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鼻腔及鼻咽副神经节瘤

Nasal and nasopharyngeal paraganglioma.

作者信息

Kuhn J A, Aronoff B L

机构信息

Department of Surgery, Baylor University Medical Center, Dallas, Texas 75246.

出版信息

J Surg Oncol. 1989 Jan;40(1):38-45. doi: 10.1002/jso.2930400110.

Abstract

Paragangliomas of the nasal cavity and nasopharynx should be classified according to the presumed origin from the nasal, jugulotympanic, vagal, or ciliary paraganglion because of the substantial differences in clinical behavior and operative management. This paper presents the ninth published case of a primary nasal paraganglioma and reviews the previously reported cases. Primary nasal paragangliomas are generally localized, although the potential for local invasion is well documented. Malignancy or functional activity has not been described. Complete excision is curative. Jugulotympanic, vagal, and ciliary paragangliomas with extension into the nasopharynx or nasal cavity are typically more advanced at the time of diagnosis and require complete evaluation by computed tomography and arteriography to determine the tumor extent. The operative approach is dependant on the extent of tumor invasion. Irradiation and tumor embolization have been useful for unresectable or partially excised tumors.

摘要

鼻腔和鼻咽副神经节瘤应根据其假定起源于鼻、颈静脉鼓室、迷走或睫状副神经节进行分类,因为它们在临床行为和手术处理上存在显著差异。本文介绍了第九例已发表的原发性鼻副神经节瘤病例,并回顾了先前报道的病例。原发性鼻副神经节瘤一般局限,但局部侵袭的可能性已有充分记录。尚未有恶性或功能性活动的描述。完整切除可治愈。延伸至鼻咽或鼻腔的颈静脉鼓室、迷走和睫状副神经节瘤在诊断时通常病情更晚,需要通过计算机断层扫描和动脉造影进行全面评估以确定肿瘤范围。手术入路取决于肿瘤侵袭的范围。放疗和肿瘤栓塞对不可切除或部分切除的肿瘤有用。

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