Ewing's sarcoma of the mandible occurs rarely; there have been less than 50 reported cases in the past 30 years and none of these have been in the otolaryngologic literature. They usually present in the second decade of life with pain and swelling of the soft tissue overlying the mandible. The diagnosis can only be made by an adequate mandibular biopsy, although x-rays and clinical presentation are helpful. Current treatment consists of radiation therapy and sequential adjuvant chemotherapy.
Get full access to this article
View all access options for this article.
References
1.
EwingJ: Diffuse endothelioma of bone. New York Path Soc21: 17–24, 1921.
2.
DahlinDCCoventryMDScanlonPW: A critical analysis of 165 cases. J Bone Joint Surg43A: 185–92, 1961.
3.
BrownsonRJCookRP: Ewing's sarcoma of the maxilla. Ann Otol Rhinol Laryngol78: 1299–1303, 1969.
4.
PotdarGG: Ewing's tumors of the jaws. Oral Surg29: 505–12, 1970.
5.
RosenG: Management of malignant bone tumors in children and adolescents. Pediatr Clin North Amer183–201, Feb 1976.
6.
KellyJRBarrES: Ewing's sarcoma with involvement of the head and neck. J Dent Child18: 43–6, 1976.
7.
RocaANSmithJLMacCombWS: Ewing's sarcoma of the maxilla and mandibule. Oral Surg25: 194–203, 1968.
8.
SpjutHJ: Tumors of Bone and Cartilage. Atlas of Tumor Pathology, Second Series, Fascicle 5. Armed Forces Institute of Pathology, Washington, D. C., 1971, pp 216–229.
9.
RosenGWollnerNTanC: Disease-free survival in children with Ewing's sarcoma treated and radiation therapy and adjuvant four-drug sequential chemotherapy. Cancer33: 384–93, 1974.
10.
JohnsonREPomeroyTC: Evaluation of therapeutic results in Ewing's sarcoma. Am J Roentgenol123: 583–87, 1975.