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首页> 外文期刊>Journal of Medical Case Reports >Synchronously diagnosed eosinophilic granuloma and Hodgkin's disease in a 12-year-old boy: a case report
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Synchronously diagnosed eosinophilic granuloma and Hodgkin's disease in a 12-year-old boy: a case report

机译:一名12岁男孩同时诊断为嗜酸性肉芽肿和霍奇金病:一例报告

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Introduction Synchronous composite tumors are uncommon. Simultaneous, rather than metachronous or consecutive, occurrences of eosinophilic granuloma and Hodgkin's lymphoma in children are very rare. This is the first report of this kind in the medical literature. Case presentation We report the case of a 12-year-old Iranian boy with eosinophilic granuloma localized in his leg around the knee and Hodgkin's lymphoma in a cervical lymph node. The two tumours occurred synchronously before the patient had received any treatment. Conclusion Several cases of an association between eosinophilic granuloma and lymphoproliferative disorder have been reported. Some of these cases involve Hodgkin's lymphoma and Langerhans cell histiocytosis occurring in the same patient. Genetic or environmental etiologies have been postulated for eosinophilic granulomas which occur following Hodgkin's lymphomas, but have as yet not been proven. To our knowledge, synchronous occurrence of these two malignant processes in a patient who has not received any prior treatment is rare in children.
机译:简介同步性复合瘤并不常见。儿童发生嗜酸性肉芽肿和霍奇金淋巴瘤的同时而不是同步或连续发生的情况非常少见。这是医学文献中的此类首次报道。病例介绍我们报告了一个12岁的伊朗男孩,其嗜酸性肉芽肿位于膝盖周围的腿部,而霍奇金淋巴瘤位于颈部淋巴结中。在患者接受任何治疗之前,这两个肿瘤同时发生。结论已有几例嗜酸性肉芽肿与淋巴增生性疾病相关的报道。其中一些病例涉及同一患者中发生的霍奇金淋巴瘤和朗格汉斯细胞组织细胞增生症。对于霍奇金淋巴瘤之后发生的嗜酸性肉芽肿,已经提出了遗传或环境病因,但尚未得到证实。据我们所知,这两个恶性过程在未接受任何先前治疗的患者中同时发生的情况在儿童中很少见。

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