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原发性中枢神经系统血管肉瘤:两例病例报告。

Primary central nervous system angiosarcoma: two case reports.

作者信息

Hackney James R, Palmer Cheryl Ann, Riley Kristen O, Cure Joel K, Fathallah-Shaykh Hassan M, Nabors Louis B

机构信息

Division of Neuropathology, University of Alabama at Birmingham, PD6A 175, Birmingham, AL, 35294, USA.

出版信息

J Med Case Rep. 2012 Aug 21;6:251. doi: 10.1186/1752-1947-6-251.

Abstract

INTRODUCTION

Primary angiosarcoma of the brain is extremely rare; only 15 cases have been reported in adults over the last 25 years.

CASE PRESENTATIONS

We describe two cases of primary angiosarcoma of the brain that are well characterized by imaging, histopathology, and immunohistochemistry. Case 1: our first patient was a 35-year-old woman who developed exophthalmos. Subtotal resection of a left extra-axial retro-orbital mass was performed. Case 2: our second patient was a 47-year-old man who presented to our facility with acute visual loss, word-finding difficulty and subtle memory loss. A heterogeneously-enhancing left sphenoid wing mass was removed. We also review the literature aiming at developing a rational approach to diagnosis and treatment, given the rarity of this entity.

CONCLUSIONS

Gross total resection is the standard of care for primary angiosarcoma of the brain. Adjuvant radiation and chemotherapy are playing increasingly recognized roles in the therapy of these rare tumors.

摘要

引言

原发性脑血管肉瘤极为罕见;在过去25年中,成人中仅报告了15例。

病例报告

我们描述了两例原发性脑血管肉瘤病例,通过影像学、组织病理学和免疫组织化学对其进行了充分表征。病例1:我们的首例患者是一名35岁女性,出现眼球突出。对左侧轴外眶后肿物进行了次全切除。病例2:我们的第二例患者是一名47岁男性,因急性视力丧失、找词困难和轻微记忆力减退前来我院就诊。切除了左侧蝶骨嵴不均匀强化肿物。鉴于该实体的罕见性,我们还回顾了文献,旨在制定合理的诊断和治疗方法。

结论

全切除是原发性脑血管肉瘤的治疗标准。辅助放疗和化疗在这些罕见肿瘤的治疗中发挥着越来越重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e94/3459733/950c7820bbc6/1752-1947-6-251-6.jpg

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