Suarez Mallory K, Martin Timothy J, Ong Sally S
Department of Ophthalmology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
J Vitreoretin Dis. 2024 May 6;8(4):466-470. doi: 10.1177/24741264241251582. eCollection 2024 Jul-Aug.
To report the retinal findings in a patient with autosomal recessive spastic ataxia of Charlevoix-Saguenay. A case was evaluated. A 16-year-old male patient with a known diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay was referred for evaluation of retinal hypermyelination given its frequent association with the condition. The patient was asymptomatic with a best-corrected visual acuity of 20/20. Optical coherence tomography of the peripapillary retinal nerve fiber layer (RNFL) showed bilateral thickening in each eye (average thicknesses: 180 µm, right eye; 177 µm, left eye). An examination showed no myelinization of the RNFL. Most studies to date describe RNFL thickening secondary to hypermyelination as a characteristic finding in autosomal recessive spastic ataxia of Charlevoix-Saguenay. This case provides evidence that this thickening may be a result of hypertrophy rather than hypermyelination. Further investigation is needed to define the pathophysiologic cause of RNFL thickening in autosomal recessive spastic ataxia of Charlevoix-Saguenay.
报告一名患有常染色体隐性遗传性夏勒沃魁 - 萨格奈痉挛性共济失调患者的视网膜检查结果。对一例病例进行了评估。一名已知诊断为常染色体隐性遗传性夏勒沃魁 - 萨格奈痉挛性共济失调的16岁男性患者因视网膜高髓鞘化与该疾病频繁相关而被转诊进行评估。该患者无症状,最佳矫正视力为20/20。视乳头周围视网膜神经纤维层(RNFL)的光学相干断层扫描显示每只眼睛均有双侧增厚(平均厚度:右眼180 µm;左眼177 µm)。检查显示RNFL无髓鞘化。迄今为止,大多数研究将继发于高髓鞘化的RNFL增厚描述为常染色体隐性遗传性夏勒沃魁 - 萨格奈痉挛性共济失调的特征性表现。该病例提供了证据表明这种增厚可能是肥大而非高髓鞘化的结果。需要进一步研究以确定常染色体隐性遗传性夏勒沃魁 - 萨格奈痉挛性共济失调中RNFL增厚的病理生理原因。