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.

Gasparini, G., Longobardi, G., Boniello, R., Di Petrillo, A., Pelo, S., Fanconi anemia manifesting as a squamous cell carcinoma of the hard palate: A case report, <<HEAD & FACE MEDICINE>>, 2006; 2 (1): 1-N/A. [doi:10.1186/1746-160X-2-1] [http://hdl.handle.net/10807/154168]

Fanconi anemia manifesting as a squamous cell carcinoma of the hard palate: A case report

Gasparini, Giulio;Longobardi, Gianluigi;Boniello, Roberto;Pelo, Sandro
2006

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.
2006
Inglese
Gasparini, G., Longobardi, G., Boniello, R., Di Petrillo, A., Pelo, S., Fanconi anemia manifesting as a squamous cell carcinoma of the hard palate: A case report, <<HEAD & FACE MEDICINE>>, 2006; 2 (1): 1-N/A. [doi:10.1186/1746-160X-2-1] [http://hdl.handle.net/10807/154168]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/154168
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