When the second comes first– rhabdomyosarcoma preceding heritable retinoblastoma– a case report
Abstract Background Retinoblastoma (rb) is the most frequent intraocular tumor, accounting for 3% of all childhood cancers. Heritable rb survivors are germline carriers for an RB1 mutation and have a lifelong risk to develop non-ocular second primary tumors (SPTs) involving multiple other organs lik...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BMC
2024-01-01
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| Cyfres: | BMC Ophthalmology |
| Pynciau: | |
| Mynediad Ar-lein: | https://doi.org/10.1186/s12886-024-03307-x |
| Tagiau: |
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