腮腺尤文氏肉瘤:罕见病例及文献综述

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2024-03-28 eCollection Date: 2024-01-01 DOI:10.1177/20363613241242570
Hayfa Chahdoura, Alia Mousli, Ghaiet El Fidaa Noubigh, Safia Yahyaoui, Rim Abidi, Nasr Chiraz
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引用次数: 0

摘要

背景:尤文氏肉瘤是一种罕见的恶性肿瘤:尤文氏肉瘤是一种罕见的恶性肿瘤。头颈部骨外尤文氏肉瘤(EES)非常罕见,而腮腺尤文氏肉瘤则更为罕见。据我们所知,在突尼斯的文献中,我们报告了首例源于腮腺的骨骼外 EES:我们报告了一例罕见的腮腺 ES 病例,患者是一名 35 岁的女性。她出现左侧腮腺肿瘤。体检发现实性固定肿块,伴有面瘫。磁共振成像显示,左侧腮腺内肿物占据整个腺体,大小为42毫米,浸润颌下肌和翼状肌。患者接受了左侧腮腺全切除术和同侧三角淋巴结清扫术。最终的病理检查和免疫组化染色证实这是一种原发性周围神经外胚层肿瘤或 PNET,60% 的肿瘤细胞存在特异性 EWING/PNET 型易位。她接受了辅助化疗(长春新碱、多柔比星、环磷酰胺与伊佛酰胺和依托泊苷交替使用四个周期),随后接受了体外放疗:每 3 个月通过宫颈核磁共振进行一次临床和放射学随访,10 个月的随访显示没有局部和远处复发。
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Ewing's sarcoma of the parotid gland: A rare entity with review of the literature.

Background: Ewing's sarcoma is a rare malignant entity. Extraosseous Ewing's sarcoma (EES) of the head and neck region is a rare occurrence, and Ewing's sarcoma of the parotid gland is even rarer. To the best of our knowledge, we reported the first case of extraskeletal ES originating from the parotid gland in the Tunisian literature.

Case report: We report a rare case of EES of the parotid gland in a 35-year-old female. She presented with left parotid tumefaction. Physical examination revealed solid and fixed mass associated with facial paralysis. Magnetic resonance imaging illustrated a left intra-parotid process occupying the entire gland measuring 42 mm infiltrating the masseter and pterygoid muscles. The patient had a total left parotidectomy with ipsilateral triangular lymph node dissection. The definitive pathological examination and the immunohistochemical staining confirmed a primary peripheral neuroectodermal tumor or PNET with the presence of a specific EWING/PNET-type translocation in 60% of the tumor cells. She had an adjuvant chemotherapy (four cycles of vincristine, doxorubicin, cyclophosphamide alternating with ifosfamide and etoposide) followed by external radiotherapy.

Conclusion: A clinical and radiological follow-up by cervical MRI was done every 3 months and The 10-month follow-up showed no locoregional and distant recurrence.

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Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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