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Quality Assessment of Endoscopic Forceps Biopsy Samples under Magnifying Narrow Band Imaging for Histological Diagnosis of Cervical Intraepithelial Neoplasia: A Feasibility Study

机译:放大窄带成像下内镜钳活组织检查样本的质量评估用于宫颈上皮内瘤的组织学诊断:可行性研究

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摘要

The current standard for diagnosing cervical intraepithelial neoplasia (CIN) is colposcopy followed by punch biopsy. We have developed flexible magnifying endoscopy with narrow band imaging (ME-NBI) for the diagnosis of CIN. Here, we investigated the feasibility of targeted endoscopic forceps biopsy (E-Bx) under guidance of ME-NBI for the diagnosis of CIN. We prospectively enrolled 32 consecutive patients with confirmed or suspected high-grade CIN undergoing cervical conization. Next to colposcopy, the same patients underwent ME-NBI just before conization. ME-NBI was performed, and 30 E-Bx samples were taken from lesions suspicious for high-grade CIN and 15 from non-suspicious mucosa. We recalled 82 punch biopsy (P-Bx) specimens taken from lesions suspicious for high-grade CIN under colposcopic examination before enrollment. The proportion of sufficient biopsy samples, which had an entire mucosal layer with subepithelial tissue, for the diagnosis of CIN was evaluated by both methods. Performance of targeted E-Bx for the final diagnosis of at least high-grade CIN was calculated. Seventeen P-Bx specimens were unavailable. The proportion of sufficient samples with E-Bx was 84%, which was similar to that with P-Bx (87%) (p = 0.672). The sensitivity, specificity, and accuracy of ME-NBI using E-Bx was 92%, 81%, and 88%, respectively. In conclusion, ME-NBI-guided E-Bx samples were feasible for histological diagnoses of CIN, and further investigation of its diagnostic accuracy is warranted.
机译:诊断宫颈上皮内瘤周期(CIN)的目前的标准是阴镜检查,然后进行冲头活检。我们开发了灵活的放大镜内窥镜,具有窄带成像(ME-NBI),用于诊断CIN。在这里,我们研究了在ME-NBI的指导下针对靶向内镜钳活组织检查(E-BX)的可行性进行诊断。我们预期32例连续32例患有宫颈癌的确诊或疑似高等CIN。在阴道镜检查旁边,同一患者在截然之前接受了ME-NBI。进行ME-NBI,并从损伤中取出30 e-BX样品,用于高等CIN和15来自非可疑粘膜。我们回忆起82个穿孔活检(P-BX)标本,在入学前在阴道镜检查下对高级CIN的病灶可疑。通过两种方法评估具有具有耻骨皮肤组织的全部粘膜层的足够活组织检查样品的比例,用于通过两种方法评估CIN的诊断。计算靶向E-BX的最终诊断的性能,但至少高级CIN的最终诊断。 17个P-BX样本不可用。用E-Bx充分样品的比例为84%,与P-Bx(87%)相似(P = 0.672)。 ME-NBI使用E-BX的敏感性,特异性和准确性分别为92%,81%和88%。总之,ME-NBI引导的E-BX样品对于CIN的组织学诊断是可行的,并且有权进一步调查其诊断准确性。

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