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Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor: A Case Report and Review of the Literature
Uterine leiomyosarcoma (uLMS) is a rare and aggressive malignancy with poor clinical outcomes. Even when localized, uLMS is associated with high rates of local and distant recurrences that are usually fatal. Common sites of recurrence are lung, liver, pelvic lymph nodes, and vertebral and long bones...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308452/ https://www.ncbi.nlm.nih.gov/pubmed/32612948 http://dx.doi.org/10.3389/fonc.2020.00869 |
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author | Rizzo, Alessandro Nigro, Maria Concetta Ramponi, Vania Gallo, Carmine Perrone, Anna Myriam De Iaco, Pierandrea Frezza, Giovanni Balestrini, Damiano Di Benedetto, Maika Morbiducci, Jarno Pantaleo, Maria Abbondanza Nannini, Margherita |
author_facet | Rizzo, Alessandro Nigro, Maria Concetta Ramponi, Vania Gallo, Carmine Perrone, Anna Myriam De Iaco, Pierandrea Frezza, Giovanni Balestrini, Damiano Di Benedetto, Maika Morbiducci, Jarno Pantaleo, Maria Abbondanza Nannini, Margherita |
author_sort | Rizzo, Alessandro |
collection | PubMed |
description | Uterine leiomyosarcoma (uLMS) is a rare and aggressive malignancy with poor clinical outcomes. Even when localized, uLMS is associated with high rates of local and distant recurrences that are usually fatal. Common sites of recurrence are lung, liver, pelvic lymph nodes, and vertebral and long bones, though atypical patterns of recurrence have been described. Among them, intracranial recurrence appears as a rare finding, almost exceptional in skull and dura. We describe the case of a solitary skull metastasis from uLMS in a 39-year-old woman, which represents the third reported case of skull recurrence in literature. After multidisciplinary discussion, the patient underwent surgery and received adjuvant radiotherapy. After 4 months, she is currently alive, without evidence of extracranial disease. This case highlights the importance of suspecting and recognizing atypical and extremely rare metastasis to this region. We encourage the need for large case series in order to provide further information about cranial recurrences of uLMS taking into account the paucity of data currently available in literature and the frequently unpredictable behavior of this rare and highly lethal disease. |
format | Online Article Text |
id | pubmed-7308452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73084522020-06-30 Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor: A Case Report and Review of the Literature Rizzo, Alessandro Nigro, Maria Concetta Ramponi, Vania Gallo, Carmine Perrone, Anna Myriam De Iaco, Pierandrea Frezza, Giovanni Balestrini, Damiano Di Benedetto, Maika Morbiducci, Jarno Pantaleo, Maria Abbondanza Nannini, Margherita Front Oncol Oncology Uterine leiomyosarcoma (uLMS) is a rare and aggressive malignancy with poor clinical outcomes. Even when localized, uLMS is associated with high rates of local and distant recurrences that are usually fatal. Common sites of recurrence are lung, liver, pelvic lymph nodes, and vertebral and long bones, though atypical patterns of recurrence have been described. Among them, intracranial recurrence appears as a rare finding, almost exceptional in skull and dura. We describe the case of a solitary skull metastasis from uLMS in a 39-year-old woman, which represents the third reported case of skull recurrence in literature. After multidisciplinary discussion, the patient underwent surgery and received adjuvant radiotherapy. After 4 months, she is currently alive, without evidence of extracranial disease. This case highlights the importance of suspecting and recognizing atypical and extremely rare metastasis to this region. We encourage the need for large case series in order to provide further information about cranial recurrences of uLMS taking into account the paucity of data currently available in literature and the frequently unpredictable behavior of this rare and highly lethal disease. Frontiers Media S.A. 2020-06-16 /pmc/articles/PMC7308452/ /pubmed/32612948 http://dx.doi.org/10.3389/fonc.2020.00869 Text en Copyright © 2020 Rizzo, Nigro, Ramponi, Gallo, Perrone, De Iaco, Frezza, Balestrini, Di Benedetto, Morbiducci, Pantaleo and Nannini. 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 | Oncology Rizzo, Alessandro Nigro, Maria Concetta Ramponi, Vania Gallo, Carmine Perrone, Anna Myriam De Iaco, Pierandrea Frezza, Giovanni Balestrini, Damiano Di Benedetto, Maika Morbiducci, Jarno Pantaleo, Maria Abbondanza Nannini, Margherita Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor: A Case Report and Review of the Literature |
title | Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor: A Case Report and Review of the Literature |
title_full | Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor: A Case Report and Review of the Literature |
title_fullStr | Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor: A Case Report and Review of the Literature |
title_full_unstemmed | Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor: A Case Report and Review of the Literature |
title_short | Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor: A Case Report and Review of the Literature |
title_sort | skull metastasis from uterine leiomyosarcoma, a rare presentation for a rare tumor: a case report and review of the literature |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308452/ https://www.ncbi.nlm.nih.gov/pubmed/32612948 http://dx.doi.org/10.3389/fonc.2020.00869 |
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