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首页> 外文期刊>Journal of Korean medical science >Embryonal rhabdomyosarcoma arising from a mediastinal teratoma: An unusual case report
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Embryonal rhabdomyosarcoma arising from a mediastinal teratoma: An unusual case report

机译:纵隔畸胎瘤引起的胚性横纹肌肉瘤:异常病例报告

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摘要

We report an unusual case of 9.5-cm-sized embryonal rhabdomyosarcoma arose from a mediastinal mature teratoma in a 46-yr-old man. A man presented with chest trauma as a result of an accident at 10 September 2011. On chest X-ray, an anterior mediastinal mass was detected. To obtain further information, chest computed tomography (CT) with contrast enhancement was performed, revealing an anterior mediastinal mass. Complete surgical excision was performed and entire specimen was evaluated. Pathologic diagnosis was embryonal rhabdomyosarcoma arising in mature cystic teratoma. After surgical excision, two cycles of dactinomycin-based chemotherapy were performed. Lung metastasis was detected on follow up CT in September 2012, and wedge resection was performed. Pathological finding of the lung lesion showed same feature with that of primary rhabdomyosarcoma.
机译:我们报告了一个不寻常的病例,该病例是由一名46岁男性的纵隔成熟畸胎瘤引起的9.5厘米大小的胚胎横纹肌肉瘤。 2011年9月10日,一名男子因交通事故而出现胸部外伤。在胸部X光片上检测到前纵隔肿块。为了获得更多的信息,进行了增强对比的胸部计算机断层扫描(CT),显示出前纵隔肿块。进行完整的手术切除并评估整个标本。病理诊断是在成熟的囊性畸胎瘤中出现胚胎横纹肌肉瘤。手术切除后,进行了两个基于放线菌素的化疗。在2012年9月的随访CT中检测到肺转移,并进行了楔形切除。肺部病变的病理表现与原发性横纹肌肉瘤相同。

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