Thompson H S
Trans Am Ophthalmol Soc. 1977;75:587-626.
Adie's syndrome is a disease of unknown etiology. We known where the damage is, and which nerves are involved. We even know something of how the nerves react after the damage is done, but we don't known what causes the primary injury. The first step in working a jigsaw puzzle is to getall of the pieces right side up and take a good look at them. Some of the jigsaw pieces handled in this paper are listed below. Some of them are new observations; many of them are old concepts, partly modified and partly made secure by new facts. 1. Not all "tonic pupils" are due to "Adie's syndrome"; some are due to local injury and some to a generalized peripheral neuropathy (Table II). 2. All patients should have serologic tests for shyphilis. In this series one in six had positive serology. 3. The incidence of Adie's syndrome in Iowa in the early 1970's was approximately 4.7 per 100,000 population per year. 4. The prevalence of Adie's syndrome, therefore, was approximately 2 per 1000. 5. The mean age of onset of Adie's syndrome was about 32.2 years (Figure 1A). 6. The sex ratio was 2.6 females to each male. 7. Right eyes and left eyes were involved at approximately the same rate (Figure 2). 8. The incidence of second eye involvement in unilateral cases was about 4% per year during the first decade of the disease (Figure 18). 9. If this rate of second eye involvement (4% per year) persists during subsequent decades, then most Adie's pupils will eventually become bilateral. 10. The incidence of Adie's syndrome in a largely caucasian patient group is independent of iris color (Figure 4). 11. Only 10% of patients with Adie's syndrome had completely normal muscle stretch reflexes. 12. The muscle stretch reflexes in the arms were just as frequently imparied as those in th elegs, but the degree of impariment tended to be more severe in the ankles and triceps. 13. When there was any light reaction remaining in an Adie's pupil, a segmental paralysis of the sphincter muscle could be seen. 14. The near reaction of the pupil was often segmental and frequently involved segments which did not respond to light. 15. The segmental paralysis to light was randomly distributed around the sphincter (Figure 6B). 16. There was some tendency for the sphincter palsy to gradually become worse. This progression was also random (Figure 8). 17. Almost all patients with Adie's syndrome had an accommodative paresis at the time of onset. 18. Reading glasses given to a patient with a fresh Adie's pupil were soon discarded as accommodation recovered (Figure 9). 19. Accomodative effort induced an astigmatism in about half of the eyes with Adie's--presumably the result of a segmental palsy of the ciliary muscle. 20. Tonicity of accommodation was present in about 1/2 of the eyes with Adie's, making it difficut for the patient to maintain a steady level of ciliary muscle tone. 21. An occasional patient complained of brow ache from ciliary spasm with near work. 22. In most patients with Adie's syndrome the ciliary muscle was supersensitive to pilocarpine 0...
艾迪综合征是一种病因不明的疾病。我们知道损伤发生在哪里,以及哪些神经受到了影响。我们甚至对神经在损伤发生后的反应也有所了解,但我们不知道是什么导致了原发性损伤。玩拼图游戏的第一步是把所有的拼图块都正面朝上放好,然后好好看看它们。本文涉及的一些拼图块如下。其中一些是新的观察结果;许多是旧概念,部分经过修改,部分因新事实而得到确证。1. 并非所有“强直性瞳孔”都由“艾迪综合征”引起;有些是由局部损伤引起,有些是由全身性周围神经病变引起(表二)。2. 所有患者都应进行梅毒血清学检测。在这个系列中,六分之一的患者血清学呈阳性。3. 20世纪70年代初,爱荷华州艾迪综合征的发病率约为每年每10万人口4.7例。4. 因此,艾迪综合征的患病率约为千分之二。5. 艾迪综合征的平均发病年龄约为32.2岁(图1A)。6. 男女比例为2.6比1。7. 右眼和左眼受累的比例大致相同(图2)。8. 在疾病的第一个十年中,单侧病例中对侧眼受累的发病率约为每年4%(图18)。9. 如果在随后的几十年中这种对侧眼受累的发生率(每年4%)持续存在,那么大多数艾迪瞳孔最终将变为双侧性。10. 在一个主要为白种人的患者群体中,艾迪综合征的发病率与虹膜颜色无关(图4)。11. 只有10%的艾迪综合征患者的肌肉牵张反射完全正常。12. 手臂的肌肉牵张反射与腿部的肌肉牵张反射受损频率相同,但踝关节和三头肌处的受损程度往往更严重。13. 当艾迪瞳孔仍有任何光反应时,可以看到瞳孔括约肌的节段性麻痹。14. 瞳孔的近反射通常是节段性的,且常常涉及对光无反应的节段。15. 对光的节段性麻痹在括约肌周围随机分布(图6B)。16. 括约肌麻痹有逐渐加重的趋势。这种进展也是随机的(图8)。17. 几乎所有艾迪综合征患者在发病时都有调节麻痹。18. 给患有新出现的艾迪瞳孔的患者佩戴的阅读眼镜,随着调节功能的恢复很快就被丢弃了(图9)。19. 大约一半患有艾迪综合征的眼睛,调节努力会诱发散光——推测是睫状肌节段性麻痹的结果。20. 约一半患有艾迪综合征的眼睛存在调节紧张,这使得患者难以维持稳定的睫状肌张力水平。21. 偶尔有患者抱怨近距离工作时因睫状肌痉挛而眉痛。22. 在大多数艾迪综合征患者中,睫状肌对毛果芸香碱0...