部分取样薄黑色素瘤的重新活检影响前哨淋巴结取样和手术边缘。

IF 1 Q4 ONCOLOGY
Melanoma Management Pub Date : 2019-04-26 eCollection Date: 2019-06-01 DOI:10.2217/mmt-2018-0011
Evan S Weitman, Matthew C Perez, Daniel Lee, Youngchul Kim, William Fulp, Vernon K Sondak, Amod A Sarnaik, Ricardo J Gonzalez, Carl W Cruse, Jane L Messina, Jonathan S Zager
{"title":"部分取样薄黑色素瘤的重新活检影响前哨淋巴结取样和手术边缘。","authors":"Evan S Weitman,&nbsp;Matthew C Perez,&nbsp;Daniel Lee,&nbsp;Youngchul Kim,&nbsp;William Fulp,&nbsp;Vernon K Sondak,&nbsp;Amod A Sarnaik,&nbsp;Ricardo J Gonzalez,&nbsp;Carl W Cruse,&nbsp;Jane L Messina,&nbsp;Jonathan S Zager","doi":"10.2217/mmt-2018-0011","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>To assess the impact of re-biopsy on partially sampled melanoma <i>in situ</i> (MIS), atypical melanocytic proliferation (AMP) and thin invasive melanoma.</p><p><strong>Materials & methods: </strong>We retrospectively identified cases of re-biopsied partially sampled neoplasms initially diagnosed as melanoma <i>in situ</i>, AMP or thin melanoma (Breslow depth ≤0.75 mm).</p><p><strong>Results & conclusion: </strong>Re-biopsy led to sentinel lymph node biopsy (SLNB) in 18.3% of cases. No patients upstaged from AMP or MIS had a positive SLNB. One out of nine (11.1%) initially diagnosed as a thin melanoma ≤0.75 mm, upstaged with a re-biopsy, had a positive SLNB. After re-biopsy 8.5% underwent an increased surgical margin. Selective re-biopsy of partially sampled melanoma with gross residual disease can increase the accuracy of microstaging and optimize treatment regarding surgical margins and SLNB.</p>","PeriodicalId":44562,"journal":{"name":"Melanoma Management","volume":null,"pages":null},"PeriodicalIF":1.0000,"publicationDate":"2019-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/mmt-2018-0011","citationCount":"1","resultStr":"{\"title\":\"Re-biopsy of partially sampled thin melanoma impacts sentinel lymph node sampling as well as surgical margins.\",\"authors\":\"Evan S Weitman,&nbsp;Matthew C Perez,&nbsp;Daniel Lee,&nbsp;Youngchul Kim,&nbsp;William Fulp,&nbsp;Vernon K Sondak,&nbsp;Amod A Sarnaik,&nbsp;Ricardo J Gonzalez,&nbsp;Carl W Cruse,&nbsp;Jane L Messina,&nbsp;Jonathan S Zager\",\"doi\":\"10.2217/mmt-2018-0011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aim: </strong>To assess the impact of re-biopsy on partially sampled melanoma <i>in situ</i> (MIS), atypical melanocytic proliferation (AMP) and thin invasive melanoma.</p><p><strong>Materials & methods: </strong>We retrospectively identified cases of re-biopsied partially sampled neoplasms initially diagnosed as melanoma <i>in situ</i>, AMP or thin melanoma (Breslow depth ≤0.75 mm).</p><p><strong>Results & conclusion: </strong>Re-biopsy led to sentinel lymph node biopsy (SLNB) in 18.3% of cases. No patients upstaged from AMP or MIS had a positive SLNB. One out of nine (11.1%) initially diagnosed as a thin melanoma ≤0.75 mm, upstaged with a re-biopsy, had a positive SLNB. After re-biopsy 8.5% underwent an increased surgical margin. Selective re-biopsy of partially sampled melanoma with gross residual disease can increase the accuracy of microstaging and optimize treatment regarding surgical margins and SLNB.</p>\",\"PeriodicalId\":44562,\"journal\":{\"name\":\"Melanoma Management\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2019-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.2217/mmt-2018-0011\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Melanoma Management\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2217/mmt-2018-0011\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2019/6/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Melanoma Management","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2217/mmt-2018-0011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/6/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 1

摘要

目的:评估重新活检对部分取样原位黑色素瘤(MIS)、非典型黑色素细胞增殖(AMP)和薄侵袭性黑色素瘤的影响。材料与方法:我们回顾性地确定了一些重新活检的部分取样肿瘤,最初诊断为原位黑色素瘤、AMP或薄黑色素瘤(Breslow深度≤0.75 mm)。结果与结论:18.3%的病例重新活检导致前哨淋巴结活组织检查(SLNB)。从AMP或MIS中抢出来的患者没有SLNB阳性。九分之一(11.1%)最初诊断为≤0.75 mm的薄黑色素瘤,经重新活检后,SLNB呈阳性。再次活检后,8.5%的患者手术切缘增加。对部分采样的伴有严重残留疾病的黑色素瘤进行选择性重新活检可以提高显微分期的准确性,并优化手术边缘和SLNB的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Re-biopsy of partially sampled thin melanoma impacts sentinel lymph node sampling as well as surgical margins.

Aim: To assess the impact of re-biopsy on partially sampled melanoma in situ (MIS), atypical melanocytic proliferation (AMP) and thin invasive melanoma.

Materials & methods: We retrospectively identified cases of re-biopsied partially sampled neoplasms initially diagnosed as melanoma in situ, AMP or thin melanoma (Breslow depth ≤0.75 mm).

Results & conclusion: Re-biopsy led to sentinel lymph node biopsy (SLNB) in 18.3% of cases. No patients upstaged from AMP or MIS had a positive SLNB. One out of nine (11.1%) initially diagnosed as a thin melanoma ≤0.75 mm, upstaged with a re-biopsy, had a positive SLNB. After re-biopsy 8.5% underwent an increased surgical margin. Selective re-biopsy of partially sampled melanoma with gross residual disease can increase the accuracy of microstaging and optimize treatment regarding surgical margins and SLNB.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.10
自引率
0.00%
发文量
4
审稿时长
13 weeks
期刊介绍: Skin cancer is on the rise. According to the World Health Organization, 132,000 melanoma skin cancers occur globally each year. While early-stage melanoma is usually relatively easy to treat, once disease spreads prognosis worsens considerably. Therefore, research into combating advanced-stage melanoma is a high priority. New and emerging therapies, such as monoclonal antibodies, B-RAF and KIT inhibitors, antiangiogenic agents and novel chemotherapy approaches hold promise for prolonging survival, but the search for a cure is ongoing. Melanoma Management publishes high-quality peer-reviewed articles on all aspects of melanoma, from prevention to diagnosis and from treatment of early-stage disease to late-stage melanoma and metastasis. The journal presents the latest research findings in melanoma research and treatment, together with authoritative reviews, cutting-edge editorials and perspectives that highlight hot topics and controversy in the field. Independent drug evaluations assess newly approved medications and their role in clinical practice. Key topics covered include: Risk factors, prevention and sun safety education Diagnosis, staging and grading Surgical excision of melanoma lesions Sentinel lymph node biopsy Biological therapies, including immunotherapy and vaccination Novel chemotherapy options Treatment of metastasis Prevention of recurrence Patient care and quality of life.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信