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

Author:

Gasparini Giulio,Longobardi Gianluigi,Boniello Roberto,Di Petrillo Alessandro,Pelo Sandro

Abstract

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.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,General Dentistry,Otorhinolaryngology

Reference18 articles.

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3. Swift MR, Hirschhorn K: Fanconi's anemia. inherited susceptibility to chromosome breakage in various tissue. Ann Intern Med. 1966, 65: 496-503.

4. Esparza A, Thompson WK: Familial hypoplastic anemia with multiple congenital anomalies (Fanconi's syndrome) – report of three cases. Cases presented are of two sisters and a female cousin with complete clinical and post mortem findings. R I Med J. 1966, 49: 103-110.

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