A case of neurofibromatosis type 1 with neurofibromatosis type 1-related and neurofibromatosis type 1-unrelated tumors: a case report
Though rare, multiple neurofibromatosis type 1-unrelated tumors can develop in neurofibromatosis type 1 patients, which demands attention and interdisciplinary management. All related genes should be screened for potential pathogenic variants.
Authors
- Lan Kluwe (ORCID: https://orcid.org/0000-0001-9919-4551)
- Said Farschtschi (ORCID: https://orcid.org/0000-0002-3596-5932)
- Tabea I. Hartung
- Qais Karimi
Institutions
- Universität Hamburg (DE)
- University Medical Center Hamburg-Eppendorf (DE)
Publication Details
- Journal
- Journal of Medical Case Reports
- Published
- 2025-10-13
- DOI
- https://doi.org/10.1186/s13256-025-05599-z
- Primary Topic
- Neurofibromatosis and Schwannoma Cases
- Type
- article
- Field-Weighted Citation Impact
- 0.00