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Simultaneous multiple organs immature teratomas: a case report and literature review

机译:同时多器官未成熟畸胎瘤:一例报道并文献复习

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Primary simultaneous multiple organs teratomas are extremely rare. They usually arise in the gonads, and only 1–3 % of them arise in the mediastinum. We present a case of simultaneous multiple organs immature teratomas who was admitted to Razi hospital because of cough, dyspnea, and left-side supraclavicular mass. Computed tomography (CT) showed a big mass with multiple high densities, nodular, semi-solid, heterogenic structures on the left side of the neck, left-side anterior mediastinum, right-side middle mediastinum and right-side suprarenal region. CT-guided needle biopsy was performed and histopathological study showed immature teratoma. After performing neoadjuvant therapy, the tumors were removed. The patient underwent chemo radiation therapy on the mediastinum and abdomen. On 6-months follow-up, he was asymptomatic. This case is being reported because of the rarity of multiple organs immature teratomas and informing other clinicians about managing these cases.
机译:原发性多器官同时畸胎瘤非常罕见。它们通常出现在性腺中,只有1-3%发生在纵隔中。我们提出一例同时存在多器官未成熟畸胎瘤的病例,该患者由于咳嗽,呼吸困难和左侧锁骨上块肿而入院。计算机体层摄影术(CT)显示肿块较大,具有多个高密度,颈部左侧,左侧前纵隔,右侧中纵隔和右侧肾上膜上区域呈结节状,半固态,异质结构。进行了CT引导的穿刺活检,并且组织病理学研究显示未成熟的畸胎瘤。进行新辅助治疗后,将肿瘤切除。该患者对纵隔和腹部进行了化学放射治疗。在六个月的随访中,他没有症状。该病例由于多器官未成熟畸胎瘤的稀有性而被报道,并告知其他临床医生如何处理这些病例。

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