Eide P K, Stubhaug A
Department of Neurosurgery, The National Hospital, University of Oslo, Norway.
Neurosurgery. 1998 Sep;43(3):462-72; discussion 472-4. doi: 10.1097/00006123-199809000-00036.
This study was undertaken to examine the pathophysiological mechanisms of trigeminal neuralgia and the mechanisms underlying pain relief after percutaneous retrogasserian glycerol rhizolysis (PRGR).
Quantitative examination of sensory and pain perception was performed in the trigger area and the contralateral nonpainful facial skin area for 39 patients with trigeminal neuralgia who had been previously treated with PRGR and for 14 non-surgically treated patients. In a prospective study, 9 of the 14 patients were examined before and 4 to 6 weeks after PRGR.
In the trigger area of patients who had been previously treated with PRGR for trigeminal neuralgia, we demonstrated increased temperature and tactile thresholds in pain-free patients and in patients with paroxysmal or continuous pain. Abnormal temporal summation of pain (characterized by progressive increases in pain intensity, with radiation of pain and aftersensation) was present in patients with paroxysmal or continuous pain but not in pain-free patients. In the trigger area of non-surgically treated patients with trigeminal neuralgia, we demonstrated significantly increased temperature and tactile thresholds and the presence of abnormal temporal summation of pain. The prospective study showed that pain relief after PRGR was associated with normalization of abnormal temporal summation of pain, without increased sensory loss.
Partial deafferentation, with impairment of thin (C/Adelta) and thick (Abeta) fiber-mediated sensations and abnormal temporal summation of pain, is present in the trigger area of patients with trigeminal neuralgia. Relief of pain after PRGR depends on the normalization of abnormal temporal summation of pain, which is independent of general impairment of sensory perception. Assessment of the temporal summation of pain may serve as an important tool to record central neuronal hyperexcitability, which may play a key role in the pathophysiological changes in trigeminal neuralgia.
本研究旨在探讨三叉神经痛的病理生理机制以及经皮半月神经节甘油注射毁损术(PRGR)后疼痛缓解的机制。
对39例曾接受PRGR治疗的三叉神经痛患者以及14例未接受手术治疗的患者,在触发区和对侧无痛面部皮肤区域进行感觉和疼痛感知的定量检查。在一项前瞻性研究中,对14例患者中的9例在PRGR术前及术后4至6周进行了检查。
在曾接受PRGR治疗三叉神经痛的患者的触发区,我们发现无痛患者以及阵发性或持续性疼痛患者的温度和触觉阈值均升高。阵发性或持续性疼痛患者存在异常的疼痛时间总和现象(表现为疼痛强度逐渐增加、疼痛放射及余痛),而无痛患者则无此现象。在未接受手术治疗的三叉神经痛患者的触发区,我们发现温度和触觉阈值显著升高且存在异常的疼痛时间总和现象。前瞻性研究表明,PRGR术后疼痛缓解与异常疼痛时间总和现象的正常化相关,且感觉丧失未增加。
三叉神经痛患者的触发区存在部分传入神经阻滞,伴有细纤维(C/Adelta)和粗纤维(Abeta)介导的感觉受损以及异常的疼痛时间总和现象。PRGR术后疼痛缓解取决于异常疼痛时间总和现象的正常化,这与感觉感知的总体损害无关。疼痛时间总和现象的评估可能是记录中枢神经元兴奋性过高的重要工具,而中枢神经元兴奋性过高可能在三叉神经痛的病理生理变化中起关键作用。