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Diagnosis of cervical squamous intraepithelial lesions by fluorescence imaging: clinical feasibility study

机译:荧光成像诊断宫颈鳞状上皮内病变的临床可行性研究

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OBJECTIVE: Fluorescence diagnosis is still undeveloped in gynaecology. In order to diagnose and localize squamous intraepithelial lesion (SIL) of the cervix, a new method improving the low specificity of colposcopy would be useful. The goal of this study was to assess the feasibility and safety of colposcopic fluorescence diagnosis of SIL after topically application of methyl aminolevulinate (MAL). PATIENTS AND METHODS: Patients with histologic proved cervical intraepithelial neoplasia (CIN) and planned for loop electrosurgical excision procedure (LEEP) under general anesthesia were included in a prospective study. Before general anesthesia, a thick layer of MAL (Metvix-160 mg/mL cream) was applied on the cervix for 35-150 min. Fluorescent colposcopic inspection of the cervix was performed using a rigid 10-mm laparoscope inserted in the vaginal cavity and connected to D-light AF system (Karl Storz Endoskope, Tuttlingen Germany). In order to confirm neoplasic status, fluorescent foci underwent directed punch biopsy(ies). RESULTS: Fourteen patients were included in the study. Colposcopic fluorescence imaging revealed red fluorescent foci in 71.4% of cases (10/14) (neoplasic status of fluorescent foci was confirmed in 80%). Concerning MAL, the mean of application time was 73 min (35-150). Two cases presented a false-positive fluorescence and four cases of false-negative fluorescence. For all cases of false-negative fluorescence, application time of MAL was less than 60 min. We observed no systemic or local toxicity of MAL application in any group. DISCUSSION AND CONCLUSION: Using topical application of MAL to the cervix, we demonstrated that fluorescence diagnosis of SIL is feasible. This study justifies the further development of fluorescence imaging that combines classical white light colposcopy with the use of a photosensitizer.
机译:目的:荧光诊断在妇科中尚不成熟。为了诊断和定位宫颈鳞状上皮内病变(SIL),一种改善阴道镜检查低特异性的新方法将是有用的。这项研究的目的是评估局部应用氨基乙酰丙酸甲酯(MAL)的阴道镜荧光诊断SIL的可行性和安全性。患者与方法:前瞻性研究包括经组织学证实为宫颈上皮内瘤样变(CIN)并计划在全身麻醉下进行环行电外科切除术(LEEP)的患者。在全身麻醉之前,将一层厚厚的MAL(Metvix-160 mg / mL乳膏)涂在子宫颈上35-150分钟。使用插入阴道腔并连接至D-light AF系统(Karl Storz Endoskope,德国图特林根)的10毫米刚性腹腔镜对子宫颈进行荧光阴道镜检查。为了确认赘生物的状态,对荧光灶进行了定向打孔活检。结果:14名患者被纳入研究。阴道镜下的荧光成像显示71.4%的病例为红色荧光灶(10/14)(已确认80%的病例为荧光灶的肿瘤状态)。关于MAL,平均应用时间为73分钟(35-150)。 2例呈假阳性荧光,4例呈假阴性荧光。对于所有假阴性荧光的情况,MAL的应用时间少于60分钟。我们观察到在任何组中,MAL施用均无全身或局部毒性。讨论与结论:通过对宫颈局部应用MAL,我们证明了SIL的荧光诊断是可行的。这项研究证明了将经典的白光阴道镜与光敏剂结合使用的荧光成像技术的进一步发展是合理的。

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