Prayson Richard A, Yoder Brian J
Department of Anatomic Pathology, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
Ann Diagn Pathol. 2007 Feb;11(1):22-6. doi: 10.1016/j.anndiagpath.2006.03.004.
Mesial temporal sclerosis (MTS) is the most common cause of medically intractable temporal lobe epilepsy. Histologic findings include hippocampal atrophy with neuronal loss in the dentate, CA1, and CA3/CA4 regions with gliosis. The conventional treatment of patients with intractable epilepsy secondary to MTS has been surgical excision. Gamma knife radiotherapy (GKR) has recently been suggested as a less invasive alternative to surgery. To date, the histologic changes that occur in this setting after GKR have not been well described. The clinicopathologic features of 4 patients with MTS who received GKR and underwent subsequent surgical resection or autopsy were retrospectively reviewed. The study group is composed of 4 patients (3 women, 1 men) with ages 55, 48, 22, and 20 years, respectively, at the time of GKR. There were 2 patients who had a history of infantile febrile seizures, and 2 who had a central nervous infection during infancy. All 4 patients had a long-standing (13-36 years) history of temporal lobe seizures resistant to medical management. Imaging studies, electroencephalogram, and surgical specimens all confirmed the diagnosis of MTS. The oldest of the 4 patients died 1 month after receiving GKR, presumably because of post-gamma knife persistent seizure complications. The postmortem neuropathology on this patient was unremarkable for any radiation effect changes but showed evidence of MTS. The remaining 3 patients underwent surgical resection for persistent seizures at 18, 22, and 20 months, respectively, post-gamma knife. These 3 surgical specimens showed variable degrees of radiation effect changes in the temporal lobe, hippocampus, and amygdala, including chronic (lymphocytes and macrophages) perivascular inflammation (3/3), vascular sclerosis (3/3), foci of edema with necrosis (3/3; extensive in 2 patients), reactive astrocytosis (3/3), microglial proliferation (1/3), and microcalcifications (1/3). Patients with MTS who underwent GKR can develop typical radiation changes over time. Treatment of individuals with MTS via GKR may not always be adequate in controlling seizures. Radiation therapy effect may contribute to persistent seizures after GKR in some patients with MTS.
内侧颞叶硬化(MTS)是药物难治性颞叶癫痫最常见的病因。组织学表现包括海马萎缩,齿状回、CA1区以及CA3/CA4区神经元缺失并伴有胶质增生。对于继发于MTS的难治性癫痫患者,传统治疗方法是手术切除。最近,有人提出伽玛刀放射治疗(GKR)可作为一种侵入性较小的手术替代方案。迄今为止,GKR治疗后出现的组织学变化尚未得到充分描述。我们回顾性分析了4例接受GKR治疗并随后接受手术切除或尸检的MTS患者的临床病理特征。研究组由4例患者组成(3例女性,1例男性),接受GKR治疗时年龄分别为55岁、48岁、22岁和20岁。其中2例患者有婴儿期热性惊厥病史,2例在婴儿期有中枢神经系统感染史。所有4例患者均有长期(13 - 36年)的颞叶癫痫病史,药物治疗无效。影像学检查、脑电图及手术标本均确诊为MTS。4例患者中年龄最大的在接受GKR治疗1个月后死亡,可能是由于伽玛刀治疗后持续性癫痫发作并发症所致。该患者的尸检神经病理学检查未发现任何放射效应改变,但显示有MTS的证据。其余3例患者在伽玛刀治疗后分别于18个月、22个月和20个月因癫痫持续发作接受了手术切除。这3份手术标本显示颞叶、海马和杏仁核有不同程度的放射效应改变,包括慢性(淋巴细胞和巨噬细胞)血管周围炎症(3/3)、血管硬化(3/3)、伴有坏死的水肿灶(3/3;2例广泛)、反应性星形细胞增生(3/3)、小胶质细胞增生(1/3)和微钙化(1/3)。接受GKR治疗的MTS患者随着时间推移可出现典型的放射改变。通过GKR治疗MTS患者可能并不总能有效控制癫痫发作。放射治疗效应可能导致部分MTS患者在GKR治疗后癫痫持续发作。