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Genomic Landscape of Spitzoid Neoplasms Impacting Patient Management
Spitzoid neoplasms are a distinct group of melanocytic proliferations characterized by epithelioid and/ or spindle shaped melanocytes. Intermediate forms that share features of both benign Spitz nevi (SN) and Spitz melanoma, i.e., malignant Spitz tumor (MST) represent a diagnostically and clinically...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300473/ https://www.ncbi.nlm.nih.gov/pubmed/30619857 http://dx.doi.org/10.3389/fmed.2018.00344 |
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author | Hillen, Lisa M. Van den Oord, Joost Geybels, Milan S. Becker, Jürgen C. zur Hausen, Axel Winnepenninckx, Véronique |
author_facet | Hillen, Lisa M. Van den Oord, Joost Geybels, Milan S. Becker, Jürgen C. zur Hausen, Axel Winnepenninckx, Véronique |
author_sort | Hillen, Lisa M. |
collection | PubMed |
description | Spitzoid neoplasms are a distinct group of melanocytic proliferations characterized by epithelioid and/ or spindle shaped melanocytes. Intermediate forms that share features of both benign Spitz nevi (SN) and Spitz melanoma, i.e., malignant Spitz tumor (MST) represent a diagnostically and clinically challenging group of melanocytic lesions. A multitude of descriptive diagnostic terms exist for these ambiguous lesions with atypical Spitz tumor (AST) or Spitz tumor of uncertain malignant potential (STUMP) just naming two of them. This diagnostic gray zone creates confusion and high insecurity in clinicians and in patients. Biological behavior and clinical course of this intermediate group still remains largely unknown, often leading to difficulties with uncertainties in clinical management and prognosis. Consequently, a better stratification of Spitzoid neoplasms in benign and malignant forms is required thereby keeping the diagnostic group of AST/STUMP as small as possible. Ancillary diagnostic techniques such as immunohistochemistry, comparative genomic hybridization, fluorescence in situ hybridization, next generation sequencing, micro RNA and mRNA analysis as well as mass spectrometry imaging offer new opportunities for the distinct diagnosis, thereby allowing the best clinical management of Spitzoid neoplasms. This review gives an overview on these additional diagnostic techniques and the recent developments in the field of molecular genetic alterations in Spitzoid neoplasms. We also discuss how the recent findings might facilitate the diagnosis and stratification of atypical Spitzoid neoplasms and how these findings will impact the diagnostic work up as well as patient management. We suggest a stepwise implementation of ancillary diagnostic techniques thereby integrating immunohistochemistry and molecular pathology findings in the diagnosis of challenging ambiguous Spitzoid neoplasms. Finally, we will give an outlook on pending future research objectives in the field of Spitzoid melanocytic lesions. |
format | Online Article Text |
id | pubmed-6300473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63004732019-01-07 Genomic Landscape of Spitzoid Neoplasms Impacting Patient Management Hillen, Lisa M. Van den Oord, Joost Geybels, Milan S. Becker, Jürgen C. zur Hausen, Axel Winnepenninckx, Véronique Front Med (Lausanne) Medicine Spitzoid neoplasms are a distinct group of melanocytic proliferations characterized by epithelioid and/ or spindle shaped melanocytes. Intermediate forms that share features of both benign Spitz nevi (SN) and Spitz melanoma, i.e., malignant Spitz tumor (MST) represent a diagnostically and clinically challenging group of melanocytic lesions. A multitude of descriptive diagnostic terms exist for these ambiguous lesions with atypical Spitz tumor (AST) or Spitz tumor of uncertain malignant potential (STUMP) just naming two of them. This diagnostic gray zone creates confusion and high insecurity in clinicians and in patients. Biological behavior and clinical course of this intermediate group still remains largely unknown, often leading to difficulties with uncertainties in clinical management and prognosis. Consequently, a better stratification of Spitzoid neoplasms in benign and malignant forms is required thereby keeping the diagnostic group of AST/STUMP as small as possible. Ancillary diagnostic techniques such as immunohistochemistry, comparative genomic hybridization, fluorescence in situ hybridization, next generation sequencing, micro RNA and mRNA analysis as well as mass spectrometry imaging offer new opportunities for the distinct diagnosis, thereby allowing the best clinical management of Spitzoid neoplasms. This review gives an overview on these additional diagnostic techniques and the recent developments in the field of molecular genetic alterations in Spitzoid neoplasms. We also discuss how the recent findings might facilitate the diagnosis and stratification of atypical Spitzoid neoplasms and how these findings will impact the diagnostic work up as well as patient management. We suggest a stepwise implementation of ancillary diagnostic techniques thereby integrating immunohistochemistry and molecular pathology findings in the diagnosis of challenging ambiguous Spitzoid neoplasms. Finally, we will give an outlook on pending future research objectives in the field of Spitzoid melanocytic lesions. Frontiers Media S.A. 2018-12-13 /pmc/articles/PMC6300473/ /pubmed/30619857 http://dx.doi.org/10.3389/fmed.2018.00344 Text en Copyright © 2018 Hillen, Van den Oord, Geybels, Becker, zur Hausen and Winnepenninckx. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Hillen, Lisa M. Van den Oord, Joost Geybels, Milan S. Becker, Jürgen C. zur Hausen, Axel Winnepenninckx, Véronique Genomic Landscape of Spitzoid Neoplasms Impacting Patient Management |
title | Genomic Landscape of Spitzoid Neoplasms Impacting Patient Management |
title_full | Genomic Landscape of Spitzoid Neoplasms Impacting Patient Management |
title_fullStr | Genomic Landscape of Spitzoid Neoplasms Impacting Patient Management |
title_full_unstemmed | Genomic Landscape of Spitzoid Neoplasms Impacting Patient Management |
title_short | Genomic Landscape of Spitzoid Neoplasms Impacting Patient Management |
title_sort | genomic landscape of spitzoid neoplasms impacting patient management |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300473/ https://www.ncbi.nlm.nih.gov/pubmed/30619857 http://dx.doi.org/10.3389/fmed.2018.00344 |
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