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[儿童恶性淋巴瘤化疗后反应性胸腺增生的临床分析]

[Clinical analysis of reactive thymic hyperplasia following chemotherapy for childhood malignant lymphoma].

作者信息

Zhen Zi-Jun, Sun Xiao-Fei, Xia Yi, Wang Zhi-Hui, Ling Jia-Yu

机构信息

State Key Laboratory of Oncology in South China, Guangzhou, Guangdong 510060, P. R. China.

出版信息

Ai Zheng. 2006 Apr;25(4):471-5.

Abstract

BACKGROUND & OBJECTIVE: Reactive thymic hyperplasia following chemotherapy for malignant tumors is likely to be misdiagnosed as tumor residue or relapse, therefore, leads to unnecessary treatment. This study was to analyze the clinical features of reactive thymic hyperplasia following chemotherapy for childhood malignant lymphoma.

METHODS

Clinical data of 13 children with reactive thymic hyperplasia following chemotherapy for malignant lymphoma, treated from Mar. 1999 to Mar. 2004, were retrospectively analyzed. Of the 13 cases, 5 were Hodgkin's disease (HD), and 8 were non-Hodgkin's lymphoma (NHL). All patients received computed tomography (CT) to evaluate the therapeutic effect. When a new thymic mass emerged, positive electron tomography/computed tomography (PET/CT) was performed to identify its quality.

RESULTS

At diagnosis, 10 patients had mediastinal involvement. Reactive thymic hyperplasia occurred following the completion of chemotherapy in 9 cases, or during the maintenance of chemotherapy in 4 cases. CT showed that the longest diameters of the new mediastinal masses were 2.2-6.0 cm (mean 3.7 cm). The interval from last chemotherapy cycle to the occurrence of thymic hyperplasia was 2-12 months (mean 4 months). PET/CT was performed to 5 cases, and showed no vital tumors in the mediastinum. Three cases were misdiagnosed as tumor residue or relapse, and received second-line therapy. All patients were followed-up for 1-6 years (median 4 years), and none suffered tumor relapse.

CONCLUSIONS

Reactive thymic hyperplasia may occur following intensive chemotherapy for childhood malignant lymphoma. It should not be misdiagnosed as malignant tumors and overtreated.

摘要

背景与目的

恶性肿瘤化疗后发生的反应性胸腺增生很可能被误诊为肿瘤残留或复发,从而导致不必要的治疗。本研究旨在分析儿童恶性淋巴瘤化疗后反应性胸腺增生的临床特征。

方法

回顾性分析1999年3月至2004年3月间接受治疗的13例恶性淋巴瘤化疗后反应性胸腺增生患儿的临床资料。13例中,5例为霍奇金病(HD),8例为非霍奇金淋巴瘤(NHL)。所有患者均接受计算机断层扫描(CT)以评估治疗效果。当出现新的胸腺肿物时,进行正电子断层扫描/计算机断层扫描(PET/CT)以确定其性质。

结果

诊断时,10例患者有纵隔受累。9例反应性胸腺增生发生在化疗结束后,4例发生在化疗维持期。CT显示新的纵隔肿物最长径为2.2 - 6.0 cm(平均3.7 cm)。从最后一个化疗周期至胸腺增生发生的间隔时间为2 - 12个月(平均4个月)。5例患者进行了PET/CT检查,结果显示纵隔无活性肿瘤。3例被误诊为肿瘤残留或复发,并接受了二线治疗。所有患者随访1 - 6年(中位4年),无肿瘤复发。

结论

儿童恶性淋巴瘤强化化疗后可能发生反应性胸腺增生。不应将其误诊为恶性肿瘤并过度治疗。

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