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Solitary fibrous tumour presenting with a single bone metastasis: report of six cases and literature review
BACKGROUND: Solitary fibrous tumour (SFT) is a rare soft tissue sarcoma with a low metastatic potential. A higher metastatic rate is observed in the high-grade/dedifferentiated variant. The most common expected site of distant spread are the lungs and the liver. Bone involvement is generally viewed...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007728/ https://www.ncbi.nlm.nih.gov/pubmed/27588167 http://dx.doi.org/10.1186/s13569-016-0055-1 |
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author | Colia, Vittoria Provenzano, Salvatore Morosi, Carlo Collini, Paola Renne, Salvatore Lorenzo Dagrada, Paolo G. Sangalli, Claudia Dei Tos, Angelo Paolo Marrari, Andrea Casali, Paolo G. Stacchiotti, Silvia |
author_facet | Colia, Vittoria Provenzano, Salvatore Morosi, Carlo Collini, Paola Renne, Salvatore Lorenzo Dagrada, Paolo G. Sangalli, Claudia Dei Tos, Angelo Paolo Marrari, Andrea Casali, Paolo G. Stacchiotti, Silvia |
author_sort | Colia, Vittoria |
collection | PubMed |
description | BACKGROUND: Solitary fibrous tumour (SFT) is a rare soft tissue sarcoma with a low metastatic potential. A higher metastatic rate is observed in the high-grade/dedifferentiated variant. The most common expected site of distant spread are the lungs and the liver. Bone involvement is generally viewed as a late stage of disease spread. We report on a retrospective series of SFT patients relapsing with a single distant bone recurrence as first metastatic event, without evidence of other organ involvement. CASE PRESENTATION: All patients affected by a single distant bone metastasis from SFT as first distant event, without any evidence of other site of metastasis, observed at our Institution, were considered. Bone involvement from SFT was pathologically assessed in all cases and confirmed by expert pathologists. A total of six patients were retrospectively identified. Primary tumour arose from the meninges in four patients, from soft tissues in two. Bone metastases were located to the vertebrae, the hip, the acetabulum and the rib. In all cases, bone relapse was the first event, with one patient presenting a local relapse. Median time from the primary tumour and the evidence of bone relapse was 40 months (range 0–58). In 2/6 patients bone metastasis was treated with radiotherapy (RT), in 2/6 with surgery, in 2/6 with surgery plus RT. At a median follow-up of 55 months (range 23–88), 5/6 patients are alive (2/5 without disease, 3/5 with multicentric metastatic disease) and one is dead of disease. 2/6 patients did not relapse after the treatment of the bone metastasis. CONCLUSIONS: This small series in a relatively rare histology suggests that isolated, possibly late, bone metastases are a plausible scenario, in particular in meningeal SFT. Notably, new bone lesions in a patient with a history of SFT should be always investigated. Exclusive local treatments may be an option, though collection of such series would be needed to define the best treatment strategy. |
format | Online Article Text |
id | pubmed-5007728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50077282016-09-02 Solitary fibrous tumour presenting with a single bone metastasis: report of six cases and literature review Colia, Vittoria Provenzano, Salvatore Morosi, Carlo Collini, Paola Renne, Salvatore Lorenzo Dagrada, Paolo G. Sangalli, Claudia Dei Tos, Angelo Paolo Marrari, Andrea Casali, Paolo G. Stacchiotti, Silvia Clin Sarcoma Res Case Report BACKGROUND: Solitary fibrous tumour (SFT) is a rare soft tissue sarcoma with a low metastatic potential. A higher metastatic rate is observed in the high-grade/dedifferentiated variant. The most common expected site of distant spread are the lungs and the liver. Bone involvement is generally viewed as a late stage of disease spread. We report on a retrospective series of SFT patients relapsing with a single distant bone recurrence as first metastatic event, without evidence of other organ involvement. CASE PRESENTATION: All patients affected by a single distant bone metastasis from SFT as first distant event, without any evidence of other site of metastasis, observed at our Institution, were considered. Bone involvement from SFT was pathologically assessed in all cases and confirmed by expert pathologists. A total of six patients were retrospectively identified. Primary tumour arose from the meninges in four patients, from soft tissues in two. Bone metastases were located to the vertebrae, the hip, the acetabulum and the rib. In all cases, bone relapse was the first event, with one patient presenting a local relapse. Median time from the primary tumour and the evidence of bone relapse was 40 months (range 0–58). In 2/6 patients bone metastasis was treated with radiotherapy (RT), in 2/6 with surgery, in 2/6 with surgery plus RT. At a median follow-up of 55 months (range 23–88), 5/6 patients are alive (2/5 without disease, 3/5 with multicentric metastatic disease) and one is dead of disease. 2/6 patients did not relapse after the treatment of the bone metastasis. CONCLUSIONS: This small series in a relatively rare histology suggests that isolated, possibly late, bone metastases are a plausible scenario, in particular in meningeal SFT. Notably, new bone lesions in a patient with a history of SFT should be always investigated. Exclusive local treatments may be an option, though collection of such series would be needed to define the best treatment strategy. BioMed Central 2016-09-01 /pmc/articles/PMC5007728/ /pubmed/27588167 http://dx.doi.org/10.1186/s13569-016-0055-1 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Colia, Vittoria Provenzano, Salvatore Morosi, Carlo Collini, Paola Renne, Salvatore Lorenzo Dagrada, Paolo G. Sangalli, Claudia Dei Tos, Angelo Paolo Marrari, Andrea Casali, Paolo G. Stacchiotti, Silvia Solitary fibrous tumour presenting with a single bone metastasis: report of six cases and literature review |
title | Solitary fibrous tumour presenting with a single bone metastasis: report of six cases and literature review |
title_full | Solitary fibrous tumour presenting with a single bone metastasis: report of six cases and literature review |
title_fullStr | Solitary fibrous tumour presenting with a single bone metastasis: report of six cases and literature review |
title_full_unstemmed | Solitary fibrous tumour presenting with a single bone metastasis: report of six cases and literature review |
title_short | Solitary fibrous tumour presenting with a single bone metastasis: report of six cases and literature review |
title_sort | solitary fibrous tumour presenting with a single bone metastasis: report of six cases and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007728/ https://www.ncbi.nlm.nih.gov/pubmed/27588167 http://dx.doi.org/10.1186/s13569-016-0055-1 |
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