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眶顶局限性原发性颅内尤文肉瘤。病例报告。

Localized primary intracranial Ewing's sarcoma of the orbital roof. Case report.

作者信息

Alvarez-Berdecia A, Schut L, Bruce D A

出版信息

J Neurosurg. 1979 Jun;50(6):811-3. doi: 10.3171/jns.1979.50.6.0811.

Abstract

A rare case of a primary Ewing's sarcoma arising from the intracranial portion of the right orbital roof is presented. Clinical presentation was that of a rapidly growing tender exostosis, associated with headaches. History indicated that the tumor may have been present for more than 1 year. Skull x-rays showed marked diastasis of the coronal suture and a "mottled" appearance on the right frontal bone suggestive of a sarcoma. Bone scan further confirmed the presence of a malignant bone tumor. Computerized tomography scan showed the intracranial extension of the tumor and a follow-up scan allowed us to see the response of the tumor to therapy. Only two other cases with details as to intracranial localization were found in the literature.

摘要

本文报告一例罕见的起源于右眶顶颅内部分的原发性尤因肉瘤。临床表现为快速生长的压痛性外生骨疣,并伴有头痛。病史表明肿瘤可能已存在超过1年。颅骨X线片显示冠状缝明显增宽,右侧额骨呈“斑驳”样外观,提示肉瘤。骨扫描进一步证实存在恶性骨肿瘤。计算机断层扫描显示肿瘤向颅内扩展,随访扫描使我们能够观察到肿瘤对治疗的反应。文献中仅发现另外两例有颅内定位详细信息的病例。

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