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通过X线平片检测到的复发性钙化性脊膜瘤。

Recurrent calcified spinal meningioma detected by plain radiograph.

作者信息

Doita M, Harada T, Nishida K, Marui T, Kurosaka M, Yoshiya S

机构信息

Department of Orthopedic Surgery, Meiwa Hospital, Nishinomiya, Japan.

出版信息

Spine (Phila Pa 1976). 2001 Jun 1;26(11):E249-52. doi: 10.1097/00007632-200106010-00005.

Abstract

STUDY DESIGN

A case report of a patient presenting with a rare calcified spinal meningioma that recurred and became symptomatic 33 years after initial surgery was performed.

OBJECTIVES

To demonstrate a calcified recurrent spinal meningioma visible on a plain radiograph. The present case is discussed in conjunction with a review of previous cases of calcified spinal meningioma.

SUMMARY OF BACKGROUND DATA

Meningioma is a common spinal tumor that has a favorable prognosis if resected completely. Microscopic calcification is frequently found in spinal meningiomas because of psammoma bodies. However, calcified meningiomas in the spinal canal that can be detected on a plain radiograph are uncommon. To the authors' knowledge, there have been no previous reports of recurrent spinal meningioma with calcification visible on a plain radiograph.

METHODS

A patient experienced difficulty in walking and was diagnosed as having a spinal meningioma. Laminectomies and a total tumor excision were performed. Histologically, the tumor was diagnosed as a psammomatous meningioma. The tumor recurred and became symptomatic 33 years after the initial operation. The tumor was detected on a plain radiograph, appearing as a calcified tumor at the same thoracic level as the site of the initial operation. The recurrent tumor was completely removed, and a histologic examination showed huge psammoma bodies with calcification, but without ossification.

RESULTS

Preoperative paraplegia improved after the surgery, and she was able to walk with a crutch. The patient was discharged from the hospital.

CONCLUSIONS

The recurrent psammomatous meningioma contained clusters of calcified psammoma bodies, resulting in a hard tumor that was visible on a plain radiograph.

摘要

研究设计

一份病例报告,讲述一名患者患有罕见的钙化性脊髓脑膜瘤,在初次手术后33年复发并出现症状。

目的

展示在X线平片上可见的钙化性复发性脊髓脑膜瘤。结合既往钙化性脊髓脑膜瘤病例回顾对本病例进行讨论。

背景资料总结

脑膜瘤是一种常见的脊髓肿瘤,若能完全切除则预后良好。由于砂粒体,脊髓脑膜瘤中常可见微观钙化。然而,能在X线平片上检测到的椎管内钙化性脑膜瘤并不常见。据作者所知,此前尚无关于在X线平片上可见钙化的复发性脊髓脑膜瘤的报道。

方法

一名患者出现行走困难,被诊断为患有脊髓脑膜瘤。实施了椎板切除术及肿瘤全切术。组织学检查显示,该肿瘤被诊断为砂粒体型脑膜瘤。肿瘤在初次手术后33年复发并出现症状。在X线平片上检测到肿瘤,表现为与初次手术部位相同胸段水平的钙化性肿瘤。复发性肿瘤被完全切除,组织学检查显示有巨大的伴有钙化的砂粒体,但无骨化。

结果

术后术前的截瘫症状有所改善,她能够借助拐杖行走。患者出院。

结论

复发性砂粒体型脑膜瘤包含成簇的钙化砂粒体,形成了一个在X线平片上可见的坚硬肿瘤。

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