Pulmonary Myofibroblastic Tumour Involving the Pericardium and Left Atrium in an 18 Month Infant.

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

Abstract

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.
一例18个月婴儿肺肌成纤维细胞瘤累及心包和左心房。
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。
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