Abstract
Fanconi Anemia is a rare autosomal recessive disorder characterized by various congenital malformations, progressive bone marrow failure at a very young age and of solid tumors development. The authors present a rare case of a squamous cell carcinoma of the hard palate in a Fanconi Anaemia patient. The atypical clinical manifestation rendered the diagnosis more difficult. This case, for age of appearance, sex and localization, is unique in international literature. We recommend a quarterly follow up of the oral-rhino-pharynx complex in FA patients and to consider as carcinomas, all oral lesions that last more than two weeks.
Lingua originale | English |
---|---|
pagine (da-a) | 1-N/A |
Rivista | HEAD & FACE MEDICINE |
Volume | 2 |
DOI | |
Stato di pubblicazione | Pubblicato - 2006 |
Keywords
- Adult
- Biopsy
- Carcinoma, Squamous Cell
- Diagnosis, Differential
- Fanconi Anemia
- Follow-Up Studies
- Humans
- Male
- Oral Surgical Procedures
- Palatal Neoplasms
- Palate, Hard
- Tomography, X-Ray Computed