Insufficient Diagnostic Value of Serum Galactomannan and (1,3)-β-D-Glucan in Paranasal Sinus Fungus Balls.

Journal of Rhinology Pub Date : 2024-07-01 Epub Date: 2024-07-31 DOI:10.18787/jr.2024.00020
Suk Won Chang, Yeonsu Jeong, Ju Wan Kang, Chang-Hoon Kim, Hyung-Ju Cho
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Abstract

Background and objectives: The serum galactomannan test (GM test) and the (1,3)-β-D-glucan test (G test) are utilized in diagnosing invasive fungal sinusitis. However, their effectiveness in detecting paranasal sinus fungus balls (FBs) has not been established. This study aimed to explore their diagnostic value in patients with FBs.

Methods: We retrospectively reviewed the medical records of 105 patients (42 with FBs and 63 with chronic rhinosinusitis [CRS]) who underwent serum GM and G tests between June 2020 and May 2021. Olfactory test results and demographics were also analyzed.

Results: There were 42 FB patients (10 men, 32 women) and 63 CRS patients (27 men, 36 women). The positivity rates for serum GM (7.1% in the FB group vs. 3.2% in the CRS group, p=0.640) and G test (9.5% in the FB group vs. 11.1% in the CRS group, p=0.482) did not differ significantly between groups. The sensitivities of the GM and G tests were 7.1% and 9.5%, respectively, and their specificities were 96.8% and 88.9%, respectively. The positive predictive values were 60.0% for the GM test and 36.3% for the G test, and the negative predictive values were 61.0% for the GM test and 59.6% for the G test.

Conclusion: Serum GM and G tests demonstrated low sensitivity and high specificity, indicating limited effectiveness in differentiating between patients with FBs and those with CRS. Histological examination remains the gold standard for the definitive diagnosis of FBs.

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血清半乳甘露聚糖和(1,3)-β- d -葡聚糖对副鼻窦真菌球的诊断价值不足。
背景与目的:应用血清半乳甘露聚糖试验(GM试验)和(1,3)-β- d -葡聚糖试验(G试验)诊断侵袭性真菌性鼻窦炎。然而,它们在检测副鼻窦真菌球(FBs)中的有效性尚未确定。本研究旨在探讨其在FBs患者中的诊断价值。方法:我们回顾性分析了2020年6月至2021年5月期间接受血清GM和G检测的105例患者(42例FBs和63例慢性鼻窦炎[CRS])的病历。嗅觉测试结果和人口统计学也进行了分析。结果:FB 42例(男10例,女32例),CRS 63例(男27例,女36例)。血清GM阳性率(FB组为7.1%,CRS组为3.2%,p=0.640)和G检验(FB组为9.5%,CRS组为11.1%,p=0.482)组间差异无统计学意义。GM和G试验的敏感性分别为7.1%和9.5%,特异性分别为96.8%和88.9%。GM检验阳性预测值为60.0%,G检验为36.3%,GM检验阴性预测值为61.0%,G检验阴性预测值为59.6%。结论:血清GM和G检测敏感性低,特异性高,对FBs和CRS的鉴别效果有限。组织学检查仍然是确诊FBs的金标准。
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发文量
23
审稿时长
8 weeks
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