.
The aim of this study was to present a rare benign tumour of neural origin located in the orbit.
Authors describe case of six-year-old boy with tumour of the right orbit, upper eyelid and right zygomatic fossa. Medical history revealed gradually increasing in size, painless tumour. Before admission to the hospital computed tomography was taken to assess the size, localization of the tumour and to plan the proper treatment.
The patient was operated on using Krönlein approach. Tumour was removed in macroscopically radical limits without need to incise the muscles responsible for eye movement. Histopathological examination revealed: Neurothekeoma, classic type. During one year follow-up there was no recurrence.
Neurothekeoma may occur in young boys in eyelid and orbit. A unique localization of neurothekeoma in the orbit, close to the lacrimal gland shows that this kind of histopatological tumours may infiltrate deeper tissues. Surgical treatment of neurothekeoma is the same as in other benign tumours.
本研究旨在介绍一种罕见的起源于神经的位于眼眶的良性肿瘤。
作者描述了一名6岁男孩患有右侧眼眶、上眼睑及右侧颧窝肿瘤的病例。病史显示肿瘤大小逐渐增大,无痛。入院前进行了计算机断层扫描以评估肿瘤大小、位置并规划适当的治疗方案。
患者采用克伦莱因(Krönlein)入路进行手术。肿瘤在肉眼可见的根治范围内被切除,无需切开负责眼球运动的肌肉。组织病理学检查显示:经典型神经鞘黏液瘤。在一年的随访中未出现复发。
神经鞘黏液瘤可发生于年轻男性的眼睑和眼眶。神经鞘黏液瘤在眼眶中靠近泪腺的独特位置表明,这种组织病理学类型的肿瘤可能会浸润更深的组织。神经鞘黏液瘤的手术治疗与其他良性肿瘤相同。