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In Vivo Imaging Techniques for the Human Scalp: A Systematic Review of the Literature 人体头皮活体成像技术:文献系统回顾。
IF 2.2 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-26 DOI: 10.1002/lsm.23835
Bobak Hedayati, Luke Horton, Brittany Urso, Chloe Ekelem, Arash Babadjouni, Ajay N. Sharma, Natasha Atanaskova Mesinkovska

Objective

Scalp inflammation and alopecia are distressing conditions for which patients regularly present to dermatology. Although some diagnoses can be made clinically, others require biopsy, which carries the risk of pain, infection, bleeding, and scarring. This review examines the existing literature regarding noninvasive in vivo imaging techniques and their evidence and utility in evaluating scalp pathology, with a focus on the diagnostics of hair conditions.

Methods

A systematic literature search was conducted using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines without timeframe restrictions. The PubMed and Clarivate (Web of Science) databases were searched using the terms (“imaging” OR “in-vivo imaging” OR “non-invasive imaging” OR “non-invasive in vivo imaging” “imaging,” “in-vivo imaging) AND (“human scalp disorders” OR “scalp” OR “hair loss” OR “alopecia”). Peer-reviewed randomized control trials (RCTs), prospective studies, retrospective studies, and case series or reports discussing in vivo imaging of the scalp published before 2022 were selected.

Results

Forty-two studies were included and discussed; modalities included laser devices (n = 27), ultrasound (US) (n = 13), infrared thermography (n = 1), skin capacitance imaging (SCI), and ultraviolet light–enhanced visualization (ULEV) (n = 1). The most common laser devices used were reflectance confocal microscopy (RCM), multiphoton microscopy (MPM), and optical coherence tomography (OCT). US techniques included high-frequency US (HFUS) and US biomicroscopy (UBM).

Conclusion

Quality imaging of the scalp in the setting of alopecic, neoplastic, and inflammatory diseases is highly sought after. Many of these noninvasive imaging techniques show promise, each with individual advantages and disadvantages in imaging-specific conditions. Ultimately, noninvasive imaging techniques may be used to optimize patient management and minimize morbidity associated with scalp biopsies.

目的:头皮发炎和脱发是一种令人苦恼的疾病,患者经常因此到皮肤科就诊。虽然有些诊断可以通过临床方式做出,但有些则需要进行活检,而活检会带来疼痛、感染、出血和疤痕的风险。本综述研究了有关无创活体成像技术及其在评估头皮病理方面的证据和效用的现有文献,重点是毛发病症的诊断:采用《系统综述和元分析首选报告项目》(PRISMA)指南进行了系统性文献检索,没有时间限制。使用术语("成像 "或 "体内成像 "或 "无创成像 "或 "无创体内成像""成像""体内成像")和("人类头皮疾病 "或 "头皮 "或 "脱发 "或 "脱发症")在 PubMed 和 Clarivate(Web of Science)数据库中进行检索。选择了同行评议的随机对照试验(RCT)、前瞻性研究、回顾性研究以及 2022 年之前发表的讨论头皮活体成像的系列病例或报告:共纳入并讨论了 42 项研究;研究方式包括激光设备(n = 27)、超声波(US)(n = 13)、红外热成像(n = 1)、皮肤电容成像(SCI)和紫外线增强可视化(ULEV)(n = 1)。最常用的激光设备是反射共聚焦显微镜(RCM)、多光子显微镜(MPM)和光学相干断层扫描(OCT)。US 技术包括高频 US(HFUS)和 US 生物显微镜(UBM):结论:脱发、肿瘤和炎症性疾病患者对头皮成像的质量要求很高。许多无创成像技术都显示出了良好的前景,但在成像特定病症时各有利弊。最终,无创成像技术可用于优化患者管理,最大限度地降低头皮活检的发病率。
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引用次数: 0
Timing of Laser Intervention on Facial Scars: A 3D Imaging and Scar Scale Analysis in a Retrospective Study 激光干预面部疤痕的时机:一项回顾性研究中的三维成像和疤痕尺度分析
IF 2.2 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-22 DOI: 10.1002/lsm.23846
Shuai Qiang, Xing Fan, Yue Yin, Ping Xue, Wen-Jie Dou, Tong Li, Qing Yang
<div> <section> <h3> Objectives</h3> <p>Scars resulting from injuries or surgical procedures often present both physical and aesthetic challenges. Recent studies have indicated promising results in improving postoperative scar outcomes through the combined use of specific laser technologies. Nevertheless, there remains a crucial need for further exploration to ascertain the optimal timing for initiating such treatments.</p> </section> <section> <h3> Methods</h3> <p>In this retrospective investigation, a cohort of 47 adult patients who did not require hospitalization was analyzed. These patients were divided into two distinct groups: Group A, which received intervention beginning 2 weeks after their respective operations, and Group B, which commenced intervention 4 weeks postoperation. Each group underwent a comprehensive treatment protocol consisting of five laser sessions. Initially, patients underwent three sessions of V-beam pulsed-dye laser (PDL) therapy followed by two sessions of ablative fractional CO<sub>2</sub> laser (AFL) therapy. Evaluation of outcomes was conducted using advanced imaging techniques such as Antera 3D imaging, in conjunction with established scar assessment tools including the Vancouver Scar Scale (VSS) and the University of North Carolina “4P” Scar Scale (UNC4P).</p> </section> <section> <h3> Results</h3> <p>All patients successfully completed the full course of five treatment sessions, with no dropouts and no reported adverse events. Baseline cosmetic assessments of scars were equivalent across both groups. In Group A, the mean VSS scores decreased from 7.04 before treatment to 5.29 at 3 months posttreatment and further to 4.33 at 6 months posttreatment. Meanwhile, in Group B, scores decreased from 7.52 to 6.83 at 3 months and 6.17 at 6 months. There were no statistically significant differences in baseline VSS scores between the two groups (<i>p</i> = 0.34). At both the 3- and 6-month follow-up points, mean VSS scores were significantly lower in Group A compared to Group B (<i>p</i> < 0.05). Similar trends were observed in UNC4P scores. Statistically significant differences were noted across all time points (baseline, 3 months, and 6 months posttreatment) for both VSS and UNC4P scores (<i>p</i> < 0.05). Subset analysis revealed greater improvements in texture and depression volume at 3 months posttreatment, while improvements in depression area, depth, elevation variation, and area were more pronounced at the 6-month mark.</p> </section> <section> <h3> Conclusions</h3> <p>Early intervention using the combined 595-nm pulse dye laser and CO<sub>2</sub> ablative fractional laser (AFL) 2- and 4-week
目的:受伤或手术后留下的疤痕通常会给身体和美观带来双重挑战。最近的研究表明,通过联合使用特定的激光技术,在改善术后疤痕效果方面取得了可喜的成果。尽管如此,我们仍需进一步探索,以确定启动此类治疗的最佳时机:在这项回顾性调查中,我们对 47 名无需住院治疗的成年患者进行了分析。这些患者被分为两组:A 组在各自手术后 2 周开始接受干预,B 组在手术后 4 周开始干预。每组患者都接受了由五个激光疗程组成的综合治疗方案。首先,患者接受三个疗程的V型束脉冲染料激光(PDL)治疗,然后接受两个疗程的烧蚀点阵二氧化碳激光(AFL)治疗。疗效评估采用先进的成像技术,如 Antera 3D 成像技术,并结合成熟的疤痕评估工具,包括温哥华疤痕量表(VSS)和北卡罗来纳大学 "4P "疤痕量表(UNC4P):结果:所有患者都顺利完成了五个疗程的治疗,无一中途退出,也无不良反应报告。两组患者的疤痕基线美容评估结果相同。A 组患者的平均 VSS 分数从治疗前的 7.04 分降至治疗后 3 个月的 5.29 分,再降至治疗后 6 个月的 4.33 分。与此同时,B 组的评分从治疗前的 7.52 分降至治疗后 3 个月时的 6.83 分和治疗后 6 个月时的 6.17 分。两组的 VSS 基线得分在统计学上没有明显差异(P = 0.34)。在 3 个月和 6 个月的随访中,A 组的 VSS 平均得分均明显低于 B 组(p 结论:B 组的 VSS 平均得分明显低于 A 组):手术后 2 周和 4 周使用 595 纳米脉冲染料激光和二氧化碳烧蚀点阵激光(AFL)联合疗法进行早期干预,证明是一种有效且安全的改善疤痕效果的方法,尤其是在手术后 2 周开始治疗面部手术疤痕时。然而,我们还需要进一步的研究来完善我们的认识并解决潜在的研究局限性。
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引用次数: 0
Use of Optical Coherence Tomography to Assess Properties of Cutaneous Defects Following Radiofrequency Microneedling and Laser Treatment 使用光学相干断层扫描评估射频微针和激光治疗后皮肤缺陷的特性。
IF 2.2 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-22 DOI: 10.1002/lsm.23840
Kira Seiger, William Driscoll, Feben Messele, Nicole M. Golbari, Xiying Fan, Jon Holmes, Christopher B. Zachary

Objectives

To characterize the properties of cutaneous defects created by energy-based devices using optical coherence tomography.

Materials and Methods

Radiofrequency (RF) microneedling and non-ablative fractional laser (NAFL) treatment were performed in vivo with various parameters. Following treatment, optical coherence tomography (OCT) was used to image and measure cutaneous defects at multiple time points over a 24 h period.

Results

Channel-like cutaneous defects were visible with OCT following bipolar RF microneedling and NAFL treatment. Using a double pulse technique with RF microneedling yielded a greater number of defects visible with OCT, as well as defects that were deeper and more durable over time. Following treatment with 1927 nm thulium fiber laser, the average diameter of the defects was greater when the energy level was 20 mJ as compared to 10 mJ (0.33 mm vs. 0.27 mm, p < 0.01).

Conclusions

Cutaneous defects were observed following both RF microneedling and NAFL treatment. Properties of the cutaneous defects varied based on device, treatment setting, and technique, which may be useful in guiding further study of device-assisted drug delivery.

目的利用光学相干断层扫描技术描述能量设备造成的皮肤缺陷的特性:采用不同参数在体内进行射频(RF)微针和非烧蚀点阵激光(NAFL)治疗。治疗后,使用光学相干断层扫描(OCT)对 24 小时内多个时间点的皮肤缺陷进行成像和测量:结果:双极射频微针和 NAFL 治疗后,光学相干断层扫描(OCT)显示出通道状皮肤缺损。使用射频微针的双脉冲技术可产生更多的 OCT 可见缺损,而且缺损更深,随着时间的推移更持久。使用 1927 nm 铥光纤激光治疗后,能量水平为 20 mJ 时,缺陷的平均直径大于 10 mJ(0.33 毫米对 0.27 毫米,p 结论):射频微针和 NAFL 治疗后都会出现皮肤缺损。皮肤缺损的性质因设备、治疗设置和技术而异,这可能有助于指导对设备辅助给药的进一步研究。
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引用次数: 0
Defining the Treatment Window: Early Versus Late Pulsed Dye Laser Therapy for Posttraumatic and Surgical Scars in Asian Patients. 确定治疗窗口:亚洲患者创伤后和手术后疤痕的早期脉冲染料激光疗法与晚期脉冲染料激光疗法。
IF 2.2 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-22 DOI: 10.1002/lsm.23844
Han-Yuan Chang, Bing-Qi Wu, Chang-Cheng Chang, Yu-Tsung Chen, Yen-Jen Wang

Objectives: This retrospective study evaluates the effectiveness of pulsed dye laser (PDL) treatment in early versus late treatment groups for traumatic or postoperative scars. The study aims to determine the threshold between early and late treatment. Additionally, it investigates factors that may influence wound healing outcomes.

Methods: The medical records of 147 patients who underwent PDL treatment at our institution between January 2018 and December 2022 were retrospectively reviewed. Inclusion criteria were patients receiving PDL treatment for traumatic or postoperative scars. Out of these patients, we selected those who were willing to receive telephone interviews or re-visit at a scheduled time. Eventually, 52 participants were included in our study. A standardized questionnaire was administered to all participants during telephone interviews, encompassing inquiries regarding their medical history, treatment experiences, and the patient component of the Patient and Observer Scar Assessment Scale. Among the enrolled patients, 38 were contacted and interviewed via telephone, while the remaining 14 patients attended follow-up visits where photographs of their current skin condition were captured. The pretreatment and latest follow-up photographs obtained from the clinical database were independently scored in a blinded manner by two dermatologist reviewers using both the Vancouver Scar Scale and the Manchester Scar Scale.

Results: Among the 52 patients, 43 (82.7%) were successfully treated with good response. The correlation coefficients between week-to-treatment initiation and posttreatment MSS and VSS among patients with good response were 0.50 (p < 0.001) and 0.46 (p = 0.002), respectively. Given these findings, we established a treatment initiation threshold of 10 weeks, distinguishing patients into early and late treatment groups. The early treatment group showed borderline significantly lower posttreatment MSS and VSS scores than the late treatment group (MSS: 7.5 ± 2.1 vs. 9.3 ± 2.5, p = 0.011; VSS: 2.8 ± 2.0 vs. 4.5 ± 2.3, p = 0.011). Furthermore, both MSS and VSS of posttreatment showed significantly greater improvement in the early treatment group (4.4 ± 1.6 vs. 3.2 ± 1.9; p = 0.03 and 3.8 ± 1.8 vs. 2.8 ± 1.4; p = 0.04).

Conclusions: Early intervention using a PDL within 10 weeks post-injury achieved better outcomes in treating traumatic and postoperative scars based on both clinical and patient opinions.

研究目的这项回顾性研究评估了脉冲染料激光(PDL)治疗创伤性或术后疤痕的早期治疗组和晚期治疗组的疗效。研究旨在确定早期治疗和晚期治疗之间的临界值。此外,该研究还调查了可能影响伤口愈合结果的因素:回顾性审查了 2018 年 1 月至 2022 年 12 月期间在我院接受 PDL 治疗的 147 名患者的病历。纳入标准为因外伤或术后疤痕而接受 PDL 治疗的患者。在这些患者中,我们选择了愿意接受电话访谈或在预定时间再次就诊的患者。最终,52 名参与者被纳入了我们的研究。在电话访谈中,我们向所有参与者发放了一份标准化问卷,内容包括询问他们的病史、治疗经历以及患者和观察者疤痕评估量表中的患者部分。在登记的患者中,有 38 人接受了电话联系和访谈,其余 14 人接受了随访,并拍摄了当前皮肤状况的照片。从临床数据库中获得的治疗前照片和最近的随访照片由两名皮肤科医生使用温哥华疤痕量表和曼彻斯特疤痕量表进行盲法独立评分:52 名患者中,43 人(82.7%)治疗成功,反应良好。在反应良好的患者中,治疗开始一周与治疗后 MSS 和 VSS 之间的相关系数为 0.50(p 结论:PDL 是治疗疤痕的最佳方法:根据临床和患者的意见,在受伤后 10 周内使用 PDL 进行早期干预,在治疗外伤和术后疤痕方面取得了更好的效果。
{"title":"Defining the Treatment Window: Early Versus Late Pulsed Dye Laser Therapy for Posttraumatic and Surgical Scars in Asian Patients.","authors":"Han-Yuan Chang, Bing-Qi Wu, Chang-Cheng Chang, Yu-Tsung Chen, Yen-Jen Wang","doi":"10.1002/lsm.23844","DOIUrl":"https://doi.org/10.1002/lsm.23844","url":null,"abstract":"<p><strong>Objectives: </strong>This retrospective study evaluates the effectiveness of pulsed dye laser (PDL) treatment in early versus late treatment groups for traumatic or postoperative scars. The study aims to determine the threshold between early and late treatment. Additionally, it investigates factors that may influence wound healing outcomes.</p><p><strong>Methods: </strong>The medical records of 147 patients who underwent PDL treatment at our institution between January 2018 and December 2022 were retrospectively reviewed. Inclusion criteria were patients receiving PDL treatment for traumatic or postoperative scars. Out of these patients, we selected those who were willing to receive telephone interviews or re-visit at a scheduled time. Eventually, 52 participants were included in our study. A standardized questionnaire was administered to all participants during telephone interviews, encompassing inquiries regarding their medical history, treatment experiences, and the patient component of the Patient and Observer Scar Assessment Scale. Among the enrolled patients, 38 were contacted and interviewed via telephone, while the remaining 14 patients attended follow-up visits where photographs of their current skin condition were captured. The pretreatment and latest follow-up photographs obtained from the clinical database were independently scored in a blinded manner by two dermatologist reviewers using both the Vancouver Scar Scale and the Manchester Scar Scale.</p><p><strong>Results: </strong>Among the 52 patients, 43 (82.7%) were successfully treated with good response. The correlation coefficients between week-to-treatment initiation and posttreatment MSS and VSS among patients with good response were 0.50 (p < 0.001) and 0.46 (p = 0.002), respectively. Given these findings, we established a treatment initiation threshold of 10 weeks, distinguishing patients into early and late treatment groups. The early treatment group showed borderline significantly lower posttreatment MSS and VSS scores than the late treatment group (MSS: 7.5 ± 2.1 vs. 9.3 ± 2.5, p = 0.011; VSS: 2.8 ± 2.0 vs. 4.5 ± 2.3, p = 0.011). Furthermore, both MSS and VSS of posttreatment showed significantly greater improvement in the early treatment group (4.4 ± 1.6 vs. 3.2 ± 1.9; p = 0.03 and 3.8 ± 1.8 vs. 2.8 ± 1.4; p = 0.04).</p><p><strong>Conclusions: </strong>Early intervention using a PDL within 10 weeks post-injury achieved better outcomes in treating traumatic and postoperative scars based on both clinical and patient opinions.</p>","PeriodicalId":17961,"journal":{"name":"Lasers in Surgery and Medicine","volume":" ","pages":""},"PeriodicalIF":2.2,"publicationDate":"2024-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142290319","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The 2910-nm Fiber Laser Is Safe and Effective for Improving Acne Scarring 2910 波长光纤激光器可安全有效地改善痤疮疤痕。
IF 2.2 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-22 DOI: 10.1002/lsm.23845
Eric Bernstein, Ali Alajmi, Jennifer Wang, Edward Hochman, Brian Biesman, James F. Sanzo

Background

Acne scarring results from the inflammation associated with acne papules, which alters dermal collagen, typically producing depressed scars. Lasers have been used to remodel skin improving the texture and appearance of acne scars. Herein, we investigate a new 2910 nm, erbium-doped, fluoride glass, fiber laser for improving acne scars. This novel laser delivers up to 5000 Hz low-energy pulses, providing a unique treatment modality.

Methods

Fourteen subjects with rolling and/or boxcar acne scars were enrolled in this study. Thirteen subjects completed the final visit and received three treatments with the 2910 nm fiber laser at 6–8-week intervals. Eight subjects were Fitzpatrick type II and five were Fitzpatrick type III. Digital images were taken pre- and 1- and 3-months posttreatment and evaluated by two blinded reviewers in a randomized fashion for improvement. Subjects and the treating physician completed a Global Aesthetic Improvement Scale (GAIS) before treatment and at each visit to subjectively evaluate treatment effect. Histological analysis was performed on ex vivo lower eyelid skin samples. Side effects were evaluated by the treating physician and included erythema, edema, and pinpoint bleeding.

Results

Evaluation of blinded digital images revealed a mean improvement of 47.3% ± 14.2% (mean ± SEM) 3 months following the final treatment. GAIS scores demonstrated improvement as evaluated by both the subjects and the treating physician. Side effects averaged trace-to-mild erythema, edema, and pinpoint bleeding.

Conclusion

This study shows that the 2910 nm, erbium-doped, fluoride glass, fiber laser is safe and effective for improving the appearance of acne scars.

背景:痤疮疤痕是由于痤疮丘疹引起的炎症改变了真皮胶原蛋白,通常会产生凹陷性疤痕。激光已被用于重塑皮肤,改善痤疮疤痕的质地和外观。在此,我们研究了一种用于改善痤疮疤痕的新型 2910 纳米掺铒氟化玻璃光纤激光器。这种新型激光可发出高达 5000 Hz 的低能量脉冲,提供了一种独特的治疗方式:本研究共招募了 14 名患有滚动式和/或箱形痤疮疤痕的受试者。13名受试者完成了最后一次检查,并在6-8周的间隔时间内接受了三次2910纳米光纤激光治疗。八名受试者为 Fitzpatrick II 型,五名为 Fitzpatrick III 型。治疗前、治疗后 1 个月和 3 个月拍摄数码图像,并由两名盲人评审员以随机方式对改善情况进行评估。受试者和主治医师在治疗前和每次就诊时都填写了全球美学改善量表(GAIS),以主观评估治疗效果。对活体下眼睑皮肤样本进行组织学分析。副作用由主治医生评估,包括红斑、水肿和针尖出血:结果:盲法数字图像评估显示,最终治疗 3 个月后,平均改善率为 47.3% ± 14.2%(平均值 ± SEM)。根据受试者和主治医生的评估,GAIS 评分均有所改善。副作用平均为微量至轻度红斑、水肿和针尖出血:这项研究表明,2910 纳米掺铒氟化玻璃光纤激光器对改善痤疮疤痕外观安全有效。
{"title":"The 2910-nm Fiber Laser Is Safe and Effective for Improving Acne Scarring","authors":"Eric Bernstein,&nbsp;Ali Alajmi,&nbsp;Jennifer Wang,&nbsp;Edward Hochman,&nbsp;Brian Biesman,&nbsp;James F. Sanzo","doi":"10.1002/lsm.23845","DOIUrl":"10.1002/lsm.23845","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Acne scarring results from the inflammation associated with acne papules, which alters dermal collagen, typically producing depressed scars. Lasers have been used to remodel skin improving the texture and appearance of acne scars. Herein, we investigate a new 2910 nm, erbium-doped, fluoride glass, fiber laser for improving acne scars. This novel laser delivers up to 5000 Hz low-energy pulses, providing a unique treatment modality.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>Fourteen subjects with rolling and/or boxcar acne scars were enrolled in this study. Thirteen subjects completed the final visit and received three treatments with the 2910 nm fiber laser at 6–8-week intervals. Eight subjects were Fitzpatrick type II and five were Fitzpatrick type III. Digital images were taken pre- and 1- and 3-months posttreatment and evaluated by two blinded reviewers in a randomized fashion for improvement. Subjects and the treating physician completed a Global Aesthetic Improvement Scale (GAIS) before treatment and at each visit to subjectively evaluate treatment effect. Histological analysis was performed on ex vivo lower eyelid skin samples. Side effects were evaluated by the treating physician and included erythema, edema, and pinpoint bleeding.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Evaluation of blinded digital images revealed a mean improvement of 47.3% ± 14.2% (mean ± SEM) 3 months following the final treatment. GAIS scores demonstrated improvement as evaluated by both the subjects and the treating physician. Side effects averaged trace-to-mild erythema, edema, and pinpoint bleeding.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>This study shows that the 2910 nm, erbium-doped, fluoride glass, fiber laser is safe and effective for improving the appearance of acne scars.</p>\u0000 </section>\u0000 </div>","PeriodicalId":17961,"journal":{"name":"Lasers in Surgery and Medicine","volume":"56 9","pages":"755-761"},"PeriodicalIF":2.2,"publicationDate":"2024-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lsm.23845","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142290323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Physician Level Assessment of Hirsute Women and of Their Eligibility for Laser Treatment With Deep Learning. 利用深度学习对多毛女性及其接受激光治疗的资格进行医生级别的评估。
IF 2.2 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-22 DOI: 10.1002/lsm.23843
Kenneth Thomsen, Raluca Jalaboi, Ole Winther, Hans Bredsted Lomholt, Henrik F Lorentzen, Trine Høgsberg, Henrik Egekvist, Lene Hedelund, Sofie Jørgensen, Sanne Frost, Trine Bertelsen, Lars Iversen

Objectives: Hirsutism is a widespread condition affecting 5%-15% of females. Laser treatment of hirsutism has the best long-term effect. Patients with nonpigmented or nonterminal hairs are not eligible for laser treatment, and the current patient journey needed to establish eligibility for laser hair removal is problematic in many health-care systems.

Methods: In this study, we compared the ability to assess eligibility for laser hair removal of health-care professionals and convolutional neural network (CNN)-based models.

Results: The CNN ensemble model, synthesized from the outputs of five individual CNN models, reached an eligibility assessment accuracy of 0.52 (95% CI: 0.42-0.60) and a κ of 0.20 (95% CI: 0.13-0.27), taking a consensus expert label as reference. For comparison, board-certified dermatologists achieved a mean accuracy of 0.48 (95% CI: 0.44-0.52) and a mean κ of 0.26 (95% CI: 0.22-0.31). Intra-rater analysis of board-certified dermatologists yielded κ in the 0.32 (95% CI: 0.24-0.40) and 0.65 (95% CI: 0.56-0.74) range.

Conclusion: Current assessment of eligibility for laser hair removal is challenging. Developing a laser hair removal eligibility assessment tool based on deep learning that performs on a par with trained dermatologists is feasible. Such a model may potentially reduce workload, increase quality and effectiveness, and facilitate equal health-care access. However, to achieve true clinical generalizability, prospective randomized clinical intervention studies are needed.

目的:多毛症是一种常见病,影响 5%-15%的女性。激光治疗多毛症的长期效果最佳。非色素性毛发或非末端毛发患者不符合激光治疗的条件,而目前许多医疗保健系统在确定激光脱毛资格所需的患者旅程方面存在问题:在这项研究中,我们比较了医疗保健专业人员和基于卷积神经网络(CNN)模型的激光脱毛资格评估能力:结果:由五个单独的 CNN 模型输出合成的 CNN 组合模型,以专家共识标签为参考,合格评估准确率达到 0.52(95% CI:0.42-0.60),κ为 0.20(95% CI:0.13-0.27)。相比之下,获得资格认证的皮肤科医生的平均准确率为 0.48(95% CI:0.44-0.52),平均κ为 0.26(95% CI:0.22-0.31)。对获得认证的皮肤科医生进行的内部评分分析得出的κ范围分别为0.32(95% CI:0.24-0.40)和0.65(95% CI:0.56-0.74):结论:目前对激光脱毛资格的评估具有挑战性。开发一种基于深度学习的激光脱毛资格评估工具是可行的,其性能可与训练有素的皮肤科医生媲美。这种模型有可能减少工作量、提高质量和有效性,并促进平等的医疗服务。不过,要实现真正的临床普及,还需要进行前瞻性随机临床干预研究。
{"title":"Physician Level Assessment of Hirsute Women and of Their Eligibility for Laser Treatment With Deep Learning.","authors":"Kenneth Thomsen, Raluca Jalaboi, Ole Winther, Hans Bredsted Lomholt, Henrik F Lorentzen, Trine Høgsberg, Henrik Egekvist, Lene Hedelund, Sofie Jørgensen, Sanne Frost, Trine Bertelsen, Lars Iversen","doi":"10.1002/lsm.23843","DOIUrl":"https://doi.org/10.1002/lsm.23843","url":null,"abstract":"<p><strong>Objectives: </strong>Hirsutism is a widespread condition affecting 5%-15% of females. Laser treatment of hirsutism has the best long-term effect. Patients with nonpigmented or nonterminal hairs are not eligible for laser treatment, and the current patient journey needed to establish eligibility for laser hair removal is problematic in many health-care systems.</p><p><strong>Methods: </strong>In this study, we compared the ability to assess eligibility for laser hair removal of health-care professionals and convolutional neural network (CNN)-based models.</p><p><strong>Results: </strong>The CNN ensemble model, synthesized from the outputs of five individual CNN models, reached an eligibility assessment accuracy of 0.52 (95% CI: 0.42-0.60) and a κ of 0.20 (95% CI: 0.13-0.27), taking a consensus expert label as reference. For comparison, board-certified dermatologists achieved a mean accuracy of 0.48 (95% CI: 0.44-0.52) and a mean κ of 0.26 (95% CI: 0.22-0.31). Intra-rater analysis of board-certified dermatologists yielded κ in the 0.32 (95% CI: 0.24-0.40) and 0.65 (95% CI: 0.56-0.74) range.</p><p><strong>Conclusion: </strong>Current assessment of eligibility for laser hair removal is challenging. Developing a laser hair removal eligibility assessment tool based on deep learning that performs on a par with trained dermatologists is feasible. Such a model may potentially reduce workload, increase quality and effectiveness, and facilitate equal health-care access. However, to achieve true clinical generalizability, prospective randomized clinical intervention studies are needed.</p>","PeriodicalId":17961,"journal":{"name":"Lasers in Surgery and Medicine","volume":" ","pages":""},"PeriodicalIF":2.2,"publicationDate":"2024-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142290322","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In Vivo Histological Study Evaluating Non-Ablative Fractional 1940-nm Laser. 评估 1940 纳米非烧蚀点阵激光的体内组织学研究
IF 2.2 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-15 DOI: 10.1002/lsm.23842
Konika Patel Schallen, Madelyn Seder, Michael Jorgenson, Kevin Schomacker, Jag Bhawan

Objectives: Non-ablative fractional lasers (NAFL) have increased in demand compared to ablative laser treatments as they provide lesser down time, fewer side-effects, and are safer to use. Non-ablative fractional treatment with lasers ranging from 1320 to 1927-nm have been shown to be safe and effective for skin resurfacing procedures. The objective of this study is to investigate healing of the 1940-nm NAFL-induced microthermal treatment zones (MTZs) in human skin from a histologic perspective.

Methods: Three subjects received 1940-nm NAFL treatment to test areas on the abdomen at various timepoints during the study. The minimum 5 mJ/MTZ and maximum 20 mJ/MTZ energy settings were used at 20% coverage. Biopsies were taken coinciding with immediately posttreatment, 1, 3, 7 days, and 6 weeks posttreatment. Blinded analysis of hematoxylin and eosin stained slides was performed to measure the width and depth of the MTZs and evaluate the inflammatory and healing response of the skin over time (immediately to 6 weeks posttreatment). Safety was evaluated by assessing local skin responses and adverse events immediately after treatment and at all study visits.

Results: Histological analysis of tissue following NAFL 1940-nm treatments showed mild early inflammatory response (presence of lymphotic infiltrate) in some test areas and zones of necrosis and coagulation having widths and depths (immediately-3 days posttreatment) that scaled with the 1940-nm pulse energy. Signs of healing such as presence of dermal mucin, evidence of fibrosis, and absence of necrosis were observed long-term (7 days to 6 weeks posttreatment). Evidence of the MTZ persisted beyond the 6-week study and was predicted to last for 100 days. All local clinical skin responses healed within 6 weeks and were limited to mild, transient erythema and edema which resolved in less than 12-24 h following treatment. No serious adverse events occurred during the study.

Conclusions: NAFL 1940-nm treatments are safe for inducing small fractional coagulation and necrosis zones in abdominal skin. NAFL 1940-nm laser creates fractional columns of injury with sufficient depth and coverage that suggest effective skin resurfacing, like other non-ablative fractional lasers.

目的:与烧蚀激光疗法相比,非烧蚀点阵激光疗法(NAFL)的停机时间更短、副作用更少、使用更安全,因此需求量越来越大。波长在 1320 到 1927 纳米之间的非烧蚀点阵激光治疗已被证明是安全有效的换肤疗法。本研究旨在从组织学角度研究1940-nm NAFL诱导的微热治疗区(MTZ)在人体皮肤中的愈合情况:方法:三名受试者在研究期间的不同时间点接受了腹部测试区域的 1940-nm NAFL 治疗。最小能量设置为 5 mJ/MTZ,最大能量设置为 20 mJ/MTZ,覆盖率为 20%。活组织切片的采集时间分别为治疗后即刻、治疗后 1 天、3 天、7 天和 6 周。对苏木精和伊红染色的切片进行盲法分析,以测量 MTZ 的宽度和深度,并评估随着时间推移(治疗后即刻至 6 周)皮肤的炎症和愈合反应。通过评估治疗后即刻和所有研究访问中的局部皮肤反应和不良反应,对安全性进行评估:NAFL 1940-nm 治疗后的组织学分析显示,一些测试区域出现轻微的早期炎症反应(存在淋巴浸润),坏死和凝固区的宽度和深度(治疗后 3 天内)与 1940-nm 脉冲能量成比例。长期(治疗后 7 天至 6 周)观察到愈合迹象,如真皮粘蛋白、纤维化迹象和无坏死。MTZ 的证据在 6 周的研究后仍然存在,预计将持续 100 天。所有局部临床皮肤反应均在 6 周内愈合,仅限于轻微、短暂的红斑和水肿,并在治疗后 12-24 小时内消退。研究期间未发生严重不良事件:结论:NAFL 1940-nm激光治疗对诱导腹部皮肤小面积凝固和坏死区是安全的。NAFL 1940-nm激光可形成具有足够深度和覆盖面的点阵损伤柱,与其他非烧蚀点阵激光一样,可有效换肤。
{"title":"In Vivo Histological Study Evaluating Non-Ablative Fractional 1940-nm Laser.","authors":"Konika Patel Schallen, Madelyn Seder, Michael Jorgenson, Kevin Schomacker, Jag Bhawan","doi":"10.1002/lsm.23842","DOIUrl":"https://doi.org/10.1002/lsm.23842","url":null,"abstract":"<p><strong>Objectives: </strong>Non-ablative fractional lasers (NAFL) have increased in demand compared to ablative laser treatments as they provide lesser down time, fewer side-effects, and are safer to use. Non-ablative fractional treatment with lasers ranging from 1320 to 1927-nm have been shown to be safe and effective for skin resurfacing procedures. The objective of this study is to investigate healing of the 1940-nm NAFL-induced microthermal treatment zones (MTZs) in human skin from a histologic perspective.</p><p><strong>Methods: </strong>Three subjects received 1940-nm NAFL treatment to test areas on the abdomen at various timepoints during the study. The minimum 5 mJ/MTZ and maximum 20 mJ/MTZ energy settings were used at 20% coverage. Biopsies were taken coinciding with immediately posttreatment, 1, 3, 7 days, and 6 weeks posttreatment. Blinded analysis of hematoxylin and eosin stained slides was performed to measure the width and depth of the MTZs and evaluate the inflammatory and healing response of the skin over time (immediately to 6 weeks posttreatment). Safety was evaluated by assessing local skin responses and adverse events immediately after treatment and at all study visits.</p><p><strong>Results: </strong>Histological analysis of tissue following NAFL 1940-nm treatments showed mild early inflammatory response (presence of lymphotic infiltrate) in some test areas and zones of necrosis and coagulation having widths and depths (immediately-3 days posttreatment) that scaled with the 1940-nm pulse energy. Signs of healing such as presence of dermal mucin, evidence of fibrosis, and absence of necrosis were observed long-term (7 days to 6 weeks posttreatment). Evidence of the MTZ persisted beyond the 6-week study and was predicted to last for 100 days. All local clinical skin responses healed within 6 weeks and were limited to mild, transient erythema and edema which resolved in less than 12-24 h following treatment. No serious adverse events occurred during the study.</p><p><strong>Conclusions: </strong>NAFL 1940-nm treatments are safe for inducing small fractional coagulation and necrosis zones in abdominal skin. NAFL 1940-nm laser creates fractional columns of injury with sufficient depth and coverage that suggest effective skin resurfacing, like other non-ablative fractional lasers.</p>","PeriodicalId":17961,"journal":{"name":"Lasers in Surgery and Medicine","volume":" ","pages":""},"PeriodicalIF":2.2,"publicationDate":"2024-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142290320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Is HMME-PDT the First Choice of Treatment for Young Children With Port-Wine Stain Birthmarks? HMME-PDT 是治疗患有葡萄酒胎记的幼儿的首选方法吗?
IF 2.2 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-15 DOI: 10.1002/lsm.23831
Jiang Xian
<p>Recently, Lasers in Surgery and Medicine published a meta-analysis based on 40 PDL studies and 18 HMME-PDT studies [<span>1</span>]. The authors indicate that “HMME-PDT has emerged as the first choice for PWB treatment, particularly for young children” and at the same time raise many questions regarding the use of HMME-PDT in China. On behalf of the Consensus Development Expert Group of Expert consensus on HMME-PDT, I appreciate American colleagues' interest and concern in HMME-PDT.</p><p>PDT's potential for PWS treatment was suggested in the mid-1980s and PDT protocols were developed for PWS treatment in China in the early 1990s [<span>2, 3</span>]. Two photosensitizing drugs, HiPorfin and Hemoporfin (also known as HMME) are approved for PWS treatment. There is no specific age restriction in HiPorfin production information. Because HMME Phase II and III trials only included patients > 14 years old, “lack of pediatric information in prescribe drug label” is stated in HMME production information. The post-marketing requirements suggest including pediatric patients in Phase IV trials to benefit them more. Clinical trials have been launched for 7−14 years old (NCT03125057, CTR20170189) and 2−7 years old (NCT04106258), respectively. Concerning “young children,” with therapeutic intention and on the premise of obtaining explicit informed consent from the parents, I believe the prescribing of HMME-PDT is regulatory adherence and in compliance with current regulations of rational off-label use of medicines [<span>4-6</span>].</p><p>The authors cite a paper published in 1934 and state that “hematoporphyrin derivatives have been used as antidepressants, indicating potential effects on brain function by this category of compounds. Therefore, the risk of HMME exposure to CNS in neonates, infants, and young children cannot be ignored.” In fact, the paper suggests it requires “intramuscular and oral administration of hematoporphyrin hydrochloride for an average period of 50 to 60 days” to see psychological benefit in depressive psychoses [<span>7</span>]. The remote risk of short-term HMME exposure to CNS in young children is likely small. Neurological and neuropsychiatric adverse reactions similar to that of porphyria have not been reported for HMME-PDT.</p><p>PDT was used before PDL became available in China. Partially due to this historical reason, many patients and parents would consider PDT as the first choice. For PDL resistance cases and large PWS lesions, clinicians might be inclined more toward PDT. But I am not aware that any publication implies “the use of HMME-PDT as the first choice of treatment for young children.” Hence, it is intriguing that the authors suggest that “HMME-PDT has emerged as the first choice for PWB in many major hospitals in China.” When accurate and thoughtfully presented, reporting of comparison of different modalities should be appreciated. In return, the authors who prefer one modality over another should have factua
最近,《激光在外科和医学中的应用》(Lasers in Surgery and Medicine)杂志发表了一项基于 40 项 PDL 研究和 18 项 HMME-PDT 研究的荟萃分析[1]。作者指出,"HMME-PDT 已成为 PWB 治疗的首选,尤其是对于幼儿",同时也对 HMME-PDT 在中国的使用提出了许多疑问。我代表HMME-PDT专家共识制定专家组,感谢美国同行对HMME-PDT的关注和关心。PDT治疗PWS的潜力早在20世纪80年代中期就被提出,20世纪90年代初中国就制定了PDT治疗PWS的方案[2, 3]。HiPorfin和Hemoporfin(又称HMME)这两种光敏药物被批准用于PWS治疗。HiPorfin的生产信息中没有具体的年龄限制。由于HMME的II期和III期试验只纳入了14岁的患者,因此在HMME的生产信息中注明了 "处方药标签中缺乏儿科信息"。上市后的要求建议将儿童患者纳入 IV 期试验,使他们更多受益。目前已分别启动了7-14岁(NCT03125057、CTR20170189)和2-7岁(NCT04106258)的临床试验。关于 "幼儿",在有治疗意图并获得家长明确知情同意的前提下,笔者认为开具HMME-PDT处方是合规的,符合目前合理标示外用药的规定[4-6]。作者引用了1934年发表的一篇论文,并指出:"血卟啉衍生物已被用作抗抑郁药,表明这类化合物对脑功能有潜在影响。因此,新生儿、婴幼儿接触 HMME 对中枢神经系统的风险不容忽视"。事实上,该论文认为,需要 "肌肉注射和口服盐酸血卟啉平均 50 到 60 天",才能看到抑郁性精神病患者的心理疗效[7]。短期接触 HMME 对幼儿中枢神经系统的远期风险可能很小。HMME-PDT尚未出现类似卟啉症的神经和神经精神不良反应。部分由于这一历史原因,许多患者和家长将 PDT 作为首选。对于PDL耐药病例和大面积PWS病变,临床医生可能更倾向于PDT。但我并不知道有任何出版物暗示 "HMME-PDT 是幼儿治疗的首选"。因此,作者认为 "HMME-PDT已成为中国许多大医院治疗PWB的首选",这一点很耐人寻味。如果报告准确且经过深思熟虑,对不同模式进行比较的报告应该受到赞赏。反过来,偏爱某种治疗方法的作者也应做到事实准确,适当、平衡地考虑支持或反对某种治疗方法的可信证据。遗憾的是,大量文章都是以观点而非事实为基础。在我看来,两组人的许多数据集和基线并不完全可比。不过,只要解释了分析的局限性,并非常谨慎地解释结果,这种情况是可以接受的。毫无疑问,我们不能仅凭一项荟萃分析就得出是否应将 PDT 作为首选的结论。尽管如此,为了确保 HMME-PDT 的安全、一致和正确使用,我们还是根据《医疗实践指南报告项目》(RIGHT)编制了《HMME-PDT 治疗葡萄酒港污渍的专家共识(2024)》,并在国际实践指南注册平台(PREPARE-2022CN610)上进行了注册[8]。我们期待与美国同行就 HMME-PDT 进行深入讨论。
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引用次数: 0
The Implication of Photodynamic Therapy Applied to the Level of Tumor Resection on Postoperative Cerebral Edema and Intracranial Pressure Changes in Gliomas 应用于肿瘤切除层面的光动力疗法对胶质瘤术后脑水肿和颅内压变化的影响
IF 2.2 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-10 DOI: 10.1002/lsm.23837
Jingxuan Li, Weijun Sun, Shaoshan Hu, Xiuwei Yan

Aim

The aim of our study was to explore the factors influencing cerebral edema and intracranial pressure in glioblastoma multiforme (GBM) patients who undergo photodynamic therapy (PDT) after resection.

Approach

This was a retrospective controlled study of GBM patients treated with PDT-assisted resections of varying scope from May 2021 to August 2023. The baseline clinical data, cerebral edema volumes, intracranial pressure values, and imaging data of the GBM patients were collected for statistical analysis.

Results

A total of 56 GBM patients were included. Thirty of the patients underwent gross total resection (GTR), and the other 26 patients underwent subtotal resection (STR). We found that the cerebral edema volume and the mean intracranial pressure in patients who underwent GTR were lower than those in patients who underwent STR. Moreover, univariate analysis showed that the scope of tumor resection was an independent factor affecting cerebral edema and intracranial pressure after PDT.

Conclusions

Compared with STR, PDT combined with GTR significantly reduced postoperative brain edema volume and intracranial pressure in GBM patients.

目的 我们的研究旨在探讨多形性胶质母细胞瘤(GBM)患者切除术后接受光动力疗法(PDT)的脑水肿和颅内压的影响因素。研究收集了GBM患者的基线临床数据、脑水肿体积、颅内压值和影像学数据,并进行了统计分析。其中 30 名患者接受了全切术(GTR),另外 26 名患者接受了次全切术(STR)。我们发现,GTR 患者的脑水肿体积和平均颅内压均低于 STR 患者。此外,单变量分析表明,肿瘤切除范围是影响 PDT 术后脑水肿和颅内压的独立因素。
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引用次数: 0
Effects of Cryolipolysis on the Conversion of White Adipose Tissue: Pilot Study 冷冻溶脂对白色脂肪组织转化的影响:试点研究
IF 2.4 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-09-10 DOI: 10.1002/lsm.23839
Christiane Rodrigues Tofoli Palauro, Patrícia Froes Meyer, Ciro Dantas Soares, Eneida de Morais Carreiro, Flávio de Paiva Dumaresq, Fernando Cesar Camara de Oliveira, Ana Laura Martins de Andrade, Priscila da S. P. S. Daumas
IntroductionCryolipolysis (CLL) is a widely employed noninvasive procedure for body fat reduction. It operates by inducing cooling, leading to the crystallization of cytoplasmic lipids, loss of cellular integrity, and apoptosis/necrosis of adipocytes, accompanied by local inflammation. Ongoing discussions revolve around CLL's potential to transform white adipocytes into brown adipocytes, potentially yielding more significant effects compared to alternative procedures.ObjectiveThus, this randomized, blinded clinical study aimed to investigate the effects of CLL on adipose tissue and elucidate the mechanisms involved in its application and capacity for adipocyte conversion.MethodologyTissue samples from six patients were assessed at intervals of 45, 60, and 90 days following the application of the CLL protocol during abdominoplasty surgeries.ResultsThe samples underwent immunohistochemical analyses targeting various markers, revealing higher expression of PPAR‐gamma, PPAR‐alpha, and UCP‐1 markers in CLL‐treated samples.ConclusionTherefore, the present study suggests that CLL has the ability to intervene in adipocyte conversion.
导言冷冻溶脂(CLL)是一种广泛采用的非侵入性减脂方法。其原理是通过冷却,使细胞质脂质结晶、细胞完整性丧失、脂肪细胞凋亡/坏死,并伴有局部炎症。因此,这项随机、盲法临床研究旨在调查 CLL 对脂肪组织的影响,并阐明其应用机制和脂肪细胞转化能力。方法在腹部整形手术中应用 CLL 方案后,分别在 45 天、60 天和 90 天对六名患者的组织样本进行评估。结果对样本进行了针对各种标记物的免疫组化分析,结果显示在 CLL 处理的样本中 PPAR-γ、PPAR-α 和 UCP-1 标记物的表达较高。
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引用次数: 0
期刊
Lasers in Surgery and Medicine
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