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A case of mediastinal teratoma with malignant transformation into angiosarcoma and relapse with multiple bone metastases that was cured by a multidisciplinary treatment
INTRODUCTION: Complete resection is essential for the treatment of teratoma with malignant transformation, and if metastasis occurs, it will be difficult to cure. We report a case of primary mediastinal teratoma with differentiation into angiosarcoma that caused bone metastases but was cured by mult...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978083/ https://www.ncbi.nlm.nih.gov/pubmed/36874996 http://dx.doi.org/10.1002/iju5.12551 |
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author | Tani, Masaru Nagahara, Akira Takada, Shingo Fujita, Kazutoshi Fukuhara, Shinichiro Uemura, Motohide Kiuchi, Hiroshi Imamura, Ryoichi Nonomura, Norio |
author_facet | Tani, Masaru Nagahara, Akira Takada, Shingo Fujita, Kazutoshi Fukuhara, Shinichiro Uemura, Motohide Kiuchi, Hiroshi Imamura, Ryoichi Nonomura, Norio |
author_sort | Tani, Masaru |
collection | PubMed |
description | INTRODUCTION: Complete resection is essential for the treatment of teratoma with malignant transformation, and if metastasis occurs, it will be difficult to cure. We report a case of primary mediastinal teratoma with differentiation into angiosarcoma that caused bone metastases but was cured by multidisciplinary treatment. CASE PRESENTATION: A 31‐year‐old man with a primary mediastinal germ cell tumor underwent primary chemotherapy followed by post‐chemotherapy resection, with angiosarcoma due to malignant transformation found in the surgical specimen. Femoral diaphyseal metastasis was manifested, and he underwent femur curettage followed by radiation therapy of 60 Gy in parallel with 4 cycles of chemotherapy combining gemcitabine and docetaxel. Although thoracic vertebral bone metastasis emerged 5 months after treatment, intensity‐modulated radiation therapy was successful, and metastatic lesions have remained shrunken for 39 months after treatment. CONCLUSION: Even if complete resection is difficult, teratoma with malignant transformation may be cured by multidisciplinary treatment based on histopathology. |
format | Online Article Text |
id | pubmed-9978083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99780832023-03-03 A case of mediastinal teratoma with malignant transformation into angiosarcoma and relapse with multiple bone metastases that was cured by a multidisciplinary treatment Tani, Masaru Nagahara, Akira Takada, Shingo Fujita, Kazutoshi Fukuhara, Shinichiro Uemura, Motohide Kiuchi, Hiroshi Imamura, Ryoichi Nonomura, Norio IJU Case Rep Case Reports INTRODUCTION: Complete resection is essential for the treatment of teratoma with malignant transformation, and if metastasis occurs, it will be difficult to cure. We report a case of primary mediastinal teratoma with differentiation into angiosarcoma that caused bone metastases but was cured by multidisciplinary treatment. CASE PRESENTATION: A 31‐year‐old man with a primary mediastinal germ cell tumor underwent primary chemotherapy followed by post‐chemotherapy resection, with angiosarcoma due to malignant transformation found in the surgical specimen. Femoral diaphyseal metastasis was manifested, and he underwent femur curettage followed by radiation therapy of 60 Gy in parallel with 4 cycles of chemotherapy combining gemcitabine and docetaxel. Although thoracic vertebral bone metastasis emerged 5 months after treatment, intensity‐modulated radiation therapy was successful, and metastatic lesions have remained shrunken for 39 months after treatment. CONCLUSION: Even if complete resection is difficult, teratoma with malignant transformation may be cured by multidisciplinary treatment based on histopathology. John Wiley and Sons Inc. 2022-11-11 /pmc/articles/PMC9978083/ /pubmed/36874996 http://dx.doi.org/10.1002/iju5.12551 Text en © 2022 The Authors. IJU Case Reports published by John Wiley & Sons Australia, Ltd on behalf of Japanese Urological Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Tani, Masaru Nagahara, Akira Takada, Shingo Fujita, Kazutoshi Fukuhara, Shinichiro Uemura, Motohide Kiuchi, Hiroshi Imamura, Ryoichi Nonomura, Norio A case of mediastinal teratoma with malignant transformation into angiosarcoma and relapse with multiple bone metastases that was cured by a multidisciplinary treatment |
title | A case of mediastinal teratoma with malignant transformation into angiosarcoma and relapse with multiple bone metastases that was cured by a multidisciplinary treatment |
title_full | A case of mediastinal teratoma with malignant transformation into angiosarcoma and relapse with multiple bone metastases that was cured by a multidisciplinary treatment |
title_fullStr | A case of mediastinal teratoma with malignant transformation into angiosarcoma and relapse with multiple bone metastases that was cured by a multidisciplinary treatment |
title_full_unstemmed | A case of mediastinal teratoma with malignant transformation into angiosarcoma and relapse with multiple bone metastases that was cured by a multidisciplinary treatment |
title_short | A case of mediastinal teratoma with malignant transformation into angiosarcoma and relapse with multiple bone metastases that was cured by a multidisciplinary treatment |
title_sort | case of mediastinal teratoma with malignant transformation into angiosarcoma and relapse with multiple bone metastases that was cured by a multidisciplinary treatment |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978083/ https://www.ncbi.nlm.nih.gov/pubmed/36874996 http://dx.doi.org/10.1002/iju5.12551 |
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