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How Should We Treat Meningeal Melanocytoma? A Retrospective Analysis of Potential Treatment Strategies

SIMPLE SUMMARY: As a rare tumor disease, only single case reports and small case series have been published on meningeal melanocytomas. In the case of complete surgical resection, there is a shallow risk of recurrence, whereas the benefit of radiotherapy or chemotherapy, both as single or combined t...

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Autores principales: Ricchizzi, Sarah, Gallus, Marco, Stummer, Walter, Holling, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738837/
https://www.ncbi.nlm.nih.gov/pubmed/36497333
http://dx.doi.org/10.3390/cancers14235851
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author Ricchizzi, Sarah
Gallus, Marco
Stummer, Walter
Holling, Markus
author_facet Ricchizzi, Sarah
Gallus, Marco
Stummer, Walter
Holling, Markus
author_sort Ricchizzi, Sarah
collection PubMed
description SIMPLE SUMMARY: As a rare tumor disease, only single case reports and small case series have been published on meningeal melanocytomas. In the case of complete surgical resection, there is a shallow risk of recurrence, whereas the benefit of radiotherapy or chemotherapy, both as single or combined therapy, is unclear. This work aims to analyze and summarize previously published cases and proposes a therapeutic algorithm. ABSTRACT: Background: Meningeal melanocytomas (MM) are rare primary melanocytic tumors of the leptomeninges with an incidence of 1:10,000,000. Until now, there has been only sparse information about this tumor entity. Here, we provide a meta-analysis of all cases published in the English language since 1972. Methods: A literature review was performed using PubMed and Web of Science. All published cases were evaluated for location, sex, age, therapeutic approach, and outcome. In total, we included 201 patient cases in our meta–analysis. Results: The majority of MM was diagnosed more frequently in men between the third and fifth decade of life. Surgery is the preferred therapeutic approach, and total resection is associated with the best outcome. Patients with partial resection or tumor recurrence benefit from adjuvant radiotherapy, whereas chemo- or immunotherapies do not improve the disease course. Malignant transformation was described in 18 patients. Of these, 11 patients developed metastasis. Conclusions: We present the first retrospective meta-analysis of all MM cases published in the English language, including an evaluation of different treatment strategies allowing us to suggest a novel treatment guideline highlighting the importance of total resection for recurrence–free survival and characterizing those cases which benefit from adjuvant radiotherapy.
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spelling pubmed-97388372022-12-11 How Should We Treat Meningeal Melanocytoma? A Retrospective Analysis of Potential Treatment Strategies Ricchizzi, Sarah Gallus, Marco Stummer, Walter Holling, Markus Cancers (Basel) Article SIMPLE SUMMARY: As a rare tumor disease, only single case reports and small case series have been published on meningeal melanocytomas. In the case of complete surgical resection, there is a shallow risk of recurrence, whereas the benefit of radiotherapy or chemotherapy, both as single or combined therapy, is unclear. This work aims to analyze and summarize previously published cases and proposes a therapeutic algorithm. ABSTRACT: Background: Meningeal melanocytomas (MM) are rare primary melanocytic tumors of the leptomeninges with an incidence of 1:10,000,000. Until now, there has been only sparse information about this tumor entity. Here, we provide a meta-analysis of all cases published in the English language since 1972. Methods: A literature review was performed using PubMed and Web of Science. All published cases were evaluated for location, sex, age, therapeutic approach, and outcome. In total, we included 201 patient cases in our meta–analysis. Results: The majority of MM was diagnosed more frequently in men between the third and fifth decade of life. Surgery is the preferred therapeutic approach, and total resection is associated with the best outcome. Patients with partial resection or tumor recurrence benefit from adjuvant radiotherapy, whereas chemo- or immunotherapies do not improve the disease course. Malignant transformation was described in 18 patients. Of these, 11 patients developed metastasis. Conclusions: We present the first retrospective meta-analysis of all MM cases published in the English language, including an evaluation of different treatment strategies allowing us to suggest a novel treatment guideline highlighting the importance of total resection for recurrence–free survival and characterizing those cases which benefit from adjuvant radiotherapy. MDPI 2022-11-27 /pmc/articles/PMC9738837/ /pubmed/36497333 http://dx.doi.org/10.3390/cancers14235851 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ricchizzi, Sarah
Gallus, Marco
Stummer, Walter
Holling, Markus
How Should We Treat Meningeal Melanocytoma? A Retrospective Analysis of Potential Treatment Strategies
title How Should We Treat Meningeal Melanocytoma? A Retrospective Analysis of Potential Treatment Strategies
title_full How Should We Treat Meningeal Melanocytoma? A Retrospective Analysis of Potential Treatment Strategies
title_fullStr How Should We Treat Meningeal Melanocytoma? A Retrospective Analysis of Potential Treatment Strategies
title_full_unstemmed How Should We Treat Meningeal Melanocytoma? A Retrospective Analysis of Potential Treatment Strategies
title_short How Should We Treat Meningeal Melanocytoma? A Retrospective Analysis of Potential Treatment Strategies
title_sort how should we treat meningeal melanocytoma? a retrospective analysis of potential treatment strategies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738837/
https://www.ncbi.nlm.nih.gov/pubmed/36497333
http://dx.doi.org/10.3390/cancers14235851
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