Kent Jerrod S, Makar Inas
Ivey Eye Institute, University of Western Ontario, London, Ont., Canada.
Case Rep Ophthalmol. 2012 May;3(2):230-5. doi: 10.1159/000339990. Epub 2012 Jul 24.
To report a case of bilateral Brown's syndrome with unilateral spontaneous resolution causing hypertropia and significant head tilt.
A 3 ½-year-old girl presented with bilateral typical Brown's syndrome and orthophoria in the primary position; she presented with unilateral resolution of right Brown's syndrome 6 months later, causing right hypertropia and gradually deteriorating left head tilt. She benefited from right superior rectus muscle recession to help correct her head posture.
This is the first report of a patient presenting with known bilateral Brown's syndrome with subsequent documented unilateral resolution causing a significant hypertropia of the resolved side and contralateral head tilt. Our case provides evidence in support of Clark and Noël's [Can J Ophthalmol 1993;28:213-216] hypothesis that patients who present with unilateral Brown's syndrome and contralateral inferior oblique muscle overaction might originally have had bilateral Brown's syndrome with spontaneous resolution of 1 side only.
报告一例双侧布朗综合征,其中一侧自发缓解,导致患侧上斜视和明显的头部倾斜。
一名3岁半女童初诊时表现为双侧典型布朗综合征且原在位正位视;6个月后右侧布朗综合征自发缓解,导致右侧上斜视和左侧头部倾斜逐渐加重。她接受了右眼上直肌后徙术,有助于纠正其头部姿势。
这是首例报告的已知双侧布朗综合征患者,随后记录到一侧自发缓解,导致缓解侧明显上斜视和对侧头部倾斜。我们的病例为克拉克和诺埃尔[《加拿大眼科杂志》1993年;28:213 - 216]的假说提供了证据,即表现为单侧布朗综合征和对侧下斜肌亢进的患者最初可能患有双侧布朗综合征,仅一侧自发缓解。