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Recurrence of Giant Cell Tumor of the Spine after Resection: A Report of 10 Cases
OBJECTIVE: To review the clinical details and further treatments for recurrent spinal giant cell tumors (SGCT), and to analyze the risk factors of recurrence and shed new light on the treatment options and prognosis of recurrent SGCT. METHODS: A retrospective analysis of recurrent SGCT between April...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001436/ https://www.ncbi.nlm.nih.gov/pubmed/29878714 http://dx.doi.org/10.1111/os.12375 |
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author | Lin, Peng Lin, Nong Teng, Wangsiyuan Wang, Sheng‐dong Pan, Wei‐bo Huang, Xin Yan, Xiao‐bo Liu, Meng Li, Heng‐yuan Li, Bing‐hao Sun, Ling‐ling Wang, Zhan Zhou, Xing‐zhi Ye, Zhao‐ming |
author_facet | Lin, Peng Lin, Nong Teng, Wangsiyuan Wang, Sheng‐dong Pan, Wei‐bo Huang, Xin Yan, Xiao‐bo Liu, Meng Li, Heng‐yuan Li, Bing‐hao Sun, Ling‐ling Wang, Zhan Zhou, Xing‐zhi Ye, Zhao‐ming |
author_sort | Lin, Peng |
collection | PubMed |
description | OBJECTIVE: To review the clinical details and further treatments for recurrent spinal giant cell tumors (SGCT), and to analyze the risk factors of recurrence and shed new light on the treatment options and prognosis of recurrent SGCT. METHODS: A retrospective analysis of recurrent SGCT between April 2003 and January 2014 was performed. A total of 10 patients comprising 3 men and 7 women with a mean age of 28.9 years (range, 21–40 years) were included in the study. All complete clinical data, radiographs, CT, MRI, scans and pathological data were reviewed. The tumor locations and the regions involved were evaluated by CT and MRI. The blood supply of the tumors was evaluated by enhanced CT and MRI. The mean follow‐up was 81.3 months (range, 35.7–172.1 months). RESULTS: All patients had Enneking stage 3 tumors; 9 (90%) of them had different extents of spinal canal involvement in the primary time period. All patients underwent intralesional resection during their first surgery. Only 1 patient received local adjuvant treatments; no patient underwent selective arterial embolization or used denosumab at that time. Only 1 patient underwent adjuvant radiotherapy postoperatively, and another patient used bisphosphonates. After recurrence, 1 patient was cured using denosumab, and 2 patients' disease was controlled through use of other medical treatments or adjuvant treatments. There were 3 repeated recurrences and 7 repeated surgical procedures were performed in 5 patients. There were 6 intralesional excisions and 1 decompression surgery. The mean relapse‐free time after the first surgery was 32.3 months (range, 10.5–62.6 months). The overall mean relapse‐free time was 40.2 months (range, 10.5–157 months). No distant metastasis was found in our series. At the final follow‐up, 4 patients were disease free, 3 patients' disease was under control, 2 has progressive disease aggravation, while 1 patient died as a result of progression of disease 133.9 months after first surgery. CONCLUSION: Intralesional excision for recurrent spinal giant cell tumors is an effective option that may have satisfactory prognosis. However, the excision and the inactivation of the lesion should be carried out carefully and thoroughly without missing any corners. Early diagnosis of recurrence may be associated with better prognosis. Adjuvant treatments perioperatively and systemic medical treatments can decrease recurrence rates and can have therapeutic effects in the recurrent SGCT. |
format | Online Article Text |
id | pubmed-6001436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60014362018-06-21 Recurrence of Giant Cell Tumor of the Spine after Resection: A Report of 10 Cases Lin, Peng Lin, Nong Teng, Wangsiyuan Wang, Sheng‐dong Pan, Wei‐bo Huang, Xin Yan, Xiao‐bo Liu, Meng Li, Heng‐yuan Li, Bing‐hao Sun, Ling‐ling Wang, Zhan Zhou, Xing‐zhi Ye, Zhao‐ming Orthop Surg Clinical Articles OBJECTIVE: To review the clinical details and further treatments for recurrent spinal giant cell tumors (SGCT), and to analyze the risk factors of recurrence and shed new light on the treatment options and prognosis of recurrent SGCT. METHODS: A retrospective analysis of recurrent SGCT between April 2003 and January 2014 was performed. A total of 10 patients comprising 3 men and 7 women with a mean age of 28.9 years (range, 21–40 years) were included in the study. All complete clinical data, radiographs, CT, MRI, scans and pathological data were reviewed. The tumor locations and the regions involved were evaluated by CT and MRI. The blood supply of the tumors was evaluated by enhanced CT and MRI. The mean follow‐up was 81.3 months (range, 35.7–172.1 months). RESULTS: All patients had Enneking stage 3 tumors; 9 (90%) of them had different extents of spinal canal involvement in the primary time period. All patients underwent intralesional resection during their first surgery. Only 1 patient received local adjuvant treatments; no patient underwent selective arterial embolization or used denosumab at that time. Only 1 patient underwent adjuvant radiotherapy postoperatively, and another patient used bisphosphonates. After recurrence, 1 patient was cured using denosumab, and 2 patients' disease was controlled through use of other medical treatments or adjuvant treatments. There were 3 repeated recurrences and 7 repeated surgical procedures were performed in 5 patients. There were 6 intralesional excisions and 1 decompression surgery. The mean relapse‐free time after the first surgery was 32.3 months (range, 10.5–62.6 months). The overall mean relapse‐free time was 40.2 months (range, 10.5–157 months). No distant metastasis was found in our series. At the final follow‐up, 4 patients were disease free, 3 patients' disease was under control, 2 has progressive disease aggravation, while 1 patient died as a result of progression of disease 133.9 months after first surgery. CONCLUSION: Intralesional excision for recurrent spinal giant cell tumors is an effective option that may have satisfactory prognosis. However, the excision and the inactivation of the lesion should be carried out carefully and thoroughly without missing any corners. Early diagnosis of recurrence may be associated with better prognosis. Adjuvant treatments perioperatively and systemic medical treatments can decrease recurrence rates and can have therapeutic effects in the recurrent SGCT. John Wiley & Sons Australia, Ltd 2018-05-27 /pmc/articles/PMC6001436/ /pubmed/29878714 http://dx.doi.org/10.1111/os.12375 Text en © 2018 The Authors Orthopaedic Surgery published by Chinese Orthopaedic Association and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Clinical Articles Lin, Peng Lin, Nong Teng, Wangsiyuan Wang, Sheng‐dong Pan, Wei‐bo Huang, Xin Yan, Xiao‐bo Liu, Meng Li, Heng‐yuan Li, Bing‐hao Sun, Ling‐ling Wang, Zhan Zhou, Xing‐zhi Ye, Zhao‐ming Recurrence of Giant Cell Tumor of the Spine after Resection: A Report of 10 Cases |
title | Recurrence of Giant Cell Tumor of the Spine after Resection: A Report of 10 Cases |
title_full | Recurrence of Giant Cell Tumor of the Spine after Resection: A Report of 10 Cases |
title_fullStr | Recurrence of Giant Cell Tumor of the Spine after Resection: A Report of 10 Cases |
title_full_unstemmed | Recurrence of Giant Cell Tumor of the Spine after Resection: A Report of 10 Cases |
title_short | Recurrence of Giant Cell Tumor of the Spine after Resection: A Report of 10 Cases |
title_sort | recurrence of giant cell tumor of the spine after resection: a report of 10 cases |
topic | Clinical Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001436/ https://www.ncbi.nlm.nih.gov/pubmed/29878714 http://dx.doi.org/10.1111/os.12375 |
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