Title of article :
Desmoplastic Fibroma Recurrence Associated with Tuberous Sclerosis in a Young Patient
Author/Authors :
Espinoza-Coronado, A. M. Faculty of Dentistry of San Luis Potosi - Universidad Autonoma de San Luis Potosı, San Luis Potosi, SLP, Mexico , Loyola-Rodrıguez, J. P. Escuela Superior de Odontologıa y Doctorado en Ciencias Biomedicas - Universidad Autonoma de Guerrero, Acapulco, GRO, Mexico , Olvera-Delgado, J. H. Faculty of Dentistry of San Luis Potosi - Universidad Autonoma de San Luis Potosı, San Luis Potosi, SLP, Mexico , Garcıa-Cortes, J. O. Faculty of Dentistry of San Luis Potosi - Universidad Autonoma de San Luis Potosı, San Luis Potosi, SLP, Mexico , Reyes-Macıas, J. F. Faculty of Dentistry of San Luis Potosi - Universidad Autonoma de San Luis Potosı, San Luis Potosi, SLP, Mexico
Pages :
5
From page :
1
To page :
5
Abstract :
Case Report. A nine-year-old patient with a diagnosis of tuberous sclerosis (with no pathological record) that showed calcifications at the brain level. Besides, the case showed the Vogt triad (epilepsy, mental retardation, and sebaceous adenoma). -e patient clinically showed a volume increase of hard consistency, without suppuration and no sessile that included the following teeth 73, 74, and 75. Cone beam computed tomography (CBCT) was obtained, and it displayed a delimited unilocular lesion. After surgical excision, the histopathological report was desmoplastic fibroma (DF). It was observed that the patient had an aggressive recurrence of DF at four months after surgery treatment. Due to these clinical findings, resective osseous surgery and curettage were carried out. It is uncommon to find these two pathologies together (DF and tuberous sclerosis). Since DF is a benign pathology but very invasive and destructive, it is necessary a constant follow-up examination due to a high recurrence frequency
Keywords :
Desmoplastic Fibroma , tuberous sclerosis , calcifications
Journal title :
Case Reports in Dentistry
Serial Year :
2018
Full Text URL :
Record number :
2616402
Link To Document :
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