Gmeiner Matthias, Sonnberger Michael, Wurm Gabriele, Weis Serge
Division of Neurosurgery, Landes-Nervenklinik Wagner-Jauregg, Linz, Austria.
Clin Neurol Neurosurg. 2013 May;115(5):501-6. doi: 10.1016/j.clineuro.2012.12.009. Epub 2013 Jan 3.
Very few cases of arteriovenous malformations (AVMs) associated with gliomas were reported so far in the literature.
Here, we report a rare case of a glioblastoma with an AVM-like lesion and review the existing literature.
We report an unusual case of a 72-year old woman, who presented with a progressive history of aphasia, memory deficit, and headache. Initial MRI imaging was suggestive of a high-grade glioma for which a pterional craniotomy was performed. Intraoperatively, the lesion resembled a vascular malformation. Total extirpation of the lesion was verified by intraoperative MR imaging. Initial histopathological analysis revealed an AVM. Due to the discrepancy between the radiologic and histopathologic findings, the patient was monitored at close intervals. Two month later, multiple lesions were visible on MRI imaging, thus, supporting the diagnosis of malignant glioma. Therefore, after reinvestigating the histopathological sections and cutting the paraffin block in additional serial sections, in only 5% of the section a glioblastoma was discerned which was surrounded by an AVM-like lesion.
Gliomas are rarely found in association with AVMs and require accurate diagnostic evaluation and interpretation for adequate therapeutic interventions.
迄今为止,文献中报道的与胶质瘤相关的动静脉畸形(AVM)病例极少。
在此,我们报告一例罕见的伴有AVM样病变的胶质母细胞瘤病例,并回顾现有文献。
我们报告了一例不同寻常的病例,患者为一名72岁女性,有进行性失语、记忆缺陷和头痛病史。最初的MRI成像提示为高级别胶质瘤,为此进行了翼点开颅手术。术中,病变类似血管畸形。术中MRI成像证实病变已完全切除。最初的组织病理学分析显示为AVM。由于放射学和组织病理学结果存在差异,对患者进行了密切随访。两个月后,MRI成像上可见多个病变,从而支持恶性胶质瘤的诊断。因此,在重新检查组织病理学切片并将石蜡块切成更多连续切片后,仅在5%的切片中发现了一个被AVM样病变包围的胶质母细胞瘤。
胶质瘤很少与AVM相关联,需要进行准确的诊断评估和解读,以便采取适当的治疗干预措施。