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Bone disease in testicular and extragonadal germ cell tumours.
Of 297 patients with metastatic testicular and extragonadal germ cell tumours (GCT), bone involvement was detected clinically in 3% (7/251) of those at first presentation and in 9% (4/46) of relapsed cases. This difference was not statistically significant (95% confidence limits -2%; +14%). Concurre...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1988
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246879/ https://www.ncbi.nlm.nih.gov/pubmed/3224081 |
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author | Hitchins, R. N. Philip, P. A. Wignall, B. Newlands, E. S. Begent, R. H. Rustin, G. J. Bagshawe, K. D. |
author_facet | Hitchins, R. N. Philip, P. A. Wignall, B. Newlands, E. S. Begent, R. H. Rustin, G. J. Bagshawe, K. D. |
author_sort | Hitchins, R. N. |
collection | PubMed |
description | Of 297 patients with metastatic testicular and extragonadal germ cell tumours (GCT), bone involvement was detected clinically in 3% (7/251) of those at first presentation and in 9% (4/46) of relapsed cases. This difference was not statistically significant (95% confidence limits -2%; +14%). Concurrent systemic metastases, commonly involving lung (7/11 cases) and para-aortic lymph nodes (6/11), were present in all patients with bone disease. All affected patients had localized bone pain and lumbar spine was the most frequent site involved (9/11). Spinal cord compression occurred in two patients while a third developed progressive vertebral collapse after chemotherapy and required extensive surgical reconstruction. At median follow-up of 4 years, survival among patients presenting with bone disease (6/7) was similar to overall survival in the whole group (84%) and appeared better than in those with liver (18/26, 69%) or central nervous system (6/9) metastases at presentation. Back pain in metastatic germ cell tumours is often due to retroperitoneal lymphadenopathy but lumbar spine osseus metastases must be recognized early if severe potential complications, such as spinal cord compression, are to be avoided. In this series, bone metastases were not seen in the absence of widespread systemic disease suggesting all solitary bony lesions in GCT patients should be biopsied. IMAGES: |
format | Text |
id | pubmed-2246879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1988 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22468792009-09-10 Bone disease in testicular and extragonadal germ cell tumours. Hitchins, R. N. Philip, P. A. Wignall, B. Newlands, E. S. Begent, R. H. Rustin, G. J. Bagshawe, K. D. Br J Cancer Research Article Of 297 patients with metastatic testicular and extragonadal germ cell tumours (GCT), bone involvement was detected clinically in 3% (7/251) of those at first presentation and in 9% (4/46) of relapsed cases. This difference was not statistically significant (95% confidence limits -2%; +14%). Concurrent systemic metastases, commonly involving lung (7/11 cases) and para-aortic lymph nodes (6/11), were present in all patients with bone disease. All affected patients had localized bone pain and lumbar spine was the most frequent site involved (9/11). Spinal cord compression occurred in two patients while a third developed progressive vertebral collapse after chemotherapy and required extensive surgical reconstruction. At median follow-up of 4 years, survival among patients presenting with bone disease (6/7) was similar to overall survival in the whole group (84%) and appeared better than in those with liver (18/26, 69%) or central nervous system (6/9) metastases at presentation. Back pain in metastatic germ cell tumours is often due to retroperitoneal lymphadenopathy but lumbar spine osseus metastases must be recognized early if severe potential complications, such as spinal cord compression, are to be avoided. In this series, bone metastases were not seen in the absence of widespread systemic disease suggesting all solitary bony lesions in GCT patients should be biopsied. IMAGES: Nature Publishing Group 1988-12 /pmc/articles/PMC2246879/ /pubmed/3224081 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Hitchins, R. N. Philip, P. A. Wignall, B. Newlands, E. S. Begent, R. H. Rustin, G. J. Bagshawe, K. D. Bone disease in testicular and extragonadal germ cell tumours. |
title | Bone disease in testicular and extragonadal germ cell tumours. |
title_full | Bone disease in testicular and extragonadal germ cell tumours. |
title_fullStr | Bone disease in testicular and extragonadal germ cell tumours. |
title_full_unstemmed | Bone disease in testicular and extragonadal germ cell tumours. |
title_short | Bone disease in testicular and extragonadal germ cell tumours. |
title_sort | bone disease in testicular and extragonadal germ cell tumours. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246879/ https://www.ncbi.nlm.nih.gov/pubmed/3224081 |
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