DICER1 mutational analysis of pleuropulmonary blastoma: a single institutional experience
A high prevalence of DICER1 germline variants was observed in patients with PPB, consistent with previous studies. Family history alone may be insufficient to suspect DICER1 syndrome, and thus, proactive genetic testing of family members is advisable in all cases of PPB.
Authors
- Noriaki Sakamoto (ORCID: https://orcid.org/0000-0001-6573-6463)
- Sho Hosaka (ORCID: https://orcid.org/0000-0002-2792-1235)
- Keisuke Kato (ORCID: https://orcid.org/0000-0002-0135-5431)
- Masako Inaba
- Hiroko Fukushima (ORCID: https://orcid.org/0000-0002-1290-3501)
- Yuni Yamaki (ORCID: https://orcid.org/0000-0003-4287-5713)
- Kumie Nagatomo (ORCID: https://orcid.org/0000-0002-7286-054X)
- Hidetoshi Takada (ORCID: https://orcid.org/0000-0002-0741-5060)
- Ryoko Suzuki
Institutions
- University of Tsukuba (JP)
- University of Tsukuba Hospital (JP)
- Ibaraki Children's Hospital (JP)
Publication Details
- Journal
- Japanese Journal of Clinical Oncology
- Published
- 2025-11-02
- DOI
- https://doi.org/10.1093/jjco/hyaf180
- Citations
- 1
- Primary Topic
- Congenital Diaphragmatic Hernia Studies
- Type
- article
- Field-Weighted Citation Impact
- 2.01