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Sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma

Squamous cell carcinomas are among the most common skin tumors and show a risk of metastasis depending on various factors such as tumor thickness, localization, histological subtype and immune status of the patient. Sentinel lymph node biopsy (SLNB) SLNB represents a possibility for assessing the lo...

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Autores principales: Kofler, Lukas, Kofler, Katrin, Schulz, Claudia, Breuninger, Helmut, Häfner, Hans-Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864829/
https://www.ncbi.nlm.nih.gov/pubmed/32385689
http://dx.doi.org/10.1007/s00403-020-02082-1
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author Kofler, Lukas
Kofler, Katrin
Schulz, Claudia
Breuninger, Helmut
Häfner, Hans-Martin
author_facet Kofler, Lukas
Kofler, Katrin
Schulz, Claudia
Breuninger, Helmut
Häfner, Hans-Martin
author_sort Kofler, Lukas
collection PubMed
description Squamous cell carcinomas are among the most common skin tumors and show a risk of metastasis depending on various factors such as tumor thickness, localization, histological subtype and immune status of the patient. Sentinel lymph node biopsy (SLNB) SLNB represents a possibility for assessing the locoregional lymph node status. In this study, the role of the SLNB in lymph node status and survival was analyzed. Retrospectively, 720 patients with high-risk squamous cell carcinoma (tumor thickness > 5 mm) were examined. 150 patients agreed to SLNB, 570 patients did not undergo histologic confirmation of lymph node status and were included directly in follow-up. In 101 patients, a sentinel lymph node was successfully marked and extirpated, followed by regular follow-up examinations. A total of 11.11% of the patients showed lymph node metastasis in the course of their treatment, with no difference in the proportion of patients in the SLNB group (11.9%) and the observation group (11.4%) (p = 0.873). The proportion of distant metastasis also did not differ between the groups (p = 0.898). In 3.96% of the patients in the SLNB group, a metastasis was found in the sentinel lymph node. Tumor-specific death was observed in 7.14% of the patients in the SLNB group and 4.74% in the observation group (p = 0.269). Although SLNB is a principally suitable method for determining lymph node status, the available data do not provide any benefit regarding further metastasis or tumor-specific survival.
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spelling pubmed-78648292021-02-16 Sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma Kofler, Lukas Kofler, Katrin Schulz, Claudia Breuninger, Helmut Häfner, Hans-Martin Arch Dermatol Res Original Paper Squamous cell carcinomas are among the most common skin tumors and show a risk of metastasis depending on various factors such as tumor thickness, localization, histological subtype and immune status of the patient. Sentinel lymph node biopsy (SLNB) SLNB represents a possibility for assessing the locoregional lymph node status. In this study, the role of the SLNB in lymph node status and survival was analyzed. Retrospectively, 720 patients with high-risk squamous cell carcinoma (tumor thickness > 5 mm) were examined. 150 patients agreed to SLNB, 570 patients did not undergo histologic confirmation of lymph node status and were included directly in follow-up. In 101 patients, a sentinel lymph node was successfully marked and extirpated, followed by regular follow-up examinations. A total of 11.11% of the patients showed lymph node metastasis in the course of their treatment, with no difference in the proportion of patients in the SLNB group (11.9%) and the observation group (11.4%) (p = 0.873). The proportion of distant metastasis also did not differ between the groups (p = 0.898). In 3.96% of the patients in the SLNB group, a metastasis was found in the sentinel lymph node. Tumor-specific death was observed in 7.14% of the patients in the SLNB group and 4.74% in the observation group (p = 0.269). Although SLNB is a principally suitable method for determining lymph node status, the available data do not provide any benefit regarding further metastasis or tumor-specific survival. Springer Berlin Heidelberg 2020-05-08 2021 /pmc/articles/PMC7864829/ /pubmed/32385689 http://dx.doi.org/10.1007/s00403-020-02082-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Paper
Kofler, Lukas
Kofler, Katrin
Schulz, Claudia
Breuninger, Helmut
Häfner, Hans-Martin
Sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma
title Sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma
title_full Sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma
title_fullStr Sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma
title_full_unstemmed Sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma
title_short Sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma
title_sort sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864829/
https://www.ncbi.nlm.nih.gov/pubmed/32385689
http://dx.doi.org/10.1007/s00403-020-02082-1
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