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[慢性包裹性脑内血肿合并海绵状血管瘤:病例报告及文献复习]

[Chronic encapsulated intracerebral hematoma associated with cavernous angioma: case report and review of the literature].

作者信息

Okuno S, Hisanaga M, Miyasaki A, Tsunoda S, Sakaki T

机构信息

Department of Neurosurgery, Senboku National Hospital.

出版信息

No Shinkei Geka. 1993 Jul;21(7):655-9.

PMID:8327061
Abstract

We reported a case of chronic encapsulated intracerebral hematoma associated with cavernous angioma. A 71-year old female was admitted with a history of frontal headaches at intervals of about 3 months for the last one year. Plain CT scan showed a round mass of heterogeneous high density in the left medial frontal lobe. The outer surface of the mass was enhanced with contrast material. MRI demonstrated the mass as a high signal intensity on T1-weighted image and low intensity with laminated structure on T2-weighted image. MR angiogram depicted the mass as a mottled high signal intensity. The left internal carotid artery angiogram revealed no abnormal shadows and vessels. These findings suggested some form of a thrombus although its underlying pathogenesis was unclear. On January 20, 1992, a bifrontal craniotomy was performed. A whitish well-demarcated mass was seen in the left cingulate gyrus through a small corticotomy. We could not identify any branches feeding the mass. The cross-section of the mass disclosed a uniform thrombus encapsulated by a thick wall. Histological studies of the wall confirmed a cavernous angioma within the outer collagenous layers. Chronic encapsulated hematoma, which was first reported by Hirsh in 1981, has represented a separate entity and 25 such cases have been documented in the literature. These reports suggested that the compression and/or destruction of the surrounding tissue caused by the hemorrhage would mask the existence of the cavernous angioma or vascular malformation. If an encapsulated hematoma were encountered during an operation, surgeons should pay attention not to overlook the residual capsule encompassing the cavernous angioma or vascular malformation.

摘要

我们报告了一例与海绵状血管瘤相关的慢性包裹性脑内血肿病例。一名71岁女性因在过去一年中每隔约3个月出现一次前额头痛的病史入院。平扫CT扫描显示左额叶内侧有一个圆形的不均匀高密度肿块。肿块外表面在注入造影剂后有强化。MRI显示该肿块在T1加权图像上为高信号强度,在T2加权图像上为低信号强度且有分层结构。磁共振血管造影显示该肿块为斑驳的高信号强度。左侧颈内动脉血管造影未显示异常阴影和血管。这些发现提示存在某种形式的血栓,尽管其潜在发病机制尚不清楚。1992年1月20日,进行了双额开颅手术。通过一个小的皮质切口,在左扣带回中可见一个界限清楚的白色肿块。我们未发现为该肿块供血的任何分支。肿块的横截面显示为一个被厚壁包裹的均匀血栓。对壁的组织学研究证实外层胶原层内有海绵状血管瘤。慢性包裹性血肿由赫什于1981年首次报道,已成为一个独立的实体,文献中已记录了25例此类病例。这些报告表明,出血对周围组织的压迫和/或破坏会掩盖海绵状血管瘤或血管畸形的存在。如果在手术中遇到包裹性血肿,外科医生应注意不要忽视包裹海绵状血管瘤或血管畸形的残留包膜。

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