Choroidal Nevus with Choroidal Detachment Simulating Intraocular Melanoma - Imageand Pathology Studies

Chun-Ju Lin, Jane-Ming Lin, Wen-Lu Chen, P. Tien, Y. Tsai
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Abstract

Purpose: Malignant uveal melanoma is the most common primary intraocular malignant tumors in adults. Choroidal detachment and choroidal nevus may be confused with choroidal tumors. We report a case of choroidal nevus and rhegmatogenous retinal detachment (RD) complicated with macular pucker and choroidal detachment simulating intraocular melanoma. Method: Interventional case report. Results: A 59-year-old woman complained of visual disturbances and superior temporal visual defect for 1 month in the left eye. Funduscopy revealed macular pucker with lower RD and an elevated lesion with pigment mottling in the nasal-lower quadrant. The optical coherence tomography (OCT) scan showed macular pucker with subretinal fluid. B scan ultrasonography showed low to moderate internal reflectivity. Fluorescein angiography demonstrated irregular pattern of mixed hypo- and hyperfluorescence in the elevated lesion and dye pooling on the posterior pole. Computed tomography (CT) revealed an intraocular enhancing mass. Positron-emission tomography/computed tomography (PET/CT) showed no abnormal 18F-fluoro-2-deoxyglucose uptake. Because the evidence of malignancy was not solid and the patient also sought to improve her vision, the small gauge vitrectomy was performed. A retinal break was found on the slope of choroidal detachment intraoperatively. Specimens were taken through the retinal break. Internal limiting membrane peeling, air-fluid exchange, focal laser around the retinal break and C3F8 tamponade were done. The postoperative magnetic resonance imaging (MRI) showed no clue of enlargement. Due to mild hyperintensity on T1-weighted imaging, choroidal melanoma was suspected by the radiologist. However, pathology showed no malignancy. The retina was attached and the retinal break was sealed on the slope during 34-month follow up. Conclusion: Choroidal nevus and choroidal hemorrhage with detachment should be carefully differentiated from choroidal melanoma. Apart from CT and MRI, PET/CT can assess both anatomical morphology and cell metabolism in one single examination. Long term follow-up is necessary.
脉络膜痣伴脉络膜脱离模拟眼内黑色素瘤的影像与病理研究
目的:恶性葡萄膜黑色素瘤是成人最常见的原发性眼内恶性肿瘤。脉络膜脱离和脉络膜痣可能与脉络膜肿瘤混淆。我们报告一例脉络膜痣和孔源性视网膜脱离(RD)并发黄斑皱褶和脉络膜脱离模拟眼内黑色素瘤。方法:介入病例报告。结果:一名59岁女性主诉左眼视力障碍及颞上视力缺损1个月。眼底镜检显示黄斑皱褶与下RD和高病变与色素斑驳在鼻-下象限。光学相干断层扫描(OCT)显示黄斑皱,视网膜下积液。B超示内反射率低至中等。荧光素血管造影显示凸起病灶呈不规则混合低荧光和高荧光,后极呈染色池状。计算机断层扫描(CT)显示一个眼内增强肿块。正电子发射断层扫描/计算机断层扫描(PET/CT)未显示异常的18f -氟-2-脱氧葡萄糖摄取。由于恶性肿瘤的证据不明确,并且患者也寻求改善她的视力,因此进行了小尺寸玻璃体切除术。术中在脉络膜脱离斜坡处发现视网膜断裂。通过视网膜裂口取标本。内限定膜剥离、气液交换、视网膜裂口周围激光聚焦、C3F8填塞。术后MRI未见肿大。由于t1加权成像轻度高信号,放射科医生怀疑脉络膜黑色素瘤。病理未见恶性肿瘤。在34个月的随访中,视网膜附着并在斜坡上封闭视网膜断裂。结论:脉络膜痣及脉络膜出血伴脱离应与脉络膜黑色素瘤鉴别。除了CT和MRI, PET/CT可以在一次检查中同时评估解剖形态和细胞代谢。长期随访是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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