上海交通大学学报(医学版)

• 论著(临床研究) • 上一篇    下一篇

18F-FDG PET/CT显像在儿童神经母细胞瘤分期中的价值

李佳宁,傅宏亮,冯 方,吴书其,叶智轶   

  1. 上海交通大学 医学院附属新华医院核医学科, 上海 200092
  • 出版日期:2014-06-28 发布日期:2014-06-30
  • 通讯作者: 傅宏亮, 电子信箱: fuhongliang@hotmail.com。
  • 作者简介:李佳宁(1970—), 男, 副主任医师, 硕士; 电子信箱: jianinglishanghai@aliyun.com。

Value of 18F-PET/CT imaging in staging for children with neuroblastoma

LI Jia-ning, FU Hong-liang, FENG Fang, WU Shu-qi, YE Zhi-yi   

  1. Department of Nuclear Medicine, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China
  • Online:2014-06-28 Published:2014-06-30

摘要:

目的 评价18F-FDG PET/CT在儿童神经母细胞瘤(NB)分期中的应用价值。方法 回顾性分析确诊为NB的45例患儿病例资料,按治疗前后分为治疗前组(n=13)和治疗后组(n=32)。所有患者接受18F-FDG PET/CT显像,以最大标准摄取值(SUVmax)作为PET定量分析依据。结果 治疗前组所有原发灶均见FDG摄取增高(13/13,100%),治疗后组7例FDG摄取增高(7/32,21.9%)。PET/CT检出23例淋巴结转移(23/45,51.1%),其中局部淋巴结转移17例,伴或仅远处淋巴结转移13例;骨(或骨髓)转移18例(18/45,40.0%);胸膜转移2例;肝转移1例;硬膜下转移3例;脑实质转移1例(部分患者同时存在多器官转移)。PET/CT显像后临床分期:在治疗前组中,4例分期改变(4/13,30.8%),其中1例Ⅱ期患者分期提高到Ⅳ期(1/2),3例Ⅲ期患者分期提高到Ⅳ期(3/5);在治疗后组中,17例患者分期改变17/32,53.1%),0期患者因4例发现骨(或骨髓)转移,调高分期(4/14,28.6%),可疑Ⅰ期患者中,6例因原发灶区异常软组织影未摄取FDG,调低分期(6/7,85.7%),Ⅱ期患者1例发现盆腔FDG代谢增高结节,调高分期(1/3),Ⅲ期患者中2例分别发现骨及椎管内转移,调高分期(2/2)。结论 18F-FDG PET/CT可以提供客观的分期依据,提高了NB原始分期及再分期的准确性,其中再分期获益更大;Ⅲ期患者的分期改变最为显著;治疗后Ⅰ期患者分期明显调低。PET/CT改变分期的主要原因是对全身病灶检出的敏感性高;另一方面可以评估原发灶术后术区异常组织是否具有活性。

关键词: 儿童, 神经母细胞瘤, 分期, 体层摄影术, 发射型计算机, X线计算机, 脱氧葡萄糖

Abstract:

Objective To evaluate the clinical value of 18F-FDG PET/CT in staging for children with neuroblastoma (NB). Methods The data of 45 patients who were diagnosed as NB were retrospectively analyzed. Patients were divided into the pre-treatment group (n=13) and post-treatment group (n=32). All patients underwent 18F-flourodeoxyglucose (FDG) PET/CT imaging and the maximum standardized uptake value (SUV) was used as the basis for PET quantitative analysis. Results All
patients of the pre-treatment group showed increased FDG uptake at the primary site (13/13, 100%). Seven patients of the post-treatment group showed increased FDG uptake (7/32, 21.9%). Among 23 patients who were detected with lymph nodes metastasis (23/45, 51.1%), 17 with local lymph nodes metastasis, 13 with distant lymph node metastasis, 18 with bone (or bone marrow) metastasis (18/45, 40.0%), 2 with pleura metastasis, 1 with liver metastasis, 3 with meninges metastasis, 1 with brain metastasis (some patients with multi-organ metastasis). After PET/CT imaging, stages of 4 patients of the pre-treatment group changed (4/13, 30.8%). Among them, the stage of 1 patient upgraded from II to IV (1/2), stages of 3 patients upgraded from III to IV (3/5). Stages of 17 patients of the post-treatment group changed (17/32, 53.1%). Stages of 4 stage 0 patients were upgraded due to bone (or bone marrow) metastasis (4/14, 28.6%). Among suspected stage I patients, stages of 6 patients were degraded because abnormal tissues at primary sites had no FDG uptake (6/7, 85.7%). The stage of 1 stage II patient was upgraded because nodules with FDG uptake were found in abdomen (1/3). Stages of 2 stage III patients were upgraded due to bone metastasis and intraspinal metastasis (2/2). Conclusion 18F-FDG PET/CT can provide objective evidences for staging and improve the accuracy of initial staging and re-staging for NB. Re-staging can benefit more from the PET/CT. Stages of stage III patients change more significantly. Stages of stage I patients are degraded significantly after treatments. The main reason that PET/CT can change the stage is the high sensitivity for whole body lesion detection. PET/CT can also evaluate the activity of abnormal tissues in primary sites after operations.

Key words: child, neuroblastoma, staging, tomography, emission-computed, X-ray computed, deoxyglucose