Suppr超能文献

一名儿童的家族性多中心副神经节瘤

Familial multicentric paragangliomas in a child.

作者信息

Ophir D

机构信息

Department of Otolaryngology, Meir Hospital, Kfar Saba, Israel.

出版信息

J Laryngol Otol. 1991 May;105(5):376-80. doi: 10.1017/s0022215100116056.

Abstract

A 12-year-old girl presented with bilateral carotid-body paragangliomas and a unilateral jugular paraganglioma. The tumours were surgically removed. This is a rare combination of tumours in any patient and previously unreported in a child of this age. Her father died of a cerebellar astrocytoma and her mother underwent surgical removal of a large mediastinal paraganglioma. The association of astrocytoma with familial paragangliomas has never been documented. The literature on the epidemiology and inheritance pattern of familial paragangliomas is reviewed. The need for thorough pre-operative evaluation of the patient and close follow-up of family members is stressed.

摘要

一名12岁女孩患有双侧颈动脉体副神经节瘤和单侧颈静脉副神经节瘤。这些肿瘤通过手术切除。这种肿瘤组合在任何患者中都很罕见,在这个年龄段的儿童中此前未见报道。她的父亲死于小脑星形细胞瘤,她的母亲接受了巨大纵隔副神经节瘤的手术切除。星形细胞瘤与家族性副神经节瘤的关联从未有过记录。本文回顾了家族性副神经节瘤的流行病学和遗传模式的文献。强调了对患者进行全面术前评估以及对家庭成员进行密切随访的必要性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验