Choroidal Effusion Mimicking Uveal Melanoma: A Novel Presentation of Idiopathic Systemic Capillary Leak Syndrome.

IF 0.9 Q4 OPHTHALMOLOGY
Ocular Oncology and Pathology Pub Date : 2021-12-01 Epub Date: 2021-09-21 DOI:10.1159/000512765
Beatrice Y Brewington, Srinivas Kondapalli, Shaili S Kothari, Samir V Parikh, Colleen M Cebulla
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引用次数: 3

Abstract

Background: Idiopathic systemic capillary leak syndrome (ISCLS, also known as Clarkson's disease) is a rare medical condition characterized by episodes of capillary endothelial cell dysfunction with leakage of fluid into the interstitial space resulting in severe hypotension, hemoconcentration, hypoalbuminemia, and generalized edema. Each episode can result in multiorgan failure due to systemic hypoperfusion.

Case presentation: We report a case of uveal effusion, mimicking uveal melanoma, associated with ISCLS following viral infection. A 74-year-old white male was evaluated in our ocular tumor clinic for a large intraocular mass in the right eye concerning for choroidal melanoma. We completed a review of the literature and list clinical recommendations for these cases. ISCLS, although rare, was a significant diagnostic consideration in this patient. Due to the high mortality rate of this condition, accurate diagnosis and prompt treatment was critical. We hypothesize that the mechanism of choroidal effusion development was due to reduced oncotic pressure from rapid decrease in serum albumin. Increased permeability of choroidal capillaries may be an additional mechanism leading to uveal effusion.

Conclusion: With treatment, the patient had complete resolution of his choroidal effusion with no recurrence of his ISCLS. Further research should be considered on the role of viral infections in the pathogenesis of ISCLS.

Abstract Image

脉络膜积液模拟葡萄膜黑色素瘤:特发性系统性毛细血管渗漏综合征的新表现。
背景:特发性全身毛细血管渗漏综合征(ISCLS,也称为克拉克森病)是一种罕见的医学疾病,其特征是毛细血管内皮细胞功能障碍发作,液体渗漏到间隙,导致严重低血压、血液浓缩、低白蛋白血症和全身性水肿。由于全身灌注不足,每次发作可导致多器官功能衰竭。病例介绍:我们报告一例葡萄膜积液,模拟葡萄膜黑色素瘤,与病毒感染后的ISCLS相关。一位74岁白人男性在我们的眼科肿瘤诊所评估了一个大的眼内肿块在右眼脉络膜黑色素瘤。我们完成了文献回顾,并列出了这些病例的临床建议。ISCLS虽然罕见,但在该患者中是重要的诊断考虑因素。由于这种疾病的高死亡率,准确的诊断和及时的治疗至关重要。我们假设脉络膜积液发生的机制是由于血清白蛋白快速下降导致肿瘤压力降低。脉络膜毛细血管通透性增加可能是导致膜积液的另一个机制。结论:经治疗,患者脉络膜积液完全消失,无复发。病毒感染在ISCLS发病机制中的作用有待进一步研究。
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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来源期刊
CiteScore
2.40
自引率
0.00%
发文量
20
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