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原发性眼眶间叶性软骨肉瘤:病例报告及文献复习

Primary orbital mesenchymal chondrosarcoma: case report and review of the literature.

作者信息

Herrera Angel, Ortega Cesar, Reyes Gervith, Alvarez Miguel Angel, Tellez Daniela

机构信息

Department of Surgical Oncology, Instituto Nacional de Cancerología, Mexico City, Mexico.

出版信息

Case Rep Med. 2012;2012:292147. doi: 10.1155/2012/292147. Epub 2012 Jun 18.

Abstract

Orbital mesenchymal chondrosarcoma is a very uncommon lesion of the bone and extraskeletal tissue. To our knowledge, approximately 30 cases have been described. We present the case of a 52-year-old male who presented with a history of progressive proptosis and chemosis of the right eye caused by an orbital tumor. He underwent exenteration of the right orbit, and the histological examination revealed a mesenchymal orbital chondrosarcoma. This paper attempts to describe a rare entity that should be considered in the differential diagnosis of calcified orbital lesions, especially in young adults. Complete removal of the tumor is the mainstay of treatment, but adjuvant radiation therapy and chemotherapy should be considered.

摘要

眼眶间叶性软骨肉瘤是一种非常罕见的骨与骨骼外组织病变。据我们所知,大约已报道了30例病例。我们报告一例52岁男性患者,其因眼眶肿瘤出现右眼进行性眼球突出和结膜水肿病史。他接受了右眼眶内容剜除术,组织学检查显示为间叶性眼眶软骨肉瘤。本文试图描述一种罕见的疾病实体,在钙化眼眶病变的鉴别诊断中应予以考虑,尤其是在年轻成年人中。肿瘤的完整切除是主要治疗方法,但也应考虑辅助放疗和化疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/681d/3385622/b531d250a425/CRIM2012-292147.001.jpg

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