Pokharel Dipesh, Siatkowski R Michael
College of Medicine, University of Oklahoma, Oklahoma City, OK 73104, USA.
J AAPOS. 2004 Jun;8(3):286-7. doi: 10.1016/j.jaapos.2004.01.014.
The Chiari malformations are characterized by herniation of posterior fossa contents through the foramen magnum. Chiari I malformation is currently defined as ectopia of the cerebellar tonsils more than 5 mm below the foramen magnum. Extension of the cerebellar tonsils up to 3 mm may be found in the normal population. Although Chiari malformations are congenital, symptoms often do not manifest until the third and fourth decades of life, or even later. Patients usually present with headache, lower cranial nerve palsies, downbeat nystagmus, ataxia, or dissociated anesthesia of the trunk and extremities. Definitive diagnosis is made by magnetic resonance imaging (MRI), which shows the compressed tonsils extending through the foramen magnum into the cervical subarachnoid space. One of the rare presenting signs of Chiari I malformations is acquired esotropia with a divergence insufficiency pattern. We report such a case in which the initial neuroimaging showed tonsillar herniation, but of insufficient magnitude to meet diagnostic criteria for Chiari I malformation. When the strabismus recurred after initially successful eye muscle surgery, follow-up scan showed progressive tonsillar herniation.
Chiari畸形的特征是后颅窝内容物通过枕骨大孔疝出。Chiari I型畸形目前定义为小脑扁桃体异位至枕骨大孔下方超过5毫米处。在正常人群中可能会发现小脑扁桃体向下延伸达3毫米。尽管Chiari畸形是先天性的,但症状通常直到生命的第三和第四个十年甚至更晚才会出现。患者通常表现为头痛、下颅神经麻痹、下跳性眼球震颤、共济失调或躯干及四肢感觉分离性麻木。通过磁共振成像(MRI)做出明确诊断,MRI显示受压的扁桃体通过枕骨大孔延伸至颈蛛网膜下腔。Chiari I型畸形罕见的表现体征之一是获得性内斜视伴散开功能不全模式。我们报告了这样一例病例,最初的神经影像学检查显示扁桃体疝出,但程度不足以满足Chiari I型畸形的诊断标准。当最初成功的眼部肌肉手术后斜视复发时,随访扫描显示扁桃体疝出逐渐加重。