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[眼眶副神经节瘤。附1例报告并文献复习]

[Orbital paraganglioma. Apropos of a case and review of the literature].

作者信息

Lockhart R, Auriol M, Fleuridas G, Chikhani L, Bertrand J C, Le Charpentier Y, Chiras J

机构信息

Institut de Stomatologie, Chirurgie Maxillo Faciale, Chirurgie Plastique de la Face, Groupe hospitalier Pitié Salprière, Paris.

出版信息

Rev Stomatol Chir Maxillofac. 1995;96(3):151-7.

PMID:7644892
Abstract

Paragangliomas are exceptional in the orbit. Among the 47 cases reported in the world literature more than 1/3 has been classified as alveolar soft part sarcoma. Diagnosis of paraganglioma was confirmed on the basis of pathology reports in only 10. We observed a case in a 46-year-old woman who presented with a tumour of the orbit. The histology examination and the ultrastructure determined by electron microscopy confirmed the diagnosis of paraganglioma. Characteristic histologic features are discussed together with a review of the literature.

摘要

眼眶副神经节瘤极为罕见。在世界文献报道的47例病例中,超过1/3曾被归类为肺泡软组织肉瘤。仅有10例根据病理报告确诊为副神经节瘤。我们观察了一例46岁患有眼眶肿瘤的女性病例。组织学检查及电子显微镜确定的超微结构均证实为副神经节瘤。本文结合文献回顾讨论了其特征性组织学表现。

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