Sawamura Y, Tashiro K, Shima K, Moriwaka F, Abe H
Department of Neurology, Hokkaido University School of Medicine, Sapporo, Japan.
No To Shinkei. 1988 Sep;40(9):863-8.
The differential diagnosis of trigeminal neuropathy is quite challenging because there is a significant variety of causes for the disorder. We reviewed our cases of trigeminal neuropathy by studying first the initial manifestations in order to evaluate their underlying disorders. Sixty-four patients with trigeminal neuropathy came to our Out-Patients clinic. We have excluded from our analysis any patients with atypical pain, facial migraine, nasal sinusitis, pain from inflammation of dental pulp or facial bones, and pretrigeminal neuralgia. In 53 cases (83%) we identified the causes; 35 of them were cases of symptomatic trigeminal neuritis and 18 were trigeminal neuralgia while, in the remaining 11 cases, no definitive causative disorder was identified. Among the 35 patients with symptomatic neuritis, 10 cases were found to have malignant neoplasms including 5 cases of squamous cell carcinoma, 6 had a virus infection, 5 had traumatic origin, 4 had multiple sclerosis, 2 exhibited Tolosa-Hunt syndrome, 2 had MCTD, and there were single cases of sarcoidosis, serpentine aneurysm, cavernous sinus thrombosis, maxillary cyst and trigeminal neurinoma. The remaining 11 cases of neuritis whose causes were undetermined showed clinical features similar to trigeminal sensory neuropathy, an analogue of Bell's palsy, a benign self-limiting condition. Since the cases shared symptoms of impairment of taste, and, occasionally, of facial palsy, vestibular insufficiency, hearing disturbance, hypoglossal palsy or signs of cerebellar lesion, we strongly suspected a virus origin.(ABSTRACT TRUNCATED AT 250 WORDS)
三叉神经病变的鉴别诊断颇具挑战性,因为该病症的病因种类繁多。我们通过首先研究初始表现来回顾我们的三叉神经病变病例,以便评估其潜在疾病。64例三叉神经病变患者前来我们的门诊就诊。我们在分析中排除了任何患有非典型疼痛、面部偏头痛、鼻窦炎、牙髓或面部骨骼炎症引起的疼痛以及三叉神经前神经痛的患者。在53例(83%)病例中我们确定了病因;其中35例为症状性三叉神经炎,18例为三叉神经痛,而在其余11例中,未确定明确的致病疾病。在35例症状性神经炎患者中,发现10例患有恶性肿瘤,包括5例鳞状细胞癌,6例有病毒感染,5例有创伤性病因,4例有多发性硬化症,2例表现为托洛萨-亨特综合征,2例有混合性结缔组织病,还有结节病、蜿蜒状动脉瘤、海绵窦血栓形成、上颌囊肿和三叉神经鞘瘤各1例。其余11例病因未明的神经炎表现出与三叉神经感觉神经病变相似的临床特征,类似于贝尔麻痹,是一种良性自限性疾病。由于这些病例有味觉障碍症状,偶尔还有面瘫、前庭功能不全、听力障碍、舌下神经麻痹或小脑病变体征,我们强烈怀疑其病因是病毒。(摘要截选至250词)