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1.
Cranio ; 38(5): 333-341, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-30296919

RESUMEN

OBJECTIVES: This study aimed to evaluate and report the outcomes associated with the management of patients who were treated surgically for medication-related osteonecrosis of the jaw (MRONJ).Methods: Demographic and medical profiles of patients with a diagnosis of MRONJ were created. The type of surgical treatment, complications, and treatment outcomes were identified.Results: Twenty-one patients with an average age of 68.42 years (range 40-90 years) were included. Nineteen patients had only mandible involvement, one patient had only maxilla involvement, and one patient had both mandible and maxilla involvement. Thirteen patients underwent marginal resections. Eight patients underwent segmental resection of the mandible with immediate reconstruction. Nineteen patients healed without any complications. Two patients who had undergone segmental resection of the mandible experienced postoperative complications and needed a second surgery to achieve primary closure.Discussion: Advanced MRONJ can effectively be treated with resective surgery in combination with medical treatment.


Asunto(s)
Osteonecrosis de los Maxilares Asociada a Difosfonatos , Conservadores de la Densidad Ósea , Osteonecrosis , Adulto , Anciano , Anciano de 80 o más Años , Humanos , Mandíbula , Maxilar , Persona de Mediana Edad , Resultado del Tratamiento
2.
J Oral Maxillofac Surg ; 74(11): 2229.e1-2229.e4, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27425882

RESUMEN

Fibrous dysplasia (FD) is a benign fibro-osseous lesion that typically behaves as a painless, slowly expanding tumor. On rare occasion, FD will undergo malignant transformation. When sarcomatous change occurs, osteosarcoma is the typical variant, followed by chondrosarcoma and fibrosarcoma. The incidence of malignant change varies from 1 to 4% depending on whether the disease is mono-ostotic or polyostotic and syndromic (McCune-Albright or Jaffe-Lichtenstein syndrome). Despite the low incidence of malignant change, the potential lethality of this disease behooves treating surgeons to be keenly aware of the signs and symptoms indicative of malignancy. This report documents a case of spontaneous transformation of FD into osteosarcoma in the setting of longstanding craniomaxillofacial FD in a 39-year-old woman.


Asunto(s)
Displasia Fibrosa Poliostótica/patología , Neoplasias Mandibulares/patología , Osteosarcoma/patología , Lesiones Precancerosas/patología , Adulto , Transformación Celular Neoplásica , Femenino , Displasia Fibrosa Poliostótica/diagnóstico , Humanos , Neoplasias Mandibulares/diagnóstico , Osteosarcoma/diagnóstico , Lesiones Precancerosas/diagnóstico
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