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Giant cell tumor of the clavicle: report of a case in a rare location with consideration of surgical method
BACKGROUND: Most bone tumors that occur in the clavicle are malignant. A few giant cell tumors (GCTs) of the clavicle have been reported; however, the most appropriate operative method for this tumor has never been discussed. CASE PRESENTATION: A 54-year-old man noticed enlargement of the proximal a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464228/ https://www.ncbi.nlm.nih.gov/pubmed/26062917 http://dx.doi.org/10.1186/s12891-015-0604-4 |
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author | Nagano, Satoshi Tsuchimochi, Toru Yokouchi, Masahiro Setoguchi, Takao Sasaki, Hiromi Shimada, Hirofumi Nakamura, Shunsuke Ishidou, Yasuhiro Yamamoto, Takuya Komiya, Setsuro |
author_facet | Nagano, Satoshi Tsuchimochi, Toru Yokouchi, Masahiro Setoguchi, Takao Sasaki, Hiromi Shimada, Hirofumi Nakamura, Shunsuke Ishidou, Yasuhiro Yamamoto, Takuya Komiya, Setsuro |
author_sort | Nagano, Satoshi |
collection | PubMed |
description | BACKGROUND: Most bone tumors that occur in the clavicle are malignant. A few giant cell tumors (GCTs) of the clavicle have been reported; however, the most appropriate operative method for this tumor has never been discussed. CASE PRESENTATION: A 54-year-old man noticed enlargement of the proximal aspect of the right clavicle. A plain X-ray revealed lytic change and ballooning of the proximal end of the right clavicle. The tumor was isointense on T1-weighted magnetic resonance images and showed a mixture of low- and high-intensity areas on T2-weighted images without extension to the surrounding soft tissues. Bone scintigraphy showed strong accumulation (normal/tumor ratio, 2.31), and positron emission tomography revealed strong uptake of fluorine-18-2-fluoro-2-deoxy-d-glucose (SUVmax, 6.0) in the proximal part of the right clavicle. Because we could not completely exclude malignancy, an open biopsy was performed. Pathologically, the tumor comprised mononuclear stromal cells and multinuclear giant cells, resulting in a diagnosis of a GCT of the bone. Although curettage may be considered for such lesions (Campanacci grade II), we chose resection to minimize the chance of recurrence. The tumor was resected en-bloc with the proximal half of the clavicle. No postoperative shoulder disproportion was observed, and full range of motion of the right shoulder was maintained. The patient was satisfied with the surgical outcome (Musculoskeletal Tumor Society score of 96 %). He returned to his original job as a land and house investigator without any signs of recurrence for 1 year after surgery. CONCLUSIONS: Although GCT of the bone rarely occurs in the clavicle, the typical X-ray findings demonstrated in the present case are helpful for a correct diagnosis. Although en-bloc resection without reconstruction is appropriate for GCTs in expendable bones, there has been much discussion about shoulder function after total claviculectomy. Considering the importance of the function of the clavicle, which is to support the scapula through the acromioclavicular joint, we preserved the muscle attachments of the deltoid, trapezius, and pectoralis major. Because both the oncological and functional outcomes were satisfactory, we recommend preservation of as much of the clavicle as possible in patients with clavicular bone tumors. |
format | Online Article Text |
id | pubmed-4464228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44642282015-06-14 Giant cell tumor of the clavicle: report of a case in a rare location with consideration of surgical method Nagano, Satoshi Tsuchimochi, Toru Yokouchi, Masahiro Setoguchi, Takao Sasaki, Hiromi Shimada, Hirofumi Nakamura, Shunsuke Ishidou, Yasuhiro Yamamoto, Takuya Komiya, Setsuro BMC Musculoskelet Disord Case Report BACKGROUND: Most bone tumors that occur in the clavicle are malignant. A few giant cell tumors (GCTs) of the clavicle have been reported; however, the most appropriate operative method for this tumor has never been discussed. CASE PRESENTATION: A 54-year-old man noticed enlargement of the proximal aspect of the right clavicle. A plain X-ray revealed lytic change and ballooning of the proximal end of the right clavicle. The tumor was isointense on T1-weighted magnetic resonance images and showed a mixture of low- and high-intensity areas on T2-weighted images without extension to the surrounding soft tissues. Bone scintigraphy showed strong accumulation (normal/tumor ratio, 2.31), and positron emission tomography revealed strong uptake of fluorine-18-2-fluoro-2-deoxy-d-glucose (SUVmax, 6.0) in the proximal part of the right clavicle. Because we could not completely exclude malignancy, an open biopsy was performed. Pathologically, the tumor comprised mononuclear stromal cells and multinuclear giant cells, resulting in a diagnosis of a GCT of the bone. Although curettage may be considered for such lesions (Campanacci grade II), we chose resection to minimize the chance of recurrence. The tumor was resected en-bloc with the proximal half of the clavicle. No postoperative shoulder disproportion was observed, and full range of motion of the right shoulder was maintained. The patient was satisfied with the surgical outcome (Musculoskeletal Tumor Society score of 96 %). He returned to his original job as a land and house investigator without any signs of recurrence for 1 year after surgery. CONCLUSIONS: Although GCT of the bone rarely occurs in the clavicle, the typical X-ray findings demonstrated in the present case are helpful for a correct diagnosis. Although en-bloc resection without reconstruction is appropriate for GCTs in expendable bones, there has been much discussion about shoulder function after total claviculectomy. Considering the importance of the function of the clavicle, which is to support the scapula through the acromioclavicular joint, we preserved the muscle attachments of the deltoid, trapezius, and pectoralis major. Because both the oncological and functional outcomes were satisfactory, we recommend preservation of as much of the clavicle as possible in patients with clavicular bone tumors. BioMed Central 2015-06-12 /pmc/articles/PMC4464228/ /pubmed/26062917 http://dx.doi.org/10.1186/s12891-015-0604-4 Text en © Nagano et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Nagano, Satoshi Tsuchimochi, Toru Yokouchi, Masahiro Setoguchi, Takao Sasaki, Hiromi Shimada, Hirofumi Nakamura, Shunsuke Ishidou, Yasuhiro Yamamoto, Takuya Komiya, Setsuro Giant cell tumor of the clavicle: report of a case in a rare location with consideration of surgical method |
title | Giant cell tumor of the clavicle: report of a case in a rare location with consideration of surgical method |
title_full | Giant cell tumor of the clavicle: report of a case in a rare location with consideration of surgical method |
title_fullStr | Giant cell tumor of the clavicle: report of a case in a rare location with consideration of surgical method |
title_full_unstemmed | Giant cell tumor of the clavicle: report of a case in a rare location with consideration of surgical method |
title_short | Giant cell tumor of the clavicle: report of a case in a rare location with consideration of surgical method |
title_sort | giant cell tumor of the clavicle: report of a case in a rare location with consideration of surgical method |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464228/ https://www.ncbi.nlm.nih.gov/pubmed/26062917 http://dx.doi.org/10.1186/s12891-015-0604-4 |
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