Smith S A, Smith S E
Diabetes Day Centre, Guy's and St Thomas' Hospital Trust, London, UK.
J Neurol Neurosurg Psychiatry. 1999 Jan;66(1):48-51. doi: 10.1136/jnnp.66.1.48.
To develop a method for the detection of bilateral Horner's syndrome in patients with bilateral interruption of the cervical sympathetic pathway or widespread autonomic neuropathy.
Darkness pupil diameters and redilatation times during light reflexes have been recorded with infrared TV pupillometry in 65 healthy subjects, 47 patients with unilateral Horner's syndrome, and 20 patients with bilateral Horner's syndrome. The aetiologies of the last group were diabetic autonomic neuropathy (three cases), amyloidosis (four), pure autonomic failure (PAF) (four), dopamine-beta-hydroxylase deficiency (two), and one case each of hereditary sensory and autonomic neuropathy (HSAN) type III, carcinomatous sympathetic neuropathy, familial dysautonomia, multiple system atrophy, Anderson-Fabry disease, and anterior spinal artery thrombosis at C5,6 and one had had bilateral cervical sympathectomies.
Darkness diameters on the affected side were below normal in 12 patients with unilateral Horner's syndrome, the measurement yielding only 26% sensitivity for detection of the condition. By contrast, the time taken to reach three quarter recovery in the light reflex (T3/4) was abnormally prolonged (redilatation lag) in 33 of the same eyes. The measurement yielded 70% sensitivity and 95% specificity for detection of the condition. In 20 cases, diagnosed on clinical grounds as having bilateral Horner's syndrome of various aetiologies, pupil diameters were abnormally small on both sides in five and on one side in three patients. Fourteen of these patients had significant redilatation lag in both eyes, five patients in one eye, and one patient had it in neither eye. Measurement of redilatation lag was therefore a more sensitive diagnostic test than pupil diameter in both unilateral and bilateral Horner's syndrome.
Provided that the pupils are not tonic, bilateral Horner's syndrome can be diagnosed on the basis of redilatation lag. It occurs clinically in some generalised autonomic neuropathies and with interruption of the local sympathetic nerve supplies to the two eyes.
开发一种用于检测颈交感神经通路双侧中断或广泛自主神经病变患者双侧霍纳综合征的方法。
采用红外电视瞳孔测量法记录了65名健康受试者、47名单侧霍纳综合征患者和20名双侧霍纳综合征患者在暗光下的瞳孔直径以及光反射时的再扩张时间。最后一组患者的病因包括糖尿病自主神经病变(3例)、淀粉样变性(4例)、纯自主神经功能衰竭(PAF)(4例)、多巴胺-β-羟化酶缺乏症(2例),以及遗传性感觉和自主神经病变(HSAN)III型、癌性交感神经病变、家族性自主神经功能异常、多系统萎缩、安德森-法布里病各1例,还有1例因C5、6节段的脊髓前动脉血栓形成导致双侧霍纳综合征,另外1例曾接受双侧颈交感神经切除术。
12名单侧霍纳综合征患者患侧的暗光下瞳孔直径低于正常,该测量方法对该病的检测灵敏度仅为26%。相比之下,同一只眼睛中有33只在光反射时达到四分之三恢复所需的时间(T3/4)异常延长(再扩张延迟)。该测量方法对该病的检测灵敏度为70%,特异度为95%。在20例临床上诊断为各种病因导致的双侧霍纳综合征的患者中,5例双侧瞳孔直径异常小,3例单侧瞳孔直径异常小。这些患者中有14例双眼存在明显的再扩张延迟,5例单眼存在再扩张延迟,1例双眼均无再扩张延迟。因此,在单侧和双侧霍纳综合征中,测量再扩张延迟都是比瞳孔直径更敏感的诊断测试。
只要瞳孔不是强直性的,双侧霍纳综合征可根据再扩张延迟来诊断。临床上,它见于一些全身性自主神经病变以及双侧眼部局部交感神经供应中断的情况。