Anaplastic Sarcoma of the Kidney in a Child with <i>DICER1</i> Syndrome: A Case Report
Treatment with intensive chemotherapy (vincristine, doxorubicin, etoposide, and cyclophosphamide) and abdominal irradiation was effective as 2-year event-free survival was achieved. Since <i>DICER1</i> syndrome causes a variety of rare cancers, particularly in infants and young adults, all surgeons and pediatric oncologists should be aware of the possibility of <i>DICER1</i> syndrome.
Authors
- Tsugumichi Koshinaga (ORCID: https://orcid.org/0000-0002-1396-2589)
- Shuichiro Uehara (ORCID: https://orcid.org/0000-0001-6542-3782)
- Eri Nagasaki‐Maeoka (ORCID: https://orcid.org/0000-0001-6413-3302)
- Yoshiko Nakano (ORCID: https://orcid.org/0000-0001-5394-8194)
- Hiroshi Yagasaki (ORCID: https://orcid.org/0000-0002-7937-5512)
- Motohiro Kato (ORCID: https://orcid.org/0000-0001-5145-1774)
- Ryusuke Tsujimura
- Katsuyoshi Shimozawa (ORCID: https://orcid.org/0000-0002-9285-4649)
- Haruna Nishimaki‐Watanabe
- Masaru Ueno (ORCID: https://orcid.org/0000-0002-9424-4609)
- Kanako Saiki
Institutions
- Nihon University (JP)
- Jichi Medical University (JP)
- Jichi Medical University Saitama Medical Center (JP)
- The University of Tokyo (JP)
Publication Details
- Journal
- Surgical Case Reports
- Published
- 2025-01-01
- DOI
- https://doi.org/10.70352/scrj.cr.25-0010
- Primary Topic
- Congenital Diaphragmatic Hernia Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Agency for Medical Research and Development