一例18个月婴儿肺肌成纤维细胞瘤累及心包和左心房。

R. Lamas-Pinheiro, G. Rodesch, C. Devalck, V. Segers, K. Khelif, M. Cappello, H. Steyaert
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引用次数: 4

摘要

炎症性肌纤维母细胞瘤(IMT)是儿童最常见的原发性肺肿瘤,它可能具有局部侵袭性。在一个18个月大的女婴局部进展肺IMT的管理提出。一位患有持续性全身性炎症综合征的儿童,在计算机断层扫描(CT)中偶然发现左肺肿块。活检证实了诊断;术前皮质治疗后,行左侧全肺切除术。心包和左心房被侵犯和切除,需要心包重建。随访四年无复发。类固醇在肿瘤缩小中起作用,但边缘切除是金标准。扩展的方法是可行的,并且在晚期病例中经常需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulmonary Myofibroblastic Tumour Involving the Pericardium and Left Atrium in an 18 Month Infant.
Inflammatory myofibroblastic tumor (IMT) is the most frequent primary lung tumor in children and it may be locally aggressive. The management of a locally advanced pulmonary IMT in an 18 month-old female child is presented.A left pulmonary mass was incidentally found on the computerized tomography (CT) scan of a child with persistent systemic inflammatory syndrome. Biopsy confirmed the diagnosis; after preoperative corticotherapy, left pneumonectomy was performed. The pericardium and left atrium were invaded and resected, requiring pericardial reconstruction. There is no relapse at four years of follow-up.Steroids play a role in tumor size reduction, but marginal resection is the gold standard. Extended approaches are feasible and often required in advanced cases.
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