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Standardized diagnostic algorithm for spitzoid lesions aids clinical decision-making and management: a case series from a Swiss reference center

Importance: Spitzoid lesions are a group of melanocytic tumors characterized by spindle-like or epithelioid cells with variable malignant potential. While some spitzoid lesions are classified as evidently benign or malignant by clinic and histology, others present with unclear clinical and histologi...

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Autores principales: Hilbers, Marie-Luise, Brändli, Regula, Mühleisen, Beda, Freiberger, Sandra N., Mangana, Joanna, Dummer, Reinhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825637/
https://www.ncbi.nlm.nih.gov/pubmed/33520116
http://dx.doi.org/10.18632/oncotarget.27854
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author Hilbers, Marie-Luise
Brändli, Regula
Mühleisen, Beda
Freiberger, Sandra N.
Mangana, Joanna
Dummer, Reinhard
author_facet Hilbers, Marie-Luise
Brändli, Regula
Mühleisen, Beda
Freiberger, Sandra N.
Mangana, Joanna
Dummer, Reinhard
author_sort Hilbers, Marie-Luise
collection PubMed
description Importance: Spitzoid lesions are a group of melanocytic tumors characterized by spindle-like or epithelioid cells with variable malignant potential. While some spitzoid lesions are classified as evidently benign or malignant by clinic and histology, others present with unclear clinical and histological characteristics and are categorized as lesions of intermediate biologic potential. These lesions represent a challenge for pathologists and clinicians alike. No consensus on ancillary diagnostics and clinical management exists. Prediction of their clinical course is difficult. The implementation of ancillary diagnostics is currently subject of extensive discussions. Observations: We report three cases of spitzoid lesions in three young female patients (3-, 15- and 17 years old) from a single reference center with different clinical and histological manifestations. In each case, uncertain clinical and histological presentation led to the stepwise application of additional diagnostics using immunohistochemistry and a custom next generation sequencing panel optimized for melanocytic lesions (MelArray). Combining ancillary diagnostics helped determine clinical management in all cases by characterizing the biology of these lesions. Conclusions and Relevance: We illustrate how clinical, histological and molecular features contribute to an optimized management plan in these critical situations and present a possible algorithm for the assessment of spitzoid neoplasms.
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spelling pubmed-78256372021-01-29 Standardized diagnostic algorithm for spitzoid lesions aids clinical decision-making and management: a case series from a Swiss reference center Hilbers, Marie-Luise Brändli, Regula Mühleisen, Beda Freiberger, Sandra N. Mangana, Joanna Dummer, Reinhard Oncotarget Case Report Importance: Spitzoid lesions are a group of melanocytic tumors characterized by spindle-like or epithelioid cells with variable malignant potential. While some spitzoid lesions are classified as evidently benign or malignant by clinic and histology, others present with unclear clinical and histological characteristics and are categorized as lesions of intermediate biologic potential. These lesions represent a challenge for pathologists and clinicians alike. No consensus on ancillary diagnostics and clinical management exists. Prediction of their clinical course is difficult. The implementation of ancillary diagnostics is currently subject of extensive discussions. Observations: We report three cases of spitzoid lesions in three young female patients (3-, 15- and 17 years old) from a single reference center with different clinical and histological manifestations. In each case, uncertain clinical and histological presentation led to the stepwise application of additional diagnostics using immunohistochemistry and a custom next generation sequencing panel optimized for melanocytic lesions (MelArray). Combining ancillary diagnostics helped determine clinical management in all cases by characterizing the biology of these lesions. Conclusions and Relevance: We illustrate how clinical, histological and molecular features contribute to an optimized management plan in these critical situations and present a possible algorithm for the assessment of spitzoid neoplasms. Impact Journals LLC 2021-01-19 /pmc/articles/PMC7825637/ /pubmed/33520116 http://dx.doi.org/10.18632/oncotarget.27854 Text en Copyright: © 2021 Hilbers et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Hilbers, Marie-Luise
Brändli, Regula
Mühleisen, Beda
Freiberger, Sandra N.
Mangana, Joanna
Dummer, Reinhard
Standardized diagnostic algorithm for spitzoid lesions aids clinical decision-making and management: a case series from a Swiss reference center
title Standardized diagnostic algorithm for spitzoid lesions aids clinical decision-making and management: a case series from a Swiss reference center
title_full Standardized diagnostic algorithm for spitzoid lesions aids clinical decision-making and management: a case series from a Swiss reference center
title_fullStr Standardized diagnostic algorithm for spitzoid lesions aids clinical decision-making and management: a case series from a Swiss reference center
title_full_unstemmed Standardized diagnostic algorithm for spitzoid lesions aids clinical decision-making and management: a case series from a Swiss reference center
title_short Standardized diagnostic algorithm for spitzoid lesions aids clinical decision-making and management: a case series from a Swiss reference center
title_sort standardized diagnostic algorithm for spitzoid lesions aids clinical decision-making and management: a case series from a swiss reference center
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825637/
https://www.ncbi.nlm.nih.gov/pubmed/33520116
http://dx.doi.org/10.18632/oncotarget.27854
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