儿童筛窦尤文氏肉瘤1例并文献复习
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Ewing sarcoma of the ethmoid sinus in children: a case and literature review
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    目的 探讨儿童鼻窦尤文肉瘤(ES)的临床特征、诊疗方法及预后。方法 回顾性分析1例筛窦ES的临床资料,并结合相关文献进行讨论。结果 该患者为原发性筛窦ES,术前诊断缺乏特异性临床表现和影像学特征。最终通过组织病理及免疫组织化学确诊。患者接受手术联合化疗、放疗的综合治疗,随访8个月无复发和转移。结论 儿童筛窦ES极罕见,临床表现无特异性,病理特征与鼻腔其他小圆细胞肿瘤相似,建议采用免疫标记物CD99+NKX2.2的方法诊断。鼻窦ES多采用综合治疗方案,预后较好。

    Abstract:

    Objective To study the clinical features, diagnosis, treatments and prognosis of Ewing sarcoma(ES) of the ethmoid sinus in children.Methods The clinical data of one case of ES were analyzed and discussed in combination with relevant literature.Results This patient had primary ethmoid ES. The preoperative diagnosis lacks specific clinical manifestations and imaging features.The final diagnosis was confirmed by histopathology and immunohistochemistry. The patient was treated with surgery combined with chemotherapy and radiotherapy, and no recurrence or metastasis after 8 months of follow-up.Conclusion Ewing sarcoma of the ethmoid sinus is extremely rare, which lacks typical and specific of clinical manifestations.The pathological features are similar to small round cells of other tumors in nasal cavity.Immunomarker CD99+NKX2.2 is recommended for diagnosis of ES. The prognosis of ES of the ethmoid sinus is better with comprehensive treatment.

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    参考文献
    [1] Negru ME, Sponghini AP, Rondonotti D, et al. Primary Ewing's sarcoma of the sinonasal tract, eroding the ethmoid and sphenoid sinus with intracranial extension:A rare case report[J]. Mol Clin Oncol, 2015, 3(4):807-810.
    [2] Lin JK, Liang J. Sinonasal Ewing sarcoma:A case report and literature review[J]. Perm J, 2018, 22:17-86.
    [3] Hafezi S, Seethala RR, Stelow EB, et al. Ewing's family of tumors of the sinonasal tract and maxillary bone[J]. Head Neck Pathol, 2011, 5(1):8-16.
    [4] 刘红刚. 鼻腔鼻窦小圆细胞恶性肿瘤的病理诊断及鉴别诊断[J]. 诊断病理学杂志, 2014, 21(7):405-409.
    [5] Thorn D, Mamot C, Krasniqi F, et al. Multimodality treatment in ewing's sarcoma family tumors of the maxilla and maxillary sinus:review of the literature[J]. Sarcoma, 2016, 2016:3872768.
    [6] Amri MF, ABdullah A, Azmi MI, et al. Primary sinonasal Ewing sarcoma:A case report[J]. Malays J Pathol, 2021, 43(2):319-325.
    [7] Bridge RS, Rajaram V, Dehner LP, et al. Molecular diagnosis of Ewing sarcoma/primitive neuroectodermal tumor in routinely processed tissue:a comparison of two FISH strategies and RT-PCR in malignant round cell tumors[J]. Mod Pathol, 2006, 19(1):1-8.
    [8] Weiss SW, Goldblum JR. Soft tissue tumors of intermediate malignancy of uncertain type. enzinger & weisss soft tissue tumors[M].5th.Philadelphia.PA:Mosby-Elsvier,2008:681-702.
    [9] Hafezi S, Seethala RR, Stelow EB, et al. Ewing's family of tumors of the sinonasal tract and maxillary bone[J]. Head Neck Pathol, 2011, 5(1):8-16.
    [10] Mccuiston A, Bishop JA. Usefulness of NKX2.2 Immunohistochemistry for distinguishing Ewing sarcoma from other sinonasal small round blue cell tumors[J]. Head Neck Pathol, 2018, 12(1):89-94.
    [11] Lin Z, Wu Z, Luo W. A novel treatment for ewing's sarcoma:chimeric antigen receptor-T cell therapy[J]. Front Immunol, 2021, 12:707211.
    [12] Grier HE, Krailo MD, Tarbell NJ, et al. Addition of ifosfamide and etoposide to standard chemotherapy for Ewing's sarcoma and primitive neuroectodermal tumor of bone[J]. N Engl J Med, 2003, 348(8):694-701.
    [13] Bosma SE, Van Driel PB, Hogendoorn PC, et al. Introducing fluorescence guided surgery into orthopedic oncology:A systematic review of candidate protein targets for Ewing sarcoma[J]. J Surg Oncol, 2018, 118(6):906-914.
    [14] Rijs Z, Jeremiasse B, Shifai N, et al. Introducing fluorescence-guided surgery for pediatric Ewing, osteo-, and rhabdomyosarcomas:A literature review[J]. Biomedicines, 2021, 9(10):1388.
    [15] Morales E, Olson M, Iglesias F, et al. Role of immunotherapy in Ewing sarcoma[J]. J Immunother Cancer, 2020, 8(2). 2020,8:e000653.
    [16] Sha HH, Wang DD, Yan DL, et al. Chimaeric antigen receptor T-cell therapy for tumour immunotherapy[J]. Biosci Rep, 2017, 37(1).
    [17] 林小龙,吕海苓,王静,等. 颈部骨外尤文氏肉瘤 1 例报道并文献 复 习[J]. 中国耳鼻咽喉颅底外科杂志,2021,27 (4):473-476.
    [18] 杨奉玲, 赵宇, 黄石, 等. 头颈部骨外尤文氏肉瘤4例并文献复习[J]. 临床耳鼻咽喉头颈外科杂志, 2013, 27(18):1000-1002,1005.
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倪涛,李超友,刘军超,刘延彬,丁永清,李燕萍,薛刚.儿童筛窦尤文氏肉瘤1例并文献复习[J].中国耳鼻咽喉颅底外科杂志,2022,28(6):111-114

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  • 收稿日期:2021-12-02
  • 在线发布日期: 2023-01-06
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