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Surgical Treatment for Skeletal Metastases From Soft Tissue Sarcomas: Experience With 23 Lesions in 20 Patients

Purpose. This paper reports the procedures and the clinical results of a series of surgical treatments for skeletal metastases from soft tissue sarcomas. Subjects and methods. Surgical treatment of metastatic bony lesions from soft tissue sarcomas has been carried out over a 20 year period (1975–199...

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Autores principales: Yoshikawa, Hideki, Ueda, Takafumi, Kudawara, Ikuo, Araki, Nobuhito, Yonenobu, Kazuo, Ochi, Takahiro, Uchida, Atsumasa
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395386/
https://www.ncbi.nlm.nih.gov/pubmed/18521241
http://dx.doi.org/10.1080/13577149878064
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author Yoshikawa, Hideki
Ueda, Takafumi
Kudawara, Ikuo
Araki, Nobuhito
Yonenobu, Kazuo
Ochi, Takahiro
Uchida, Atsumasa
author_facet Yoshikawa, Hideki
Ueda, Takafumi
Kudawara, Ikuo
Araki, Nobuhito
Yonenobu, Kazuo
Ochi, Takahiro
Uchida, Atsumasa
author_sort Yoshikawa, Hideki
collection PubMed
description Purpose. This paper reports the procedures and the clinical results of a series of surgical treatments for skeletal metastases from soft tissue sarcomas. Subjects and methods. Surgical treatment of metastatic bony lesions from soft tissue sarcomas has been carried out over a 20 year period (1975–1996). Thirty-two patients developed skeletal metastases from soft tissue sarcomas, and 20 of these cases received surgical treatment. The 23 metastatic bony lesions in these 20 patients were treated using the following surgical approaches: wide resection with prosthetic replacement in five lesions, wide or marginal resection without reconstruction in four lesions, intramedullarly nailing with curettage and methylmethacrylate cementation in four lesions, marginal resection of vertebral body with replacement by a ceramic prosthesis in three lesions, laminectomy in three lesions, intramedullarly nailing in two lesions, and curettage in two lesions. Results. Relief of pain was achieved in 17 of the 20 patients. The ambulatory status of the patients with metastasis in the lower extremity or periacetabular region was significantly improved in nine of 10 cases. Seventeen patients died of disease, with a mean survival period of 17.9 months after surgery for metastasis. Discussion. Although surgical treatment for skeletal metastases from soft tissue sarcomas cannot save the life of the patient, it can be of value in improving their well-being and overall quality of life. In these cases, surgical intervention may be more frequently indicated than in tumors with an osteoblastic or mixed pattern.
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spelling pubmed-23953862008-06-02 Surgical Treatment for Skeletal Metastases From Soft Tissue Sarcomas: Experience With 23 Lesions in 20 Patients Yoshikawa, Hideki Ueda, Takafumi Kudawara, Ikuo Araki, Nobuhito Yonenobu, Kazuo Ochi, Takahiro Uchida, Atsumasa Sarcoma Research Article Purpose. This paper reports the procedures and the clinical results of a series of surgical treatments for skeletal metastases from soft tissue sarcomas. Subjects and methods. Surgical treatment of metastatic bony lesions from soft tissue sarcomas has been carried out over a 20 year period (1975–1996). Thirty-two patients developed skeletal metastases from soft tissue sarcomas, and 20 of these cases received surgical treatment. The 23 metastatic bony lesions in these 20 patients were treated using the following surgical approaches: wide resection with prosthetic replacement in five lesions, wide or marginal resection without reconstruction in four lesions, intramedullarly nailing with curettage and methylmethacrylate cementation in four lesions, marginal resection of vertebral body with replacement by a ceramic prosthesis in three lesions, laminectomy in three lesions, intramedullarly nailing in two lesions, and curettage in two lesions. Results. Relief of pain was achieved in 17 of the 20 patients. The ambulatory status of the patients with metastasis in the lower extremity or periacetabular region was significantly improved in nine of 10 cases. Seventeen patients died of disease, with a mean survival period of 17.9 months after surgery for metastasis. Discussion. Although surgical treatment for skeletal metastases from soft tissue sarcomas cannot save the life of the patient, it can be of value in improving their well-being and overall quality of life. In these cases, surgical intervention may be more frequently indicated than in tumors with an osteoblastic or mixed pattern. Hindawi Publishing Corporation 1998-06 /pmc/articles/PMC2395386/ /pubmed/18521241 http://dx.doi.org/10.1080/13577149878064 Text en Copyright © 1998 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yoshikawa, Hideki
Ueda, Takafumi
Kudawara, Ikuo
Araki, Nobuhito
Yonenobu, Kazuo
Ochi, Takahiro
Uchida, Atsumasa
Surgical Treatment for Skeletal Metastases From Soft Tissue Sarcomas: Experience With 23 Lesions in 20 Patients
title Surgical Treatment for Skeletal Metastases From Soft Tissue Sarcomas: Experience With 23 Lesions in 20 Patients
title_full Surgical Treatment for Skeletal Metastases From Soft Tissue Sarcomas: Experience With 23 Lesions in 20 Patients
title_fullStr Surgical Treatment for Skeletal Metastases From Soft Tissue Sarcomas: Experience With 23 Lesions in 20 Patients
title_full_unstemmed Surgical Treatment for Skeletal Metastases From Soft Tissue Sarcomas: Experience With 23 Lesions in 20 Patients
title_short Surgical Treatment for Skeletal Metastases From Soft Tissue Sarcomas: Experience With 23 Lesions in 20 Patients
title_sort surgical treatment for skeletal metastases from soft tissue sarcomas: experience with 23 lesions in 20 patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395386/
https://www.ncbi.nlm.nih.gov/pubmed/18521241
http://dx.doi.org/10.1080/13577149878064
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