A MAXILLARY LESION WITH A RARE DIAGNOSIS; A CASE REPORT OF EWING SARCOMA

D. Tatsis, Maria Tsivilika, I. Kalaitsidou, Konstantinos Paraskevopoulos, K. Antoniades
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Abstract

Objectives Primary Ewing sarcoma of the head and neck is rare, representing only 3% of all Ewing sarcoma cases. The aim is to present a rare case of maxillary location of a Ewing sarcoma. Case report A 23-year-old male patient presented with a chief complaint of upper lip swelling attributed to a cystic lesion in the apical area left lateral maxillary incisor. Imaging showed an apical lesion of this tooth, indicating a broad osteolytic location. The lesion was removed, and a sample was taken for biopsy. The immunohistochemical findings agreed with a malignant bone tumor that exhibits features more compatible with the diagnosis of Ewing’s Sarcoma. The patient underwent chemotherapy and radiotherapy. No signs of recurrence can be seen five years after treatment. Conclusions Most of the few published cases of primary Ewing sarcoma of the maxillary have been diagnosed as cystic lesions. Early diagnosis of head and neck Ewing sarcoma is essential for operating R0 surgeries that may not require radiotherapy. Each case's severity and needs should be evaluated to select the appropriate treatment regimen.
罕见诊断的上颌病变;尤文氏肉瘤1例报告
目的原发性头颈部尤文氏肉瘤是一种罕见的肉瘤,仅占所有尤文氏肉瘤病例的3%。目的是提出一个罕见的上颌位置的尤因肉瘤的情况。病例报告一个23岁的男性患者提出了一个主要的主诉上唇肿胀归因于一个囊性病变在顶端区域左上颌外侧门牙。影像学显示牙齿的根尖病变,表明广泛的溶骨部位。切除病变,取标本进行活检。免疫组化结果与恶性骨肿瘤一致,其特征与尤文氏肉瘤的诊断更相符。病人接受了化疗和放疗。治疗后5年无复发迹象。结论少数文献报道的上颌原发性尤文氏肉瘤多数诊断为囊性病变。头颈部尤文氏肉瘤的早期诊断对于可能不需要放疗的R0手术至关重要。应评估每个病例的严重程度和需要,以选择适当的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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