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Sporadic spinal psammomatous malignant melanotic nerve sheath tumor: A case report and literature review

BACKGROUND: Sporadic Spinal Psammomatous Malignant Melanotic Nerve Sheath Tumor (SSP-MMNST) is a rare subgroup of peripheral nerve sheath tumors arising along the spine. Only a few reports of SSP-MMNST have been described. In this paper, we review the literature on SSP-MMNST focusing on clinical, an...

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Autores principales: Bonomo, Giulio, Gans, Alessandro, Mazzapicchi, Elio, Rubiu, Emanuele, Alimonti, Paolo, Eoli, Marica, Paterra, Rosina, Pollo, Bianca, Iess, Guglielmo, Restelli, Francesco, Falco, Jacopo, Acerbi, Francesco, Schiariti, Marco Paolo, Ferroli, Paolo, Broggi, Morgan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998981/
https://www.ncbi.nlm.nih.gov/pubmed/36910634
http://dx.doi.org/10.3389/fonc.2023.1100532
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author Bonomo, Giulio
Gans, Alessandro
Mazzapicchi, Elio
Rubiu, Emanuele
Alimonti, Paolo
Eoli, Marica
Paterra, Rosina
Pollo, Bianca
Iess, Guglielmo
Restelli, Francesco
Falco, Jacopo
Acerbi, Francesco
Schiariti, Marco Paolo
Ferroli, Paolo
Broggi, Morgan
author_facet Bonomo, Giulio
Gans, Alessandro
Mazzapicchi, Elio
Rubiu, Emanuele
Alimonti, Paolo
Eoli, Marica
Paterra, Rosina
Pollo, Bianca
Iess, Guglielmo
Restelli, Francesco
Falco, Jacopo
Acerbi, Francesco
Schiariti, Marco Paolo
Ferroli, Paolo
Broggi, Morgan
author_sort Bonomo, Giulio
collection PubMed
description BACKGROUND: Sporadic Spinal Psammomatous Malignant Melanotic Nerve Sheath Tumor (SSP-MMNST) is a rare subgroup of peripheral nerve sheath tumors arising along the spine. Only a few reports of SSP-MMNST have been described. In this paper, we review the literature on SSP-MMNST focusing on clinical, and diagnostic features, as well as investigating possible pathogenetic mechanisms to better implement therapeutic strategies. We also report an illustrative case of a young female presenting with cervicobrachial pain due to two SSP-MMNSTs arising from C5-6 right spinal roots. CASE DESCRIPTION: We report a case of a 28-year-old woman presenting with right arm weakness and dysesthesia. Clinical examination and neuroimaging were performed, and, following surgical removal of both lesions, a histological diagnosis of SSP-MMNST was obtained. RESULTS: The literature review identified 21 eligible studies assessing 23 patients with SSP-MMNST, with a mean onset age of 41 years and a slight male gender preference. The lumbar district was the most involved spinal segment. Gross-total resection (GTR) was the treatment of choice in all amenable cases, followed in selected cases with residual tumor by adjuvant radiotherapy or chemotherapy. The metastatic and recurrence rates were 31.58% and 36.8%, respectively. CONCLUSION: Differently from common schwannomas, MMNST represents a rare disease with known recurrence and metastatization propensity. As reported in our review, SSP-MMNST has a greater recurrence rate when compared to other forms of spinal MMNST, raising questions about the greater aggressiveness of the former. We also found that residual disease is related to a higher risk of systemic disease spreading. This metastatic potential, usually associated with primary lumbar localization, is characterized by a slight male prevalence. Indeed, whenever GTR is unachievable, considering the higher recurrence rate, adjuvant radiation therapy should be taken into consideration.
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spelling pubmed-99989812023-03-11 Sporadic spinal psammomatous malignant melanotic nerve sheath tumor: A case report and literature review Bonomo, Giulio Gans, Alessandro Mazzapicchi, Elio Rubiu, Emanuele Alimonti, Paolo Eoli, Marica Paterra, Rosina Pollo, Bianca Iess, Guglielmo Restelli, Francesco Falco, Jacopo Acerbi, Francesco Schiariti, Marco Paolo Ferroli, Paolo Broggi, Morgan Front Oncol Oncology BACKGROUND: Sporadic Spinal Psammomatous Malignant Melanotic Nerve Sheath Tumor (SSP-MMNST) is a rare subgroup of peripheral nerve sheath tumors arising along the spine. Only a few reports of SSP-MMNST have been described. In this paper, we review the literature on SSP-MMNST focusing on clinical, and diagnostic features, as well as investigating possible pathogenetic mechanisms to better implement therapeutic strategies. We also report an illustrative case of a young female presenting with cervicobrachial pain due to two SSP-MMNSTs arising from C5-6 right spinal roots. CASE DESCRIPTION: We report a case of a 28-year-old woman presenting with right arm weakness and dysesthesia. Clinical examination and neuroimaging were performed, and, following surgical removal of both lesions, a histological diagnosis of SSP-MMNST was obtained. RESULTS: The literature review identified 21 eligible studies assessing 23 patients with SSP-MMNST, with a mean onset age of 41 years and a slight male gender preference. The lumbar district was the most involved spinal segment. Gross-total resection (GTR) was the treatment of choice in all amenable cases, followed in selected cases with residual tumor by adjuvant radiotherapy or chemotherapy. The metastatic and recurrence rates were 31.58% and 36.8%, respectively. CONCLUSION: Differently from common schwannomas, MMNST represents a rare disease with known recurrence and metastatization propensity. As reported in our review, SSP-MMNST has a greater recurrence rate when compared to other forms of spinal MMNST, raising questions about the greater aggressiveness of the former. We also found that residual disease is related to a higher risk of systemic disease spreading. This metastatic potential, usually associated with primary lumbar localization, is characterized by a slight male prevalence. Indeed, whenever GTR is unachievable, considering the higher recurrence rate, adjuvant radiation therapy should be taken into consideration. Frontiers Media S.A. 2023-02-24 /pmc/articles/PMC9998981/ /pubmed/36910634 http://dx.doi.org/10.3389/fonc.2023.1100532 Text en Copyright © 2023 Bonomo, Gans, Mazzapicchi, Rubiu, Alimonti, Eoli, Paterra, Pollo, Iess, Restelli, Falco, Acerbi, Schiariti, Ferroli and Broggi https://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 Oncology
Bonomo, Giulio
Gans, Alessandro
Mazzapicchi, Elio
Rubiu, Emanuele
Alimonti, Paolo
Eoli, Marica
Paterra, Rosina
Pollo, Bianca
Iess, Guglielmo
Restelli, Francesco
Falco, Jacopo
Acerbi, Francesco
Schiariti, Marco Paolo
Ferroli, Paolo
Broggi, Morgan
Sporadic spinal psammomatous malignant melanotic nerve sheath tumor: A case report and literature review
title Sporadic spinal psammomatous malignant melanotic nerve sheath tumor: A case report and literature review
title_full Sporadic spinal psammomatous malignant melanotic nerve sheath tumor: A case report and literature review
title_fullStr Sporadic spinal psammomatous malignant melanotic nerve sheath tumor: A case report and literature review
title_full_unstemmed Sporadic spinal psammomatous malignant melanotic nerve sheath tumor: A case report and literature review
title_short Sporadic spinal psammomatous malignant melanotic nerve sheath tumor: A case report and literature review
title_sort sporadic spinal psammomatous malignant melanotic nerve sheath tumor: a case report and literature review
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998981/
https://www.ncbi.nlm.nih.gov/pubmed/36910634
http://dx.doi.org/10.3389/fonc.2023.1100532
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