1Jiro Suzuki Memorial Gamma House, Furukawa Seiryo Hospital, Osaki.
2Department of Pathology, Tohoku Kosai Hospital, Sendai.
J Neurosurg. 2022 Dec 23;139(1):165-175. doi: 10.3171/2022.11.JNS221535. Print 2023 Jul 1.
Gamma Knife radiosurgery (GKRS) is a powerful tool for the management of arteriovenous malformations; however, newly formed mass lesions resembling cavernous malformations are a rare late complication of GKRS. In this retrospective study, the authors tried to clarify the unique histological features of these mass lesions.
The authors retrospectively reviewed the clinical course of 889 patients who had undergone GKRS for arteriovenous malformations at their institute from 1991 to 2021. Among the 848 patients who had been followed up periodically with neuroradiological imaging, 37 developed a mass lesion mimicking a cavernous malformation and underwent surgical removal of the lesion. The median volume of the original nidus was 3.7 cm3 (range 0.07-30.5 cm3), and the median prescription dose was 21 Gy (range 12-25 Gy). The histological characteristics and radiological and clinical features of the 37 patients were investigated.
Histological examination showed an organized hematoma and a structure termed "retiform endothelial hyperplasia" (RFEH) consisting of endothelium forming multiple lumen-like vascular channels mimicking cavernous malformations but lacking the subendothelial connective tissue that forms the typical vascular wall structure found in cavernous angioma and capillary telangiectasia. RFEH was detected a median of 10.8 years (range 3.2-27.4 years) after GKRS. Neuroimaging showed hematoma surrounded by massive brain edema in all 37 patients. Symptoms caused by mass effect of the lesion and perifocal edema worsened relatively rapidly but completely disappeared after surgery. No recurrence or morbidity occurred after the surgery.
The delayed formation of RFEH that is mimicking a cavernous malformation neuroradiologically but is histologically distinct from a vascular malformation is a potential complication of GKRS. Its progressive clinical course suggests that surgical removal should be considered for symptomatic patients and/or patients with an apparent radiological mass sign.
伽玛刀放射外科(GKRS)是治疗动静脉畸形的有力工具;然而,新形成的类似于海绵状畸形的肿块样病变是 GKRS 的罕见迟发性并发症。在这项回顾性研究中,作者试图阐明这些肿块样病变的独特组织学特征。
作者回顾性分析了 1991 年至 2021 年在他们所在机构接受 GKRS 治疗动静脉畸形的 889 例患者的临床过程。在 848 例定期接受神经影像学随访的患者中,有 37 例出现了类似于海绵状畸形的肿块样病变,并进行了病变的手术切除。原始病灶的中位数体积为 3.7cm3(范围 0.07-30.5cm3),中位数处方剂量为 21Gy(范围 12-25Gy)。研究了 37 例患者的组织学特征、影像学和临床特征。
组织学检查显示,一个有序的血肿和一种被称为“网状内皮细胞增生(RFEH)”的结构,由形成多个类似于海绵状畸形的管腔样血管通道的内皮细胞组成,但缺乏形成典型血管壁结构的下内皮结缔组织,而这种结构存在于海绵状血管畸形和毛细血管扩张症中。RFEH 在 GKRS 后中位数 10.8 年(范围 3.2-27.4 年)被发现。所有 37 例患者的神经影像学均显示血肿周围伴有巨大的脑水肿。由于病变和周围水肿的占位效应引起的症状相对迅速恶化,但在手术后完全消失。手术后无复发或并发症发生。
在影像学上类似于海绵状畸形但在组织学上与血管畸形不同的 RFEH 的延迟形成是 GKRS 的一种潜在并发症。其进行性临床过程表明,对于有症状的患者和/或有明显影像学肿块征象的患者,应考虑手术切除。