Serous retinal detachment secondary to bilateral choroidal osteoma successfully treated with subscleral sclerectomy: A case report

Satoko Fujimoto , Kazuichi Maruyama , Takuya Shunto , Kohji Nishida
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Abstract

Purpose

To report a case of bilateral choroidal osteoma successfully treated with subscleral sclerectomy for secondary serous retinal detachment (SRD).

Observations

A 52-year-old Japanese woman first diagnosed with Vogt-Koyanagi-Harada disease and treated with steroids for 9 years was referred to our clinic. SRD in both eyes recurred frequently and was uncontrolled with adalimumab subcutaneous injections and oral cyclosporine, in addition to steroids. A yellowish-to-orange, slightly elevated subretinal lesion was observed superior to the macular and inferotemporal regions of the right eye and superior to the macular and temporal regions of the left eye without any inflammation. Swept-source optical coherence tomography (OCT) revealed SRD in the fovea and a mass under the retinal pigment epithelium (RPE) in the macular area of both eyes. Indocyanine green angiography (ICGA) demonstrated hypocyanescence corresponding to the mass area under the RPE, with dilation of the dominant vortex veins. Ultrasonography revealed a hyperechogenic mass in the posterior wall of both eyes with deeper acoustic shadows, and computed tomography (CT) detected calcifications in the posterior wall of both eyes. A bilateral choroidal osteoma was diagnosed, and the superior SRD of her left eye increased toward the fovea without any evidence of choroidal neovascularization during follow-up. Therefore, subscleral sclerectomy (4 × 4 mm2 sclerectomy under the scleral flap) was performed at three sites at the equators in the upper temporal, upper nasal, and lower temporal quadrants of her left eye. Immediately after surgery, SRD resolved dramatically. As the foveal SRD of her right eye also increased after two months, the same surgery was performed, and it worked successfully.

Conclusions and Importance

Choroidal osteoma can cause severe SRD that cannot be controlled with medication. Although further studies are needed, subscleral sclerectomy may be an effective treatment for the resolution of subretinal fluid secondary to choroidal osteoma by improving choroidal circulation congestion.
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巩膜下巩膜切除术成功治疗双侧脉络膜骨瘤继发的浆液性视网膜脱离1例。
目的:报告一例巩膜下巩膜切除术治疗继发性浆液性视网膜脱离(SRD)成功的双侧脉络膜骨瘤。观察:一名52岁的日本女性首次被诊断为Vogt-Koyanagi-Harada病,并接受类固醇治疗9年。双眼SRD经常复发,并且在阿达木单抗皮下注射和口服环孢素以及类固醇治疗下不受控制。在右眼黄斑和颞下区域上方和左眼黄斑和颞下区域上方观察到黄至橙色,轻度升高的视网膜下病变,未见任何炎症。扫描源光学相干断层扫描(OCT)显示双眼中央凹有SRD,黄斑区视网膜色素上皮(RPE)下有肿块。吲哚菁绿血管造影(ICGA)显示与RPE下肿块区相对应的低青色,主要旋涡静脉扩张。超声检查发现双眼后壁有高回声肿块伴较深的声影,CT检查发现双眼后壁有钙化。诊断为双侧脉络膜骨瘤,随访期间左眼上侧SRD向中央凹方向增加,未见脉络膜新生血管形成。因此,在左眼上颞、上鼻部和下颞象限赤道处的三个部位行巩膜下巩膜切除术(巩膜瓣下4 × 4 mm2巩膜切除术)。手术后,SRD立即得到显著缓解。由于她的右眼中央凹SRD在两个月后也增加了,因此进行了同样的手术,并取得了成功。结论和重要性:脉络膜骨瘤可引起严重的SRD,不能用药物控制。虽然需要进一步的研究,但通过改善脉络膜循环充血,巩膜下巩膜切除术可能是解决脉络膜骨瘤继发视网膜下积液的有效治疗方法。
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来源期刊
CiteScore
2.40
自引率
0.00%
发文量
513
审稿时长
16 weeks
期刊介绍: The American Journal of Ophthalmology Case Reports is a peer-reviewed, scientific publication that welcomes the submission of original, previously unpublished case report manuscripts directed to ophthalmologists and visual science specialists. The cases shall be challenging and stimulating but shall also be presented in an educational format to engage the readers as if they are working alongside with the caring clinician scientists to manage the patients. Submissions shall be clear, concise, and well-documented reports. Brief reports and case series submissions on specific themes are also very welcome.
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