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首页> 外文期刊>Journal of gastrointestinal cancer. >Primitive neuroectodermal tumor of the jejunum; a case report and literature review.
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Primitive neuroectodermal tumor of the jejunum; a case report and literature review.

机译:Jejunum的原始神经分区瘤; 案例报告和文献综述。

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OBJECTIVE AND IMPORTANCE: The aim of this paper is to report an unusual presentation of extranodal follicular dendritic cell tumor of neck with spinal metastasis. Follicular dendritic cells are nonlymphoid immune accessory cells present in the germinal centers of lymphoid follicles and play a crucial role in the induction and maintenance of the humoral immune response. Tumors from these cells are rare and treatment modality poorly defined. CLINICAL PRESENTATION: A 37-year-old lady presented with recurrent neck swelling which was initially reported as malignant paraganglioma. The primary disease was treated with surgery and radiotherapy. Eleven years later, the patient presented with metastasis to the spinal cord. Subsequent immunohistochemical analysis of the primary site tumor and the metastatic deposits revealed it to be a follicular dendritic cell tumor. INTERVENTION: The patient was treated with surgery followed by radiotherapy to spine, and one and half year after treatment, the patient is doing well and has regained complete motor functions. CONCLUSION: Metastasis to spinal cord for follicular dendritic cell tumor is very rare, and to the best of our knowledge, no such case has been previously reported in the scientific literature so far. In the present case, good local control was achieved with initial surgery and radiotherapy but resulted in distant failure after 11 years. This underlines the need for adjuvant systemic therapy, and understanding the biology of the tumor may help in formulating targeted therapy in the future for this rare disorder.
机译:目的和重要性:本文的目的是报告具有脊柱转移的颈部骨髓卵泡树突瘤的异常呈现。卵泡树突细胞是在淋巴卵泡的生发中心存在的非糊精免疫辅助细胞,并在诱导和维持体液免疫应答中发挥至关重要的作用。来自这些细胞的肿瘤是罕见的和治疗方式定义不足。临床介绍:一位37岁的女士患有复发性颈部肿胀,最初被报告为恶性巴拉帕氏菌瘤。主要疾病用手术和放射治疗治疗。十一年后,患者呈现出转移到脊髓。初级部位肿瘤的随后的免疫组织化学分析和转移沉积物显示出滤泡树突细胞瘤。干预:患者用手术治疗,然后进行放疗脊柱,治疗后的一年半,患者表现良好,并恢复了完整的运动功能。结论:卵泡树枝状细胞肿瘤的脊髓转移是非常罕见的,并据我们所知,迄今为止在科学文学中仍未报告这种情况。在目前的情况下,使用初始手术和放射疗法实现了良好的局部对照,但11年后导致遥远的失败。这强调了佐剂全身疗法的需要,并理解肿瘤的生物学可能有助于在未来制定终身疾病的靶向治疗。

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