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儿童原发性心脏肿瘤手术:大型纤维瘤的成功治疗

Surgery for Primary Cardiac Tumors in Children: Successful Management of Large Fibromas.

作者信息

Qian Tao, Wu Zhongshi, Yang Yifeng, Xie Li, Yin Ni, Lu Ting, Huang Can, Yang Hui

机构信息

Department of Cardiovascular Surgery, The Second Xiangya Hospital of Central South University, Changsha, China.

National Health Commission Key Laboratory of Birth Defects Research, Prevention, and Treatment, Changsha, China.

出版信息

Front Cardiovasc Med. 2022 Mar 7;9:808394. doi: 10.3389/fcvm.2022.808394. eCollection 2022.

Abstract

BACKGROUND

Pediatric primary cardiac tumors (PCTs) are rare. Its clinical features and prognoses are not well defined. The management of asymptomatic patients with cardiac fibromas remains controversial.

OBJECTIVE

We aimed to examine our experience in surgical resection of pediatric PCT, with specific focuses on the management of large fibromas.

METHODS

This study included all the children who underwent surgical resection of PCT in our institution between December 2008 and June 2021. The last follow-up was performed between June 1st and August 26th, 2021. Kaplan-Meier method was used to estimate the postoperative survival, freedom from reoperation, event-free survival, and also related risk factors. The tumor volume and volume index (volume divided by body surface area) were measured for cardiac fibromas.

RESULTS

Of the 39 patients with median operative age of 9.5 [interquartile range (IQR): 1.2-16.5] years, 35 (89.7%) had benign tumors (fibromas for 15, myxomas for 13, and others for 7). The length and volume of fibromas were independent of age and symptoms (s > 0.05). The fibroma volume index was negatively correlated with age ( = 0.039), with a mean value of 105 ± 70 ml/m. Of the 15 patients with fibromas, 5 were asymptomatic, 4 received partial resection, 4 required transmural resection, and 4 presented postoperative left ventricular (LV) dysfunction (ejection fraction <50%). During the median follow-up period of 3.1 years and maximum of 12.5 years, adverse events included 2 early and 1 late death, 4 reoperations, 4 tumor recurrences, and 1 LV dysfunction lasting over one year. The 8-year survival, freedom from reoperation, and event-free survival rates were 90.4, 81.8, and 64.2%, respectively. Malignant tumor ( < 0.001) was associated with more adverse events. Transmural resection ( = 0.022) and larger tumor volume index than LV end-diastolic volume ( = 0.046) were risk factors for LV dysfunction following fibromas resection.

CONCLUSION

Pediatric surgery for PCT can be performed with low mortalities and few adverse events. The size of cardiac fibroma in children relatively decreases with the increase of age. Larger tumor volume index than LV end-diastolic volume index and transmural tumor resection predicts postoperative LV dysfunction.

摘要

背景

小儿原发性心脏肿瘤(PCTs)较为罕见。其临床特征和预后尚不明确。对于无症状心脏纤维瘤患者的治疗仍存在争议。

目的

我们旨在探讨小儿PCT手术切除的经验,特别关注大型纤维瘤的治疗。

方法

本研究纳入了2008年12月至2021年6月期间在我院接受PCT手术切除的所有儿童。末次随访于2021年6月1日至8月26日进行。采用Kaplan-Meier法评估术后生存率、再次手术-free生存率、无事件生存率以及相关危险因素。测量心脏纤维瘤的肿瘤体积和体积指数(体积除以体表面积)。

结果

39例患者的中位手术年龄为9.5岁[四分位间距(IQR):1.2 - 16.5岁],其中35例(89.7%)为良性肿瘤(15例纤维瘤、13例黏液瘤、7例其他肿瘤)。纤维瘤的长度和体积与年龄及症状无关(s>0.05)。纤维瘤体积指数与年龄呈负相关(=0.039),平均值为105±70 ml/m²。15例纤维瘤患者中,5例无症状,4例接受部分切除,4例需要全层切除,4例术后出现左心室(LV)功能障碍(射血分数<50%)。在中位随访期3.1年(最长12.5年)内,不良事件包括2例早期死亡、1例晚期死亡、4例再次手术、4例肿瘤复发以及1例持续超过1年的LV功能障碍。8年生存率、再次手术-free生存率和无事件生存率分别为90.4%、81.8%和64.2%。恶性肿瘤(<0.001)与更多不良事件相关。全层切除(=0.022)以及肿瘤体积指数大于左心室舒张末期容积(=0.046)是纤维瘤切除术后LV功能障碍的危险因素。

结论

小儿PCT手术死亡率低,不良事件少。儿童心脏纤维瘤的大小相对随年龄增长而减小。肿瘤体积指数大于左心室舒张末期容积指数以及全层肿瘤切除预示术后LV功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9964/8934860/c1cbe6de8b2a/fcvm-09-808394-g0001.jpg

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