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[巨大融合性脑膜瘤的成功切除]

[A successful removal of huge confluence meningioma].

作者信息

Suzuki S, Mizoi K, Kato S, Suzuki J

机构信息

Division of Neurosurgery, Tohoku University School of Medicine, Sendai, Japan.

出版信息

No Shinkei Geka. 1988 Mar;16(3):289-94.

PMID:3374747
Abstract

A rare case of huge confluence meningioma with many kinds of venous collaterals is presented. A 58-year-old female was admitted because of severe headache and gait disturbance. An enhanced CT (computerized tomography) scan demonstrated a homogeneous spherical high density mass in the region of the posterior falco-tentorial junction adjacent to the internal occipital crest. Cerebral angiograms showed (1) the occluded confluence sinuum and compensatory venous collaterals, (2) venous drainage through the persistent falcial sinus, which was rare in an adult, from the straight sinus into the superior sagittal sinus (SSS), (3) venous drainage through diploic veins and emissary veins into scalp veins. The tumor including the confluence sinuum was totally removed via a combined bioccipital and suboccipital craniectomy. The confluence sinuum was invaded and occluded by the tumor. The tumor was histologically diagnosed as a fibroblastic meningioma. Post-operative angiogram showed a formation of the new venous channel which is located between the posterior part of the SSS and the lateral part of right transverse sinus. The origin of this new venous pathway was thought to be congenital presence of a "latent" dural venous channel. After ventriculoperitoneal shunting, the patient was discharged without any neurological deficits. A follow-up angiogram one year and two months after discharge showed that the channel become dilated and the venous collaterals seen before surgery disappeared probably due to the change of balance of venous pressure. The venous drainage pattern seemed to become resembling the normal variant type in which the SSS drains into the right transverse sinus, and left sinus was hypoplastic.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文报告一例罕见的伴有多种静脉侧支的巨大融合性脑膜瘤病例。一名58岁女性因严重头痛和步态障碍入院。增强CT扫描显示,在枕内嵴附近的后颅窝小脑幕交界处有一个均匀的球形高密度肿块。脑血管造影显示:(1)窦汇闭塞及代偿性静脉侧支;(2)经持续存在的大脑镰窦(在成人中罕见)从直窦引流至上矢状窦的静脉引流;(3)经板障静脉和导静脉引流至头皮静脉的静脉引流。通过联合双侧枕部和枕下颅骨切除术,完整切除包括窦汇在内的肿瘤。窦汇被肿瘤侵犯并闭塞。肿瘤组织学诊断为纤维母细胞型脑膜瘤。术后血管造影显示,在矢状窦后部和右侧横窦外侧之间形成了一条新的静脉通道。这条新静脉通道的起源被认为是“潜在”硬脑膜静脉通道的先天性存在。在进行脑室腹腔分流术后,患者出院时无任何神经功能缺损。出院后1年零2个月的随访血管造影显示,该通道扩张,术前可见的静脉侧支可能因静脉压力平衡的改变而消失。静脉引流模式似乎变得类似于正常变异型,即上矢状窦引流至右侧横窦,左侧窦发育不良。(摘要截断于250字)

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