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Successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report
BACKGROUND: Desmoid-type fibromatosis is a rare disease that can result in hydronephrosis. Hydronephrosis associated with desmoid-type fibromatosis often requires surgery or ureteral stent insertion. Although radiation therapy is recommended for inoperable cases of desmoid-type fibromatosis, there h...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549302/ https://www.ncbi.nlm.nih.gov/pubmed/34702352 http://dx.doi.org/10.1186/s13256-021-03088-7 |
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author | Ishikawa, Yojiro Umezawa, Rei Yamamoto, Takaya Takahashi, Noriyoshi Takeda, Kazuya Suzuki, Yu Jingu, Keiichi |
author_facet | Ishikawa, Yojiro Umezawa, Rei Yamamoto, Takaya Takahashi, Noriyoshi Takeda, Kazuya Suzuki, Yu Jingu, Keiichi |
author_sort | Ishikawa, Yojiro |
collection | PubMed |
description | BACKGROUND: Desmoid-type fibromatosis is a rare disease that can result in hydronephrosis. Hydronephrosis associated with desmoid-type fibromatosis often requires surgery or ureteral stent insertion. Although radiation therapy is recommended for inoperable cases of desmoid-type fibromatosis, there has been no report of treatment for hydronephrosis associated with desmoid-type fibromatosis by radiation therapy alone. We herein report a case of successful treatment for inoperable recurrence of desmoid-type fibromatosis with unilateral hydronephrosis by radiation therapy alone. CASE PRESENTATION: A 43-year-old Japanese female underwent resection of desmoid-type fibromatosis in the right inguinal region and combined resection of the right external iliac vein 5 years before. Other treatment was not performed because of her pregnancy. Four years after surgery, desmoid-type fibromatosis recurred in the right pelvic wall. Cyclooxygenase-2 selective inhibitor treatment was given for 1 year, but her desmoid-type fibromatosis enlarged to more than 10 cm, and she had swelling of her right leg and hydronephrosis of her right kidney. The patient received 50.4 Gy in 28 fractions of prophylactic irradiation using 10 MV X-ray and 9 Gy in five fractions of a sequential boost for the recurrent desmoid-type fibromatosis. Although there was temporary tumor progression at 1 month after radiation therapy, slow regression of the tumor was seen. At 5 years after radiation therapy, there was no disease progression or severe complications. CONCLUSION: We experienced successful treatment for an inoperable case of desmoid-type fibromatosis with hydronephrosis. Moderate-dose radiation therapy alone is an effective and feasible approach for the management of hydronephrosis associated with desmoid-type fibromatosis. |
format | Online Article Text |
id | pubmed-8549302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85493022021-10-27 Successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report Ishikawa, Yojiro Umezawa, Rei Yamamoto, Takaya Takahashi, Noriyoshi Takeda, Kazuya Suzuki, Yu Jingu, Keiichi J Med Case Rep Case Report BACKGROUND: Desmoid-type fibromatosis is a rare disease that can result in hydronephrosis. Hydronephrosis associated with desmoid-type fibromatosis often requires surgery or ureteral stent insertion. Although radiation therapy is recommended for inoperable cases of desmoid-type fibromatosis, there has been no report of treatment for hydronephrosis associated with desmoid-type fibromatosis by radiation therapy alone. We herein report a case of successful treatment for inoperable recurrence of desmoid-type fibromatosis with unilateral hydronephrosis by radiation therapy alone. CASE PRESENTATION: A 43-year-old Japanese female underwent resection of desmoid-type fibromatosis in the right inguinal region and combined resection of the right external iliac vein 5 years before. Other treatment was not performed because of her pregnancy. Four years after surgery, desmoid-type fibromatosis recurred in the right pelvic wall. Cyclooxygenase-2 selective inhibitor treatment was given for 1 year, but her desmoid-type fibromatosis enlarged to more than 10 cm, and she had swelling of her right leg and hydronephrosis of her right kidney. The patient received 50.4 Gy in 28 fractions of prophylactic irradiation using 10 MV X-ray and 9 Gy in five fractions of a sequential boost for the recurrent desmoid-type fibromatosis. Although there was temporary tumor progression at 1 month after radiation therapy, slow regression of the tumor was seen. At 5 years after radiation therapy, there was no disease progression or severe complications. CONCLUSION: We experienced successful treatment for an inoperable case of desmoid-type fibromatosis with hydronephrosis. Moderate-dose radiation therapy alone is an effective and feasible approach for the management of hydronephrosis associated with desmoid-type fibromatosis. BioMed Central 2021-10-27 /pmc/articles/PMC8549302/ /pubmed/34702352 http://dx.doi.org/10.1186/s13256-021-03088-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Ishikawa, Yojiro Umezawa, Rei Yamamoto, Takaya Takahashi, Noriyoshi Takeda, Kazuya Suzuki, Yu Jingu, Keiichi Successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report |
title | Successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report |
title_full | Successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report |
title_fullStr | Successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report |
title_full_unstemmed | Successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report |
title_short | Successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report |
title_sort | successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549302/ https://www.ncbi.nlm.nih.gov/pubmed/34702352 http://dx.doi.org/10.1186/s13256-021-03088-7 |
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