Chan T K, Demer J L
Department of Ophthalmology, University of California, Los Angeles, USA.
J AAPOS. 1999 Jun;3(3):143-50. doi: 10.1016/s1091-8531(99)70059-5.
Absence of an extraocular muscle was considered rare when demonstrable only by surgical exploration or necropsy. This study presents advances in orbital imaging to correlate clinical findings with absence of the superior oblique (SO) muscle.
We performed high-resolution coronal orbital imaging by magnetic resonance imaging (222 orbits) or computerized radiographic tomography (32 orbits) in 127 patients with strabismus. We reviewed the histories and ocular motility examinations in patients who had absence of 1 or both SO muscles. Findings were compared with patients who were clinically diagnosed with SO palsy but had demonstrable SO muscles on orbital imaging.
SO muscles were absent in 6 patients. All had histories suggesting congenital strabismus. In patients old enough for quantitative testing who had unilateral SO muscle absence, visual acuity was a least 20/25 in all and stereopsis was better than 80 arc/s in one. Three patients were orthotropic in primary position. Five patients with unilateral SO muscle absence had clinical findings variably consistent with SO palsy, whereas a sixth patient with Duane syndrome had clinically unsuspected bilateral SO muscle absence. Versions and patterns of hypertropia in patients with SO muscle absence overlapped findings of 20 patients with SO palsy but demonstrable SO muscles.
Imaging can frequently demonstrate absence of the SO muscle in patients with SO palsy. Such patients may have good vision and stereopsis and clinical findings indistinguishable from SO palsy without absence of the SO muscle. Orbital imaging should be considered in the evaluation of congenital SO palsy to facilitate planning of effective surgical correction.
仅通过手术探查或尸检才能证实眼外肌缺如的情况被认为较为罕见。本研究展示了眼眶成像技术的进展,以将临床发现与上斜肌(SO)缺如相关联。
我们对127例斜视患者进行了磁共振成像(222个眼眶)或计算机断层扫描(32个眼眶)的高分辨率冠状位眼眶成像。我们回顾了1条或2条SO肌缺如患者的病史和眼球运动检查结果。将这些发现与临床诊断为SO麻痹但眼眶成像显示SO肌存在的患者进行比较。
6例患者存在SO肌缺如。所有患者均有提示先天性斜视的病史。在年龄足够进行定量测试的单侧SO肌缺如患者中,所有人的视力至少为20/25,其中1人的立体视优于80弧秒。3例患者在第一眼位时眼位正。5例单侧SO肌缺如患者的临床表现与SO麻痹存在不同程度的一致性,而第6例患有杜安综合征的患者临床上未怀疑双侧SO肌缺如。SO肌缺如患者的上斜视度数和模式与20例SO麻痹但SO肌存在的患者的检查结果重叠。
成像检查常常能显示SO麻痹患者存在SO肌缺如。这类患者可能有良好的视力和立体视,其临床表现与不存在SO肌缺如的SO麻痹难以区分。在评估先天性SO麻痹时应考虑进行眼眶成像,以利于制定有效的手术矫正方案。