ساركوما إيوينغ في الفك السفلي

Other Title(s)

Ewing sarcoma of the mandible

Joint Authors

زيناتي، مازن
درويش، خلدون

Source

مجلة جامعة دمشق للعلوم الطبية

Issue

Vol. 33, Issue 2 (31 Dec. 2017), pp.171-178, 8 p.

Publisher

Damascus University

Publication Date

2017-12-31

Country of Publication

Syria

No. of Pages

8

Main Subjects

Dental

Abstract EN

Ewing sarcoma of the mandible is rare and can be equivocal with infections or other neoplasmic lesions of dental origin.

This case report recapitulates two cases of Ewing sarcoma in the mandible, the first case is a 9-year old female affected with Ewing sarcoma in the anterior region of the mandibular body.

the second case was an 8-year-old female affected with Ewing sarcoma in the right mandibular ramus.

In both cases, a surgical resection of the tumor with safety distance was performed after preoperative chemical therapy.

The report demonstrates and compares the clinical radiographic and histopathological findings with similar cases in medical literature.

Conclusion: Ewing sarcoma rarely affects the mandible; it can show unspecific symptoms which can be suspicious with less serious lesions like odontogenic infections and benign tumors.

The early diagnosis, well timed and controlled surgical and chemical treatment play an essential role in improving the prognosis

American Psychological Association (APA)

درويش، خلدون وزيناتي، مازن. 2017. ساركوما إيوينغ في الفك السفلي. مجلة جامعة دمشق للعلوم الطبية،مج. 33، ع. 2، ص ص. 171-178.
https://search.emarefa.net/detail/BIM-930404

Modern Language Association (MLA)

درويش، خلدون وزيناتي، مازن. ساركوما إيوينغ في الفك السفلي. مجلة جامعة دمشق للعلوم الطبية مج. 33، ع. 2 (2017)، ص ص. 171-178.
https://search.emarefa.net/detail/BIM-930404

American Medical Association (AMA)

درويش، خلدون وزيناتي، مازن. ساركوما إيوينغ في الفك السفلي. مجلة جامعة دمشق للعلوم الطبية. 2017. مج. 33، ع. 2، ص ص. 171-178.
https://search.emarefa.net/detail/BIM-930404

Data Type

Journal Articles

Language

Arabic

Notes

ara

Record ID

BIM-930404