Walker P J, Fagan P A
Department of Otolaryngology, St. Vincent's Hospital, Darlinghurst, Sydney, Australia.
Am J Otol. 1993 May;14(3):306-8.
The third reported case of a pheochromocytoma-like syndrome attributable to a catecholamine-secreting paraganglioma arising within the pterygopalatine fossa is documented. The 25-year-old, female subject was found to have raised levels of urinary catecholamines. At another center, a large vascular tumor was identified at lateral rhinotomy. Biopsy confirmed the diagnosis of paraganglioma. Tumor removal by a Fisch type-C approach to the sphenoid, parasellar region, and pterygopalatine fossa was complete and recovery uneventful.
本文记录了第三例归因于翼腭窝内发生的分泌儿茶酚胺的副神经节瘤所致的嗜铬细胞瘤样综合征。该25岁女性患者被发现尿儿茶酚胺水平升高。在另一中心,经鼻侧切开术发现一个大的血管性肿瘤。活检确诊为副神经节瘤。采用 Fisch C型入路对蝶骨、鞍旁区域和翼腭窝进行肿瘤切除,手术完整,恢复顺利。