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海绵窦内的海绵状血管瘤

Cavernous hemangiomas in the cavernous sinus.

作者信息

Shi J, Hang C, Pan Y, Liu C, Zhang Z

机构信息

Department of Neurosurgery, Jinling Hospital, School of Medicine College of Nanjing University, The People's Republic of China.

出版信息

Neurosurgery. 1999 Dec;45(6):1308-13; discussion 1313-4. doi: 10.1097/00006123-199912000-00006.

Abstract

OBJECTIVE

Cavernous hemangiomas located within the cavernous sinus are rare vascular tumors that are very difficult to remove because of severe intraoperative bleeding. The purpose of this study was to analyze the clinical, neuroimaging, and pathological features and the surgical treatment of these tumors.

METHODS

Ten patients with cavernous hemangiomas in the cavernous sinus who were surgically treated from August 1985 to October 1997, in our hospital, were retrospectively studied.

RESULTS

Among the 10 patients, total tumor removal was performed in four cases, partial removal in two cases, and tumor biopsies in four cases. The four patients who underwent total tumor removal experienced uneventful postoperative courses, with no postoperative neurological deficits for one patient, no new neurological deficits for two patients, and complete ophthalmoplegia and diminished sensation in the distribution of Cranial Nerve V1 for one patient. The two patients who underwent partial removal developed complete ophthalmoplegia and diminished sensation in the distribution of Cranial Nerve V1 after surgery, and one of them experienced contralateral paralysis. All four patients who underwent tumor biopsies experienced severe intraoperative tumor bleeding; one exhibited Cranial Nerve III, IV, and VI injuries after surgery.

CONCLUSION

The features of prominent hyperintensity in T2-weighted scans, with well-defined borders in enhancing magnetic resonance imaging scans, or marked enhancement in computed tomographic and magnetic resonance imaging scans, with no tumor blush in angiographic analyses, facilitate the diagnosis of these tumors. These tumors can be divided into two subgroups on the basis of intraoperative findings and pathological features. We do not recommend division and piecemeal removal of the tumor during surgery if the main supplies of the tumor have not been interrupted.

摘要

目的

海绵窦内海绵状血管瘤是罕见的血管性肿瘤,由于术中出血严重,很难切除。本研究旨在分析这些肿瘤的临床、神经影像学和病理特征以及外科治疗方法。

方法

对1985年8月至1997年10月在我院接受手术治疗的10例海绵窦海绵状血管瘤患者进行回顾性研究。

结果

10例患者中,4例行肿瘤全切,2例行部分切除,4例行肿瘤活检。4例肿瘤全切患者术后恢复顺利,1例无术后神经功能缺损,2例无新的神经功能缺损,1例出现完全性眼肌麻痹及三叉神经眼支分布区感觉减退。2例部分切除患者术后出现完全性眼肌麻痹及三叉神经眼支分布区感觉减退,其中1例出现对侧瘫痪。4例肿瘤活检患者术中均出现严重肿瘤出血,1例术后出现动眼神经、滑车神经和展神经损伤。

结论

T2加权扫描呈明显高信号、增强磁共振成像扫描边界清晰或计算机断层扫描和磁共振成像扫描明显强化且血管造影分析无肿瘤染色等特征有助于这些肿瘤的诊断。根据术中发现和病理特征,这些肿瘤可分为两个亚组。如果肿瘤的主要供血未被阻断,我们不建议在手术中对肿瘤进行分割和逐块切除。

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