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动静脉畸形破裂继发急性自发性硬膜下血肿:一种罕见的病症。

Acute spontaneous subdural hematoma secondary to ruptured arteriovenous malformation: A rare entity.

作者信息

Kieu Hung Dinh, Le Tam Duc, Hoang Tan Minh

机构信息

Department of Surgery, Hanoi Medical University, Hanoi, Viet Nam.

Department of Neurosurgery and Spine Surgery, Hanoi Medical University Hospital, Hanoi, Viet Nam.

出版信息

Ann Med Surg (Lond). 2021 Jul 27;68:102613. doi: 10.1016/j.amsu.2021.102613. eCollection 2021 Aug.

Abstract

INTRODUCTION

Acute spontaneous subdural hematoma (ASSDH) due to ruptured arteriovenous malformation (AVM) is exceptional. There were only four reported cases. In this paper, we present a successful multimodality treatment of the ASSDH secondary to ruptured AVM.

CASE PRESENTATION

A 21-year-old healthy man with no history of trauma presented to our hospital with complaints of severe headache for 12 hours before admission. On examination, he was alert and oriented. He had no intracranial hypertension, meningismus, and neurological deficits. Computed tomography illustrated a right acute subdural hematoma 8mm in thickness with a 5mm midline shift and a right frontal intraparenchymal hemorrhage 40 × 25mm in size. Digital subtraction angiography showed a 2 × 3 cm right frontal AVM, Spetzler-Martin grade I. The feeding arteries were cortical branches of the right anterior cerebral artery, and drain veins were cortical veins. He received emergency preoperative embolization followed by hematoma evacuation and total excision of the malformation. His headache was relieved and disappeared after a week. No postoperative neurological deficits were reported.

CLINICAL DISCUSSION

Elective surgical resection of AVM after 4-6 weeks was preferred in patients with no risk factors of rebleeding. Emergent surgery was only indicated for significant mass effect or acute hydrocephalus. Preoperative embolization is helpful for the presence of intra-nidal or peri-nidal aneurysm, AVM with high grades, reducing intraoperative blood loss and occlusion of deep vessels.

CONCLUSION

ASSDH due to ruptured AVM is rare and easy to omit in clinical settings. Preoperative embolization and surgical excision are effective treatments.

摘要

引言

因动静脉畸形(AVM)破裂导致的急性自发性硬膜下血肿(ASSDH)极为罕见。仅报道过4例。在本文中,我们介绍了1例成功采用多模式治疗破裂AVM继发ASSDH的病例。

病例介绍

一名21岁无外伤史的健康男性因入院前12小时出现严重头痛而就诊于我院。体格检查时,他意识清醒、定向力正常。无颅内高压、颈项强直及神经功能缺损。计算机断层扫描显示右侧急性硬膜下血肿,厚度8mm,中线移位5mm,右侧额叶脑实质内出血,大小为40×25mm。数字减影血管造影显示右侧额叶有一个2×3cm的AVM,Spetzler-Martin分级为I级。供血动脉为右侧大脑前动脉的皮质分支,引流静脉为皮质静脉。他接受了急诊术前栓塞治疗,随后进行了血肿清除及畸形灶全切术。一周后其头痛缓解并消失。未报告术后神经功能缺损。

临床讨论

对于无再出血危险因素的患者,首选在4 - 6周后择期手术切除AVM。急诊手术仅适用于有明显占位效应或急性脑积水的情况。术前栓塞对于存在瘤巢内或瘤巢周围动脉瘤、高分级AVM、减少术中失血及闭塞深部血管有帮助。

结论

因AVM破裂导致的ASSDH罕见,在临床中容易被漏诊。术前栓塞及手术切除是有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43dd/8340043/f385351b017f/gr1a.jpg

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