Department of Ophthalmology, Osaka Medical College, Osaka, Japan.
Medicine (Baltimore). 2021 Apr 9;100(14):e25062. doi: 10.1097/MD.0000000000025062.
Enlargemento of the medial rectus is the most predominant factor of compressive optic neuropathy (CON) in Graves' disease. This case report indicates that CON could develop only from the hypertrophic superior levator and superior rectus (SL/SR) muscle in a patient with poorly controlled Graves' disease, and described the possible risk of FT3-thyrotoxicosis with a prominent goiter to develop the current rare case with a review of the literature.
A 66-year-old woman undergoing endocrine management of hyperthyroidism with prominent goiter visited the Department of Ophthalmology due to right-eye upper-eyelid retraction.
At initial presentation, the right and left margin reflex distance-1 (MRD-1) was 3.2 mm and 2.1 mm, respectively, and no proptosis or visual dysfunction was observed. Despite insufficient hormonal regulation, she refused to undergo goiter removal. The upper eyelid retraction gradually worsened to 7.7 mm of MRD-1, followed by the onset of 20 prism diopters (PD) of the right hypertropia, resulting in right-eye CON after 6 months. Her free thyroxin level was 3.88 ng/dl and free triiodothyronine was 24.90 pg/ml. Computed tomography and magnetic resonance imaging showed only SL/SR enlargement in the right orbit.
Intravenous steroid and radiation therapy resulted in visual improvement; however, a prominent upper eyelid retraction and 35PD of hypertropia remained in her right eye. Orbital decompression, upper retraction repair, and superior rectus recession were performed to prevent the recurrence of CON and correct any disfigurement.
The combination of conventional intravenous steroid pulse therapy, radiotherapy, and orbital decompression was effective, and no recurrence was observed for more than 1.5-years postoperatively.
Enlargement of the SL/SR muscle complex may independently induce the CON. We believe that strict attention should be paid to patients with triiodothyronine thyrotoxicosis with progressive eyelid retraction and hypertropia.
在格雷夫斯病中,内侧直肌的扩大是压迫性视神经病变(CON)的最主要因素。本病例报告表明,在甲状腺功能亢进症控制不佳的患者中,CON 仅可能由肥大的上直肌和上直肌(SL/SR)肌肉引起,并描述了 FT3 毒性甲状腺功能亢进伴明显甲状腺肿的可能风险,同时对该罕见病例进行了文献复习。
一位 66 岁的女性因甲状腺功能亢进伴明显甲状腺肿正在接受内分泌治疗,她因右眼上眼睑回缩而就诊于眼科。
右眼和左眼的眶上缘距离-1(MRD-1)分别为 3.2mm 和 2.1mm,未观察到眼球突出或视觉功能障碍。尽管激素调节不足,她仍拒绝进行甲状腺肿切除术。上眼睑回缩逐渐恶化至 7.7mm 的 MRD-1,随后出现右眼 20 棱镜度(PD)的斜视,6 个月后右眼发生 CON。游离甲状腺素水平为 3.88ng/dl,游离三碘甲状腺原氨酸为 24.90pg/ml。计算机断层扫描和磁共振成像仅显示右侧眼眶中 SL/SR 增大。
静脉注射类固醇和放射治疗后视力有所改善;然而,右眼仍存在明显的上眼睑回缩和 35PD 的斜视。进行了眼眶减压、上眼睑回缩修复和上直肌后退术,以防止 CON 复发和纠正任何畸形。
常规静脉内类固醇脉冲疗法、放疗和眼眶减压联合治疗有效,术后超过 1.5 年未复发。
SL/SR 肌肉复合体的增大可能会独立引起 CON。我们认为,对于三碘甲状腺原氨酸毒性甲状腺功能亢进伴进行性眼睑回缩和斜视的患者应给予严格关注。