Oral Squamous Cell Carcinoma in a Patient with Fanconi Anemia




Huuhka Milla, Turunen Aaro

PublisherHINDAWI LTD

2021

Case Reports in Dentistry

CASE REPORTS IN DENTISTRY

CASE REP DENT

ARTN 5571649

2021

4

2090-6447

DOIhttps://doi.org/10.1155/2021/5571649

https://research.utu.fi/converis/portal/detail/Publication/66662508



Fanconi anemia (FA) is a rare autosomal recessive genetic disorder characterized by different types of malformations, skin lesions, bone marrow failure, and increased risk for both hematological malignancies and solid tumors, especially head and neck squamous cell carcinomas (HNSCC). FA patients may also display a low tolerance to oncologic treatments. The authors present a case of mandibular squamous cell carcinoma in a young FA patient. Because of the aggressive nature of the SCC and complex treatment options, we recommend a strict lifelong follow-up for all FA patients to detect early changes in the oral mucosa.

Last updated on 2024-26-11 at 23:30