Bonduelle M
Rev Neurol (Paris). 1978 Aug-Sep;134(8-9):503-6.
Three cases of the disease are reported by the author. Clinical observations showed them to be unilateral lesions, not affecting the Vth motor nerve fibers, and without any other neurological disorder. The lesions had been present for 16, 8, and 2 years respectively. Radiography and tomography of the petrous bone was normal, as was tomodensitometry in the third case. The three patient developed a syndrome with dysesthesia and hypoesthesia after several weeks or months, and this remained fairly constant. In such cases which progress over a long period of time, in which there is no anatomical basis, and in which no aetiology can be found, the only conclusions to be drawn are clinical ones: that this is a true syndrome of chronic isolated sensory neuropathy of the trigeminal nerve.
作者报告了3例该疾病。临床观察显示，这些病例均为单侧病变，不影响第V对运动神经纤维，且无任何其他神经功能障碍。病变分别已存在16年、8年和2年。岩骨的X线摄影和体层摄影均正常，第三例的计算机体层密度测定也正常。3例患者在数周或数月后出现感觉异常和感觉减退综合征，且该症状相当稳定。在这类病程较长、无解剖学基础且找不到病因的病例中，唯一能得出的结论就是临床结论：这是一种真正的三叉神经慢性孤立性感觉神经病综合征。
