Ewing sarcoma with initial presentation in mandible: A case report

Srđan Milanović, N. Milošević, M. Dožić, D. Ristic, Goran M Stojković, N. Miletić
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Abstract

Ewing sarcoma is a tumor that rarely occurs after the age of twenty. This tumor is even more rare in the region of head and neck, either as a primary site or a place of dissemination of the disease. Treatment is multidisciplinary and includes administration of chemotherapy, surgery and/or radiotherapy. This case report refers to the 29-year-old female patient who was referred to maxillofacial surgeon for tooth pain and swelling of the left side of mandible that was not solved after the antibiotic treatment. After a biopsy was performed, Ewing's sarcoma of the mandible was diagnosed, and primary localization in the pelvis was confirmed before starting the treatment. One year after chemotherapy and radiation treatment completion, there was no sign of disease. This case shows that all doctors specialized in oral and / or maxillofacial surgery, as well as medical doctors and dentists in primary health care, have important role in early diagnosis of these rare diseases, and thus contribute to better treatment outcomes, even in advanced cases.
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以下颌骨为首发的尤文氏肉瘤1例
尤因肉瘤是一种很少发生在二十岁以后的肿瘤。这种肿瘤在头颈部区域更为罕见,无论是作为原发部位还是作为疾病传播的地方。治疗是多学科的,包括化疗、手术和/或放疗。本病例报告涉及29岁女性患者,因左侧下颌骨牙痛及肿胀,经抗生素治疗后仍未解决而转介至颌面外科。在进行活检后,下颌骨的尤文氏肉瘤被诊断出来,并在开始治疗前确认了骨盆的原发性定位。化疗和放疗完成一年后,没有任何疾病迹象。这一病例表明,所有专门从事口腔和(或)颌面外科手术的医生,以及初级卫生保健的医生和牙医,在这些罕见疾病的早期诊断方面发挥着重要作用,从而有助于改善治疗效果,即使在晚期病例中也是如此。
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审稿时长
12 weeks
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