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眼部超声检查:诊断伪装性葡萄膜炎综合征的关键——技巧与窍门

Ocular Ultrasound as a Key to Diagnosing Uveitis-Masked Syndromes: Tips and Tricks.

作者信息

Albano Valeria, Dammacco Rosanna, Lolli Ilaria, Ventricelli Claudia, Settimo Enrico, Miggiano Angelo, Pignataro Maria Grazia, Ferreri Paolo, Boscia Francesco, Guerriero Silvana, Alessio Giovanni

机构信息

Department of Basic Medical Sciences, Neurosciences and Sensory Organs, Eye Clinic, University Hospital Polyclinic of Bari, Piazza Giulio Cesare 11, 70124 Bari, Italy.

Department of Basic Medical Sciences, Neurosciences and Sensory Organs, Eye Clinic, University of Bari, Piazza Giulio Cesare 11, 70124 Bari, Italy.

出版信息

Clin Pract. 2025 Apr 23;15(5):84. doi: 10.3390/clinpract15050084.

DOI:10.3390/clinpract15050084
PMID:40422265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12110100/
Abstract

: Uveitis-masked syndromes or masquerade syndromes (UMSs) are a group of ocular conditions with several systemic underlying causes, malignant or nonmalignant, that mimic the inflammatory status of the uvea. They are often difficult to detect and diagnose with traditional techniques, such as ophthalmic exams. Ocular B (bidimensional)-ultrasound (OBU) is a non-invasive, repeatable, rapid ultrasound method effective in indirect signs that lead back to systemic diseases. It is comparable in effectiveness with other imaging tools. The cause of UMSs can often be serious, and therefore early diagnosis and prompt treatment are critical. This study aimed to identify the sonographic signs of these forms, which can help physicians discover the cause underlying UMS. : This was a consecutive, retrospective, nonrandomized study. This study was conducted at the University Hospital Polyclinic of Bari, Italy, from January 2022 to December 2024. A total of 186 patients were included, from 10 to 85 years old. They all underwent B-scan ultrasonography (Quantel Medical ABSolu Ocular Ultrasound). : All patients reported blurred vision, which could be accompanied by visual reduction (<20/40, Snellen charts), photophobia, floaters, flashes, proptosis, and redness. In all cases, we noted peculiar ultrasonographic signs, which allowed us to discriminate the underlying systemic diagnosis, such as vitreous corpuscles, choroid thickening, and primitive or metastatic solid tumors. Finally, we identified different diseases, such as primary intraocular lymphoma (PIOL), other lymphoproliferative conditions, orbital plasmacytoma, uveal melanoma, metastasis, endogenous endophthalmitis, retinal detachment, central serous retinopathy, metallic foreign bodies, ocular amyloidosis, and drug-induced UMSs. The sensitivity and specificity of ocular ultrasound compared to multimodal ocular imaging in UMSs were as follows: for primary intraocular lymphoma (PIOL) and other lymphoproliferative conditions, 0.98 (95% CI, 0.80-1) and 0.68 (90% CI, 0.40-0.92), respectively; for orbital plasmacytoma, 0.64 (92% CI, 0.52-0.86) and 0.66 (93% CI, 0.48-0.89), respectively; uveal melanoma, 1.00 (98% CI, 0.88-1.00) and 0.98 (95% CI, 0.86-0.98), respectively; metastasis, 0.75 (95% CI, 0.53-0.85) and 0.85 (95% CI, 0.48-0.98), respectively; endogenous endophthalmitis, 1.00 (95% CI, 0.50-1.00) and 0.83 (95% CI, 0.48-0.98), respectively; retinal detachment, both were 1.00 (95% CI, 0.87-1.00 and 0.84-0.97, respectively); central serous retinopathy, 0.60 (80% CI, 0.41-0.88) and 0.85 (95% CI, 0.52-0.98), respectively; metallic foreign bodies, 1.00 (95% CI, 0.78-1.00) and 0.99 (95% CI, 0.99-1.00), respectively; ocular amyloidosis, 0.77 (82% CI, 0.52-0.90) and 0.83 (80% CI, 0.49-0.88), respectively; and drug-induced UMSs, 0.64 (95% CI, 0.49-0.88) and 0.85 (95% CI, 0.52-0.98), respectively. : Diagnosing UMS accurately can be quite challenging, and many of its different types frequently go undetected. This complexity in identification often leads to underdiagnosis, meaning it is essential to improve awareness and understanding of the condition in order to achieve better recognition and treatment. Early detection of these forms is imperative. The use of OBU can help diagnose indirect signs of these forms early and treat them promptly. It compares well with other diagnostic imaging techniques, such as MRI, but this does not mean that it replaces them; it can offer added value in multimodal imaging.

摘要

葡萄膜炎伪装综合征(UMSs)是一组眼部疾病,有多种潜在的全身病因,包括恶性或非恶性病因,这些病因会模仿葡萄膜的炎症状态。它们通常难以用传统技术(如眼科检查)检测和诊断。眼部二维超声(OBU)是一种非侵入性、可重复、快速的超声方法,对提示全身疾病的间接征象有效。其有效性与其他成像工具相当。UMSs的病因往往很严重,因此早期诊断和及时治疗至关重要。本研究旨在识别这些类型的超声征象,这有助于医生发现UMSs的潜在病因。

这是一项连续性、回顾性、非随机研究。该研究于2022年1月至2024年12月在意大利巴里大学医院综合诊所进行。共纳入186例患者,年龄在10至85岁之间。他们均接受了B超检查(Quantel Medical ABSolu眼部超声)。

所有患者均报告有视力模糊,可能伴有视力下降(<20/40,斯内伦视力表)、畏光、飞蚊症、闪光感、眼球突出和眼红。在所有病例中,我们都注意到了特殊的超声征象,这使我们能够鉴别潜在的全身诊断,如玻璃体小体、脉络膜增厚以及原发性或转移性实体瘤。最后,我们识别出了不同的疾病,如原发性眼内淋巴瘤(PIOL)、其他淋巴增殖性疾病、眼眶浆细胞瘤、葡萄膜黑色素瘤、转移瘤、内源性眼内炎、视网膜脱离、中心性浆液性视网膜病变、金属异物、眼部淀粉样变性以及药物性UMSs。与UMSs的多模态眼部成像相比,眼部超声的敏感性和特异性如下:对于原发性眼内淋巴瘤(PIOL)和其他淋巴增殖性疾病,分别为0.98(95%CI,0.80 - 1)和0.68(90%CI,0.40 - 0.92);对于眼眶浆细胞瘤,分别为0.64(92%CI,0.52 - 0.86)和0.66(93%CI,0.48 - 0.89);葡萄膜黑色素瘤,分别为1.00(98%CI,0.88 - 1.00)和0.98(95%CI,0.86 - 0.98);转移瘤,分别为0.75(95%CI,0.53 - 0.85)和0.85(95%CI,0.48 - 0.98);内源性眼内炎,分别为1.00(95%CI,0.50 - 1.00)和0.83(95%CI,0.48 - 0.98);视网膜脱离,两者均为1.00(95%CI,分别为0.87 - 1.00和0.84 - 0.97);中心性浆液性视网膜病变,分别为0.60(80%CI,0.41 - 0.88)和0.85(95%CI,0.52 - 0.98);金属异物,分别为1.00(95%CI,0.78 - 1.00)和0.99(95%CI,0.99 - 1.00);眼部淀粉样变性,分别为0.77(82%CI,0.52 - 0.90)和0.83(80%CI,0.49 - 0.88);以及药物性UMSs,分别为0.64(95%CI,0.49 - 0.88)和0.85(95%CI,0.52 - 0.98)。

准确诊断UMSs可能颇具挑战性,其许多不同类型常常未被发现。这种识别上的复杂性往往导致诊断不足,这意味着提高对该疾病的认识和理解对于实现更好的识别和治疗至关重要。早期发现这些类型势在必行。使用OBU有助于早期诊断这些类型的间接征象并及时进行治疗。它与其他诊断成像技术(如MRI)相比效果良好,但这并不意味着它能取代它们;它可以在多模态成像中提供附加价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a980/12110100/a3fd15c3f0cc/clinpract-15-00084-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a980/12110100/f890332db406/clinpract-15-00084-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a980/12110100/7c7947893e4c/clinpract-15-00084-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a980/12110100/a3fd15c3f0cc/clinpract-15-00084-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a980/12110100/f890332db406/clinpract-15-00084-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a980/12110100/7c7947893e4c/clinpract-15-00084-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a980/12110100/a3fd15c3f0cc/clinpract-15-00084-g003.jpg

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