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伴有蛛网膜下腔出血的大脑镰硬脑膜动静脉畸形

[Dural arteriovenous malformation in the falx with subarachnoid hemorrhage].

作者信息

Agawa M, Kohno T, Sogabe K

机构信息

Department of Neurosurgery, Nakamura City Hospital.

出版信息

No Shinkei Geka. 1991 Sep;19(9):841-5.

PMID:1944792
Abstract

A case of falx dural arteriovenous malformation was reported. A 62 year old man was admitted to Nakamura City Hospital on August 15, 1989, with severe headache as his chief complaint. On admission, his consciousness was lethargic. CT scan showed subarachnoid hemorrhage with ventricular perforation and hematoma of the corpus callosum. Angiograms demonstrated a dural arteriovenous malformation (DAVM) in the frontal falx, which was fed by bilateral middle meningeal arteries and the left anterior falx artery and drained into the superior sagittal sinus via the dural vein. Bifrontal craniotomy was performed. At first, bilateral middle meningeal arteries were coagulated, and the frontoparietal dura was excised widely. Then, the falx was cut at the crista galli. The DAVM was found in the falx, including a vascular sac embedded in the brain tissue. The DAVM was coagulated as much as possible. Carotid angiograms revealed complete disappearance of the DAVM, 4 months after the operation. Although angiograms performed after only one month still showed a small residual DAVM. On reviewing the literature we found only 5 patients with the DAVM in the falx. In 6 cases including our own, intracranial hemorrhage occurred in 4 cases (3 cases were subarachnoid hemorrhage). Vascular sacs were seen in 4 cases, and drainage to the pial vein was noted in 3 cases. It seemed to be rare that the DAVM drained into the dural vein. In our particular case, operative findings showed the DAVM drained into the dural vein without the pial vein, and intracranial hemorrhage was attributed to rupture of the vascular sac.

摘要

报道了一例大脑镰硬脑膜动静脉畸形病例。一名62岁男性于1989年8月15日因严重头痛为主诉入住中村市医院。入院时,他意识嗜睡。CT扫描显示蛛网膜下腔出血伴脑室穿孔和胼胝体血肿。血管造影显示额部大脑镰存在硬脑膜动静脉畸形(DAVM),由双侧脑膜中动脉和左侧大脑镰前动脉供血,并通过硬脑膜静脉引流至上矢状窦。进行了双侧额部开颅手术。首先,凝固双侧脑膜中动脉,广泛切除额顶部硬脑膜。然后,在鸡冠处切断大脑镰。在大脑镰中发现了DAVM,包括一个嵌入脑组织的血管囊。尽可能多地凝固DAVM。术后4个月颈动脉血管造影显示DAVM完全消失。尽管仅1个月后进行的血管造影仍显示有一小部分残留的DAVM。查阅文献发现仅有5例大脑镰DAVM患者。包括我们自己的病例在内的6例中,4例发生颅内出血(3例为蛛网膜下腔出血)。4例可见血管囊,3例注意到向软脑膜静脉引流。DAVM引流至硬脑膜静脉似乎较为罕见。在我们这个特殊病例中,手术所见显示DAVM经硬脑膜静脉引流而无软脑膜静脉,颅内出血归因于血管囊破裂。

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