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Laser-induced fluorescence at 488 nm excitation for detecting benign and malignant lesions in stomach mucosa

机译:激光在488 nm激发下诱导荧光检测胃黏膜的良恶性病变

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摘要

This work aims the detection of the histopathologic alterations of in vitro human gastric mucosa using spectral informations from laser-induced fluorescence spectroscopy (LIFS) technique with excitation at 488 nm (argon laser). A total of 108 biopsies with endoscopic diagnosis of gastritis and gastric cancer were obtained at the antral gastric region, from 35 patients with dyspeptic digestive complaints. The biopsies were collected during the endoscopic examination. On each biopsy fragment the autofluorescence spectrum was collected in two random points, through a fiber-optic catheter coupled to the excitation laser. The fluorescence emission spectra collected by the fibers were directed to the spectrograph and detected by the CCD camera. The spectra were then separated in groups (N, normal; LI, light inflammation; MI, moderated inflammation; CA, adenocarcinoma), based on the histopathology. The ratio between the emission wavelengths 550 and 600 nm was used as a diagnostic parameter. Analysis of fluorescence spectra was able to identify the normal tissue from adenocarcinoma lesions with 100% of sensibility and specificity. The ratio intensities between inflammation (light and moderated), although presented significantly statistical differences when compared to the normal mucosa, do not furnish enough sensibility and specificity for use as an identification method due to high variations. LIFS, with excitation of 488 nm, could be used in the differentiation of normal tissue and neoplasic lesions, assisting a less invasive diagnosis.
机译:这项工作旨在利用在488 nm激发下(氩激光)的激光诱导荧光光谱(LIFS)技术的光谱信息检测体外人胃黏膜的组织病理学改变。从35例消化不良消化不良患者中,在肛门胃区域共进行了108例内镜诊断为胃炎和胃癌的活检。在内窥镜检查期间收集活检。在每个活检片段上,通过耦合到激发激光器的光纤导管在两个随机点收集自发荧光光谱。由纤维收集的荧光发射光谱被引导到光谱仪,并由CCD相机检测。然后根据组织病理学将光谱分为几组(N,正常; LI,轻度炎症; MI,中度炎症; CA,腺癌)。发射波长550和600nm之间的比率被用作诊断参数。荧光光谱分析能够以100%的敏感性和特异性从腺癌病变中识别出正常组织。炎症之间的比率强度(轻度和中度)虽然与正常粘膜相比具有显着的统计学差异,但由于变异大,不能提供足够的敏感性和特异性作为鉴定方法。 LIFS的激发波长为488 nm,可用于正常组织和赘生性病变的分化,从而有助于较低的侵入性诊断。

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