Vara Thorbeck R, Morales Valentin O I, Ruiz Morales M
Zentralbl Chir. 1986;111(1):46-9.
The non chromaffin paraganglioma of the orbit is a relatively rare tumor. To our knowledge only 25 cases have been reported in the world literature. We report on the case of a 39-year-old woman who was treated surgically for the removal of an orbital paraganglioma 10 years ago. She had complained of proptosis and her right eyeball was slightly displaced upwards and laterally. A transcranial operation was performed and the tumor, located medically and weighing 9'5 grs., was completely removed; it was encapsulated. 10 years after this total excision there was no evidence of recurrence. From a histological point of view the tumor cells closely resembled those of paragangliomas of the carotid body and glomus jugulare.
眼眶非嗜铬性副神经节瘤是一种相对罕见的肿瘤。据我们所知，世界文献中仅报道了25例。我们报告一例39岁女性病例，她于10年前接受了手术切除眼眶副神经节瘤的治疗。她曾诉说有眼球突出，其右眼眼球略向上和向外移位。进行了经颅手术，肿瘤位于内侧，重9.5克，被完整切除；它有包膜。在完全切除后的10年里，没有复发的迹象。从组织学角度来看，肿瘤细胞与颈动脉体和颈静脉球副神经节瘤的细胞非常相似。
