Zhang Meihui,Jiang Dapeng.Pathogenesis and clinical characteristics of congenital neuroblastoma[J].Journal of Clinical Pediatric Surgery,2022,21(02):141-145.[doi:10.3760/cma.j.cn.101785-202105045-008]
先天性神经母细胞瘤发病机制与临床特点的研究进展
- Title:
- Pathogenesis and clinical characteristics of congenital neuroblastoma
- 关键词:
- 神经母细胞瘤/先天性; 神经母细胞瘤/病因学; 神经母细胞瘤/诊断
- Keywords:
- Neuroblastoma/CN; Neuroblastoma/ET; Neuroblastoma/DI
- 摘要:
- 神经母细胞瘤是儿童最常见的颅外实体肿瘤,来源于肾上腺髓质或交感神经节。先天性神经母细胞瘤约占神经母细胞瘤患儿总数的5%,大多数患儿于出生后1个月内确诊。与1岁以上神经母细胞瘤患儿相比,新生儿神经母细胞瘤有其独特的病程。本文就先天性神经母细胞瘤的发病机制、临床表现、治疗方法以及预测患儿长期预后的生物学因素进行综述。
- Abstract:
- As the most common extracranial solid tumor in children, neuroblastoma originates from adrenal medulla or sympathetic ganglion.Congenital neuroblastoma accounts for 5% of all neuroblastomas and most patients are diagnosed within the first month after birth.Neonates have a unique disease course as compared to children aged over 1 year.This review summarized the pathogenesis and clinical presentations of congenital neuroblastoma, as well as biological factors of predicting the long-term prognosis of congenital neuroblastoma.
参考文献/References:
[1] Fisher JPH,Tweddle DA.Neonatal neuroblastoma[J].Semin Fetal Neonatal Med,2012,17(4):207-215.DOI:10.1016/j.siny.2012.05.002.
[2] Louis CU,Shohet JM.Neuroblastoma:molecular pathogenesis and therapy[J].Annu Rev Med,2015,6(6):49-63.DOI:10.1146/annurev-med-011514-023121.
[3] Johnsen JI,Dyberg C,Wickstrom M.Neuroblastoma-a neural crest derived embryonal malignancy[J].Front Mol Neurosci,2019,12(9):9-12.DOI:10.3389/fnmol.2019.00009.
[4] Gely L,Lugo-Vicente H,Correa-Rivas M,et al.Neonatal sacrococcygeal neuroblastoma mimicking a teratoma[J].Case Rep Pediatr,2017,36(24):84-87.DOI:10.1155/2017/3624847.
[5] Haupt R,Garaventa A,Gambini C,et al.Improved survival of children with neuroblastoma between 1979 and 2005:a report of the Italian Neuroblastoma Registry[J].J Clin Oncol,2010,28(14):2331-2338.DOI:10.1200/JCO.2009.24.8351.
[6] Nuchtern JG.Perinatal neuroblastoma[J].Semin Pediatr Surg,2006,15(1):10-16.DOI:10.1053/j.sempedsurg.2005.11.003.
[7] Isaacs H Jr.Fetal and neonatal neuroblastoma:retrospective review of 271 cases[J].Fetal Pediatr Pathol,2007,26(4):177-184.DOI:10.1080/15513810701696890.
[8] French AE,Grant R,Weitzman S,et al.Folic acid food fortification is associated with a decline in neuroblastoma[J].Clin Pharmacol Ther,2003,74(3):288-294.DOI:10.1016/S0009-9236(03)00200-5.
[9] Davidoff AM.Neonatal neuroblastoma[J].Clin Perinatol,2021,48(1):101-115.DOI:10.1016/j.clp.2020.11.006.
[10] Sim?es-Costa M,Bronner ME.Establishing neural crest identity:a gene regulatory recipe[J].Development,2015,142(2):242-257.DOI:10.1242/dev.105445.
[11] Mundell NA,Labosky PA.Neural crest stem cell multipotency requires Foxd3 to maintain neural potential and repress mesenchymal fates[J].Development,2011,138(4):641-652.DOI:10.1242/dev.054718.
[12] Westermann F,Muth D,Benner A,et al.Distinct transcriptional MYCN/c-MYC activities are associated with spontaneous regression or malignant progression in neuroblastomas[J].Genome Biol,2008,9(10):472-480.DOI:10.1186/gb-2008-9-10-r150.
[13] 唐湘莲,刘登辉,黎明,等.miR-29b对神经母细胞瘤增殖、侵袭和转移的影响研究[J].临床小儿外科杂志,2020,19(8):711-716.DOI:10.3969/j.issn.1671-6353.2020.08.010. Tang XL,Liu DH,Li M,et al.Effect of mir-29b upon the proliferation,invasion and migration of neuroblastoma cells[J].J Clin Ped Sur,2020,19(8):711-716.DOI:10.3969/j.issn.1671-6353.2020.08.010.
[14] Trigg RM,Turner SD.ALK in neuroblastoma:biological and therapeutic implications[J].Cancers (Basel),2018,10(4):113-117.DOI:10.3390/cancers10040113.
[15] Pei D,Luther W,Wang W,et al.Distinct neuroblastoma-associated alterations of PHOX2B impair sympathetic neuronal differentiation in zebrafish models[J].PLoS Genet,2013,9(6):33-35.DOI:10.1371/journal.pgen.1003533.
[16] Tonini GP,Capasso M.Genetic predisposition and chromosome instability in neuroblastoma[J].Cancer Metastasis Rev,2020,39(1):275-285.DOI:10.1007/s10555-020-09843-4.
[17] Carén H,Kryh H,Nethander M,et al.High-risk neuroblastoma tumors with 11q-deletion display a poor prognostic,chromosome instability phenotype with later onset[J].Proc Natl Acad Sci USA,2010,107(9):4323-4328.DOI:10.1073/pnas.0910684107.
[18] Westermann F,Schwab M.Genetic parameters of neuroblastomas[J].Cancer Lett,2002,184(2):127-147.DOI:10.1016/s0304-3835(02)00199-4.
[19] Psarris A,Sindos M,Dimopoulou A,et al.Prenatal diagnosis of adrenal neuroblastoma-differential diagnosis of suprarenal masses in the third trimester of pregnancy[J].Ultrasound Int Open,2019,5(3):E93-E95.DOI:10.1055/a-1070-8651.
[20] Kushner BH.Neuroblastoma:a disease requiring a multitude of imaging studies[J].J Nucl Med,2004,45(7):1172-1188.
[21] Hwang SM,Yoo SY,Kim JH,et al.Congenital adrenal neuroblastoma with and without cystic change:differentiating features with an emphasis on the of value of ultrasound[J].AJR Am J Roentgenol,2016,207(5):1105-1111.DOI:10.2214/AJR.16.16452.
[22] Nuchtern JG,London WB,Barnewolt CE,et al.A prospective study of expectant observation as primary therapy for neuroblastoma in young infants:a Children’s Oncology Group study[J].Ann Surg,2012,256(4):573-580.DOI:10.1097/SLA.0b013e31826cbbbd.
[23] Singh H,Mohan C,Mohindroo NK,et al.Cervical neuroblastoma[J].Indian J Otolaryngol Head Neck Surg,2007,59(3):288-290.DOI:10.1007/s12070-007-0083-5.
[24] Tai CF,Lee KS,Chen IH.Primary cervical neuroblastoma in infants[J].Formos Med Assoc,1997,96(7):561-564.
[25] Schleiermacher G,Rubie H,Hartmann O,et al.Neuroblastoma study group of the French Society of Paediatric Oncology.treatment of stage 4s neuroblastoma-report of 10 years’ experience of the French Society of Paediatric Oncology (SFOP)[J].Br J Cancer,2003,89(3):470-476.DOI:10.1038/sj.bjc.6601154.
[26] Whittle SB,Smith V,Doherty E,et al.Overview and recent advances in the treatment of neuroblastoma[J].Expert Rev Anticancer Ther,2017,17(4):369-386.DOI:10.1080/14737140.2017.1285230.
[27] Swift CC,Eklund MJ,Kraveka JM,et al.Updates in diagnosis,management,and treatment of neuroblastoma[J].Radiographics,2018,38(2):566-580.DOI:10.1148/rg.2018170132.
[28] Gupta R,Mala TA,Mathur P,et al.Stage 4S Bilateral adrenal neuroblastoma in a newborn[J].APSP J Case Rep,2014,5(1):9.
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备注/Memo
收稿日期:2021-05-24。
基金项目:国家临床重点专科项目资助
通讯作者:姜大朋,Email:jdp509@163.com