The baseline 18F-FDG PET/CT imaging features in pediatric patients with congenital neuroblastoma.

IF 3.2 3区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Keyu Zhang, Guanyun Wang, Xiaoya Wang, Ying Kan, Wei Wang, Jigang Yang
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引用次数: 0

Abstract

Purpose: Congenital neuroblastoma represents a distinct subtype of neuroblastoma that originates during fetal and neonatal development. Limited research has been conducted on the prognostic significance of baseline Fluorine-18-Fluorodeoxyglucose positron emission tomography/computerized tomography (18F-FDG PET/CT) in pediatric patients with congenital neuroblastoma. This study aims to characterize the baseline 18F-FDG PET/CT imaging features in children with congenital neuroblastoma.

Methods: A retrospective collection was performed using imaging and clinical data from pediatric patients diagnosed with congenital neuroblastoma who underwent 18F-FDG PET/CT at the Beijing Friendship Hospital, Capital Medical University between June 2020 and June 2023. We collected clinical and 18F-FDG PET metabolic parameters, including maximum standardized uptake value, mean standardized uptake value (SUVmean), metabolic tumor volume (MTV), and total lesion glycolysis (TLG), total-body MTV and total-body TLG. Patients were categorized into the recurrence group and the non-recurrence group based on the follow-up outcomes.

Results: A total of 28 pediatric patients with congenital neuroblastoma were included in the study. There are 26 patients exhibited elevated serum NSE levels, 25 patients exhibited elevated serum LDH levels. Only 3 patients had MYCN amplification. 5 patients had 11q23 aberration. Primary tumors were located in the abdomen or mediastinum in all but two patients, who had pelvic and cervical involvement. All primary tumor had high FDG uptake. 6 patients had liver metastases, and 1 patient showed normal FDG uptake. 4 patients had bone marrow metastases, all of them showed high FDG uptake. With a median follow-up of 711 days, 23 patients had progression free survival, and 5 cases of recurrence.

Conclusion: Our study showed that the prognosis of congenital neuroblastoma was generally favorable and 18F-FDG PET/CT is valuable for the diagnosis and staging in congenital neuroblastoma.

小儿先天性神经母细胞瘤患者的基线18F-FDG PET/CT成像特征
目的:先天性神经母细胞瘤是一种独特的神经母细胞瘤亚型,起源于胎儿和新生儿发育期间。关于基线氟-18-氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(18F-FDG PET/CT)对先天性神经母细胞瘤患儿预后意义的研究有限。本研究旨在描述儿童先天性神经母细胞瘤的基线18F-FDG PET/CT成像特征。方法:回顾性收集2020年6月至2023年6月在首都医科大学附属北京友谊医院行18F-FDG PET/CT诊断为先天性神经母细胞瘤的儿童患者的影像学和临床资料。我们收集了临床和18F-FDG PET代谢参数,包括最大标准化摄取值、平均标准化摄取值(SUVmean)、代谢肿瘤体积(MTV)、病变总糖酵解(TLG)、全身MTV和全身TLG。根据随访结果将患者分为复发组和非复发组。结果:本研究共纳入28例先天性神经母细胞瘤患儿。26例患者血清NSE升高,25例患者血清LDH升高。仅有3例患者MYCN扩增。5例患者有11q23畸变。原发肿瘤位于腹部或纵隔,除2例患者外,均累及盆腔和宫颈。所有原发肿瘤均有高FDG摄取。6例发生肝转移,1例FDG摄取正常。4例发生骨髓转移,均呈高FDG摄取。中位随访711天,23例患者无进展生存期,5例复发。结论:我们的研究表明先天性神经母细胞瘤的预后普遍良好,18F-FDG PET/CT对先天性神经母细胞瘤的诊断和分期有一定的价值。
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来源期刊
BMC Medical Imaging
BMC Medical Imaging RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
CiteScore
4.60
自引率
3.70%
发文量
198
审稿时长
27 weeks
期刊介绍: BMC Medical Imaging is an open access journal publishing original peer-reviewed research articles in the development, evaluation, and use of imaging techniques and image processing tools to diagnose and manage disease.
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