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颅骨膜窦:15例患者的诊断与治疗考量

Sinus pericranii: diagnostic and therapeutic considerations in 15 patients.

作者信息

Gandolfo Carlo, Krings Timo, Alvarez Hortensia, Ozanne Augustin, Schaaf Meike, Baccin Carlos E, Zhao Wen-Yuan, Lasjaunias Pierre

机构信息

Service de Neuroradiologie Diagnostique et Thérapeutique, Hôpital de Bicetre, 78 rue du General Leclerc, 94275, Le Kremlin-Bicêtre, Paris, France.

出版信息

Neuroradiology. 2007 Jun;49(6):505-14. doi: 10.1007/s00234-007-0211-7. Epub 2007 Feb 7.

DOI:10.1007/s00234-007-0211-7
PMID:17285338
Abstract

INTRODUCTION

Sinus pericranii (SP) is a rare, usually asymptomatic condition characterized by a large communication between the intra- and the extracranial venous drainage pathways in which blood may circulate bidirectionally through dilated veins of the skull. We describe our diagnostic and therapeutic experience with SP, with a special focus on the vascular analysis of digital subtraction angiography (DSA).

METHODS

DSA images of 15 patients were evaluated with regard to the delay in opacification of the scalp vessels, the absence or distortion of the superficial cortical veins in the vicinity of the SP, the drainage patterns of the superior sagittal sinus, and the degree of maturation of the venous outlets of the brain. SP were classified either as "dominant", if the main stream of contrast flow used the SP to drain the brain bypassing usual venous outlets, or as "accessory", if only a small part of the venous outflow occurred through the extradiploic vessels.

RESULTS

All patients presented with a nonpulsatile, soft-tissue mass. The lesion was on the midline in 14 of 15 patients, frontal in 12 patients, and parietal in 2 patients. In 13 patients, associated intracranial venous anomalies were present, eight of which were developmental venous anomalies. Seven patients had a dominant SP, and eight an accessory SP.

CONCLUSION

SP can be considered the cutaneous sign of an underlying venous anomaly. If treatment is contemplated, analysis of the drainage pattern of the SP has to be performed. Treatment should be avoided in dominant SP or if its accessory role constitutes the only collateral pathway of an underlying venous anomaly.

摘要

引言

颅骨膜窦(SP)是一种罕见的、通常无症状的疾病,其特征是颅内和颅外静脉引流途径之间存在大的交通,血液可通过颅骨扩张的静脉双向循环。我们描述了我们对SP的诊断和治疗经验,特别关注数字减影血管造影(DSA)的血管分析。

方法

对15例患者的DSA图像进行评估,观察头皮血管造影剂延迟显影情况、SP附近浅表皮质静脉的缺失或扭曲、上矢状窦的引流模式以及脑静脉出口的成熟程度。如果对比剂主流通过SP绕过正常静脉出口引流大脑,则将SP分类为“优势型”;如果只有一小部分静脉血流通过板障外血管流出,则分类为“附属型”。

结果

所有患者均表现为非搏动性软组织肿块。15例患者中14例病变位于中线,12例位于额部,2例位于顶叶。13例患者存在相关颅内静脉异常,其中8例为发育性静脉异常。7例患者为优势型SP,8例为附属型SP。

结论

SP可被视为潜在静脉异常的皮肤征象。如果考虑治疗,必须对SP的引流模式进行分析。对于优势型SP或其附属作用构成潜在静脉异常唯一侧支通路的情况,应避免治疗。

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