在临床评估和皮肤镜检查之外,利用电阻抗能谱数据可显著改善对色素性皮肤病进行活检的决定

D. Zakria, Nicholas Brownstone, Klaus Fritz, Carmen Salavastru, Darrell S Rigel
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引用次数: 0

摘要

背景:即使是最有经验的皮肤科医生也可能会放弃对多达三分之一的恶性黑色素瘤(MM)进行活组织检查。电阻抗光谱(EIS)是一种无创技术,它能通过色素病变发出无痛、电压极低的电流,以确定病变是良性还是恶性。本研究旨在确定 EIS 数据是否能改善对色素性病变进行活检的决定,甚至超过皮肤镜检查。研究方法在一次全国性会议上向皮肤科医生展示了一份调查表,其中包含 49 幅 MMs、严重发育不良痣 (SDN) 和良性色素性皮肤病变 (PSL) 的图像。他们被问及在第一次看到临床图像后是否会对病变进行活组织检查,在看到皮肤镜图像后是否会再次进行活组织检查,在得到 EIS 评分后是否会再次进行活组织检查。结果:151 名皮肤科医生完成了调查。对于 MM(78.5% 对 56.2%,P<0.01)和 SDN(62.7% 对 43.8%,P<0.01),受访者做出正确活检决定(对 MM 和 SDN 进行活检,并放弃对良性 PSL 进行活检)的比例明显高于仅使用临床图像的比例。对于 MM(86.2% vs. 78.9%,p<0.01)、SDN(68.1% vs. 62.7%,p<0.05)和良性病变(58.7% vs. 48.0% vs,p<0.01),在整合 EIS 评分后,参与者在皮肤镜评估之外做出正确活检决定的比例也有统计学意义的显著提高。结论EIS 能够进一步提高 MM 和 SDN 活检选择的正确率,甚至超过皮肤镜评估。虽然皮肤镜检查会降低良性 PSL 的诊断准确性,但 EIS 的结果也能显著改善这些病变的决策。这项研究证明了 EIS 技术在改善黑色素瘤诊断方面的临床实用性。
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Utilizing Data from Electrical Impedance Spectroscopy Significantly Improves the Decision to Biopsy Pigmented Skin Lesions Beyond Clinical Evaluation and Dermoscopy
Background: Even the most experienced dermatologists may forego a biopsy on as many as one-third of malignant melanomas (MMs). Electrical impedance spectroscopy (EIS) is a noninvasive technology that send a painless, very low voltage electrical current through a pigmented lesion to determine if it is benign or malignant. This study aimed to determine if EIS data can improve the decision to biopsy a pigmented lesion even beyond dermoscopy. Methods: A survey with 49 images of MMs, severe dysplastic nevi (SDNs), and benign pigmented skin lesions (PSLs) was shown to dermatologists at a national conference. They were asked if they would biopsy the lesion after first seeing the clinical image, then again after seeing the dermoscopic image, and again after receiving the EIS score. Results: 151 dermatologists completed the survey. Respondents significantly increased correct biopsy decisions (biopsy MMs and SDNs and forego biopsy of benign PSLs) with the addition of dermoscopy versus clinical image alone for MM (78.5% vs. 56.2%, p<0.01) and SDN (62.7% vs. 43.8%, p<0.01). Participants also demonstrated a statistically significant increase in correct biopsy decisions beyond the dermoscopic evaluation when integrating the EIS score for MM (86.2% vs. 78.9%, p<0.01), SDN (68.1% vs. 62.7%, p<0.05) and benign lesions (58.7% vs. 48.0% vs, p<0.01). Conclusion: EIS was able to further improve the rate of correct biopsy choice for MMs and SDNs even beyond dermoscopic evaluation. While dermoscopy worsened diagnostic accuracy for benign PSLs, EIS results were able to significantly improve decision making for these lesions as well. This study demonstrates the clinical utility of EIS technology for improving melanoma diagnosis.
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