纵隔淋巴结病的非典型病因:骨骼外尤文氏肉瘤

C. Elm’hadi, Mohammed Reda Khmamouche, M. Toreis, Meryem Zerrik, R. Tanz, H. Chahdi, M. Oukabli, H. Errihani, M. Ichou
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引用次数: 1

摘要

背景:尤文氏肉瘤和周围原始神经外胚层肿瘤是发生于骨骼和软组织的高度恶性肿瘤,属于尤文氏肿瘤科。原发性定位于纵隔是极其罕见的,只有少数病例报告被治疗。淋巴定位从未报道过。我们报告一例骨外尤文氏肉瘤,起源于肺门和前纵隔区域的淋巴结病变,并进行文献复习。病例介绍:一名24岁男子因持续咳嗽、夜间出汗、体重减轻6公斤而入院。胸部x线显示左肺门多环影不清。胸部计算机断层扫描证实膈上淋巴结病变在肺门和前纵隔。行活检。组织学和免疫组化分析显示肿瘤小而圆,CD99和vimentin阳性,desmine、myogenine、actin muscle lisse、Proteine S-100、Chromogranine、CD56、pancytokeratin、髓过氧化物酶和TTF1阴性。年龄小,形态学和免疫组织学特征支持Ewing组肿瘤,由于缺乏技术结构,无法进行分子细胞遗传学分析。分期阴性的任何其他转移性疾病或原始骨肿瘤,最终诊断为原发性局部尤因肉瘤纵隔淋巴结。患者接受了尤文氏肉瘤化疗方案。6个疗程后完全缓解。放疗后,同样的化疗方案持续了一年。患者在诊断后三年无局部复发或转移的迹象。结论:纵膈淋巴结病的鉴别诊断应考虑骨骼外尤文氏肉瘤。通过多模式治疗,患者是可以治愈的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Atypical Etiology of Mediastinal Lymphadenopathy: Extraskeletal Ewing Sarcoma
Background: Ewing's sarcomas and peripheral primitive neuroectodermal tumors are high grade malignant neoplasms, arising from bone and soft tissues and are grouped in the Ewing family of tumors. Primary localization in the mediastinum is extremely rare and was treated in only a few case reports. Lymphatic localization has never been reported. We present a case of an extraskeletal Ewing sarcoma arising from lymphadenopathy in the hilar and anterior mediastinal regions with literature review. Case presentation: A 24 year old man was admitted to our institution for persistent cough, nocturnal diaphoresis, and weight loss of 6 kg. The chest X-ray displayed opacity of the left hilum at polycyclic contours. Chest Computed tomography scan confirmed supradiaphragmatic lymphadenopathy in the hilar and anterior mediastinal. Biopsy was performed. Histological and immunohistochemical analysis showed small and round cells tumor with positive staining for CD99 and vimentin, and negative staining of desmine, myogenine, actine muscle lisse, Proteine S-100, Chromogranine, CD56, pancytokeratin, myeloperoxidase and TTF1. Young age, morphological and immunohistological characters argued in favor of a tumor of Ewing group .We could not perform molecular cytogenetic analysis, because of the lack of technical structure. The staging was negative for any other metastatic disease or primitive bone tumor, and final diagnosis was primary localized Ewing sarcoma in mediastinal nodes. The patient received Ewing’s sarcoma chemotherapy regimen. Complete response was achieved after six courses. Radiotherapy was prescribed, and the same chemotherapy regimen was continued totaling a period of one year. The patient was well with no evidence of local relapse or metastasis three years after diagnosis. Conclusion: Extraskeletal Ewing sarcoma should be contemplated in the differential diagnosis of mediastinal lymphadenopathy. With multimodal treatment, the patients are potentially curable.
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