Mena J, Bowen J C, Hollier L H
Department of Surgery, Ochsner Clinic, New Orleans, La. 70121.
Surgery. 1993 Jul;114(1):107-11.
The occurrence of an intercarotid paraganglioma and a paraganglioma in an anatomic distribution away from the head and neck in the same patient is rare. We have treated a patient with this combination of tumors and report this unusual case with the purpose of reviewing the paraganglion system. We endeavor to clarify the confusion that exists by use of the terms chemodectoma, glomus tumors, nonchromaffin paragangliomas, and pheochromocytoma and to present a rational nomenclature based on their ontogeny.
A computer-generated list of articles on this subject was obtained, and all articles relative to this rare combination of tumors were reviewed.
We found 31 other cases. Functional intercarotid paragangliomas are extremely rare, with only five cases having been reported.
All hypertensive patients who are found to have an intercarotid paraganglioma should be investigated for a functional tumor. Family members should also be made aware of their probabilities of having these tumors because a familial trend has been documented in certain cases.
同一患者在颈动脉旁出现副神经节瘤,且在头颈部以外的解剖部位也出现副神经节瘤的情况极为罕见。我们治疗了一位患有这两种肿瘤的患者,并报告这一罕见病例,旨在对副神经节系统进行回顾。我们努力厘清因使用化学感受器瘤、球瘤、非嗜铬性副神经节瘤和嗜铬细胞瘤这些术语而产生的混淆,并基于其个体发生情况提出合理的命名法。
通过计算机生成关于该主题的文章列表,并对所有与这种罕见肿瘤组合相关的文章进行了回顾。
我们还发现了其他31例病例。具有功能的颈动脉旁副神经节瘤极为罕见,仅有5例报告。
所有被发现患有颈动脉旁副神经节瘤的高血压患者都应接受功能性肿瘤的检查。家庭成员也应了解他们患这些肿瘤的可能性,因为在某些病例中已记录到家族性倾向。