Iváñez V, Moreno M
Servicio de Neurología, Hospital Universitario La Paz, Universidad Autónoma, Madrid, España.
Rev Neurol. 1999;28(5):485-7.
The appearance of trigeminal neuralgia in infancy is exceptional. Trigeminal neuralgia as the only manifestation of a Chiari malformation is also infrequent. We present the case of a patient with a Chiari type I malformation in which the only symptom was the presence of trigeminal neuralgia since infancy. We have found no similar cases in the literature.
A 39 year old man with no significant clinical history complained of brief, recurrent episodes of pain in the right maxillary region, compatible with trigeminal neuralgia since the age of eight. The frequency, duration and intensity of these episodes had progressively increased. The only unusual finding on physical examination was a sluggish right corneal reflex. Cranial MR showed descent of the cerebellar tonsils to below the level of the posterior arch of the atlas, together with slight descent of the brainstem. These findings are characteristic of a Chiari type I malformation. The symptoms rapidly disappeared when treatment was started with carbamazepine.
In exceptional cases, trigeminal neuralgia may present in infancy and be the only manifestation of a Chiari malformation.
婴儿期出现三叉神经痛极为罕见。三叉神经痛作为Chiari畸形的唯一表现也不常见。我们报告一例自婴儿期起唯一症状为三叉神经痛的I型Chiari畸形患者。我们在文献中未发现类似病例。
一名39岁男性,无显著临床病史,自8岁起就抱怨右上颌区域反复出现短暂疼痛,符合三叉神经痛症状。这些发作的频率、持续时间和强度逐渐增加。体格检查中唯一异常发现是右侧角膜反射迟钝。头颅磁共振成像显示小脑扁桃体降至寰椎后弓水平以下,同时脑干略有下移。这些表现是I型Chiari畸形的特征。开始使用卡马西平治疗后症状迅速消失。
在罕见情况下,三叉神经痛可能在婴儿期出现,并且是Chiari畸形的唯一表现。