Azizi Amedeo A, Slavc Irene, Theisen Benjamin Emile, Rausch Ivo, Weber Michael, Happak Wolfgang, Aszmann Oskar, Hojreh Azadeh, Peyrl Andreas, Amann Gabriele, Benkoe Thomas M, Wadsak Wolfgang, Kasprian Gregor, Staudenherz Anton, Hacker Marcus, Traub-Weidinger Tatjana
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria.
Pediatr Blood Cancer. 2018 Jan;65(1). doi: 10.1002/pbc.26733. Epub 2017 Aug 3.
About 10% of patients with neurofibromatosis type 1 (NF-1) develop malignant peripheral nerve sheath tumours (MPNST) mostly arising in plexiform neurofibroma (PN); 15% of MPNST arise in children and adolescents. 2-[ F]fluoro-2-deoxy-d-glucose ([ F]FDG)-PET (where PET is positron emission tomography) is a sensitive method in differentiating PN and MPNST in symptomatic patients with NF-1. This study assesses the value of [ F]FDG-PET imaging in detecting malignant transformation in symptomatic and asymptomatic children with PN.
Forty-one patients with NF-1 and extensive PN underwent prospective [ F]FDG imaging from 2003 to 2014. Thirty-two of the patients were asymptomatic. PET data, together with histological results and clinical course were re-evaluated retrospectively. Maximum standardised uptake values (SUVmax) and lesion-to-liver ratio were assessed.
A total of 104 examinations were performed. Mean age at first PET was 13.5 years (2.6-22.6). Eight patients had at least one malignant lesion; four of these patients were asymptomatic. Two of four symptomatic patients died, while all patients with asymptomatic malignant lesions are alive. All malignant tumours could be identified by PET imaging in both symptomatic and asymptomatic patients. All lesions judged as benign by [ F]FDG imaging and clinical judgment were either histologically benign if removed or remained clinically silent during follow-up. SUVmax of malignant and benign lesions overlapped, but no malignant lesion showed FDG uptake ≤3.15. Asymptomatic malignant lesions were detected with a sensitivity of 100%, a negative predictive value of 100% and a specificity of 45.1%.
Malignant transformation of PN also occurs in asymptomatic children and adolescents. Detection of MPNST at early stages could increase the possibility of oncologically curative resections.
1型神经纤维瘤病(NF-1)患者中约10%会发生恶性外周神经鞘瘤(MPNST),大多起源于丛状神经纤维瘤(PN);15%的MPNST发生于儿童和青少年。2-[F]氟-2-脱氧-D-葡萄糖([F]FDG)-PET(PET即正电子发射断层扫描)是鉴别有症状的NF-1患者中PN和MPNST的一种敏感方法。本研究评估[F]FDG-PET成像在检测有症状和无症状PN患儿恶性转化中的价值。
2003年至2014年,41例患有广泛PN的NF-1患者接受了前瞻性[F]FDG成像检查。其中32例患者无症状。对PET数据、组织学结果及临床病程进行回顾性重新评估。评估最大标准化摄取值(SUVmax)及病灶与肝脏比值。
共进行了104次检查。首次PET检查时的平均年龄为13.5岁(2.6 - 22.6岁)。8例患者至少有一个恶性病灶;其中4例患者无症状。4例有症状患者中有2例死亡,而所有无症状恶性病灶患者均存活。PET成像可在有症状和无症状患者中识别所有恶性肿瘤。所有经[F]FDG成像及临床判断为良性的病灶,若切除则组织学为良性,或在随访期间保持临床无症状。恶性和良性病灶的SUVmax有重叠,但无恶性病灶的FDG摄取≤3.15。无症状恶性病灶检测的灵敏度为100%,阴性预测值为100%,特异性为45.1%。
PN的恶性转化也发生于无症状儿童和青少年。早期检测MPNST可增加肿瘤根治性切除的可能性。