medigraphic.com
SPANISH

Acta Pediátrica de México

Órgano Oficial del Instituto Nacional de Pediatría
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2024, Number 3

<< Back Next >>

Acta Pediatr Mex 2024; 45 (3)

Clinical and epidemiological profile of children diagnosed with neoplasms of the central nervous system in a high-level hospital

Soto MAV, Martínez SLM, Arboleda RM, Pamplona SAP, Aránzazu CAD
Full text How to cite this article

Language: Spanish
References: 30
Page: 199-208
PDF size: 233.28 Kb.


Key words:

central nervous system neoplasms, pediatrics, neoplasms, central nervous system.

ABSTRACT

Objective: to determine the clinical and epidemiological profile of the pediatric population diagnosed with central nervous system tumors attended in a high complexity hospital in Medellin, Colombia.
Materials and Methods: an observational, descriptive and retrospective study was carried out between January 2015 and December 2020, which included pediatric patients aged 0 to 14 years with a diagnosis of central nervous system tumors. For the analysis of qualitative variables, relative and absolute frequencies were measured, and for quantitative variables, measures of central tendency and interquantile ranges were used as measures of dispersion.
Results: seventy patients with clinical and/or imaging diagnosis of central nervous system tumors were included, with a median age of 9 years (minimum 0 - maximum 14 years). Male sex predominated with 57.1% and 74.3% of the population had urban origin. Regarding the characteristics of the tumor, the most common location was in the posterior fossa with 24.2%, the malignant behavior of the tumor predominated with 62.9% and 55.7% of the tumors were found in the initial stage. 87.1% (61) of the tumors were primary, 5.7% (4) presented metastasis and 20% (14) of the patients had a fatal outcome.
Conclusiones: CNS tumors are a serious oncologic disease, which considerably affects the pediatric population, with a predominance in the male sex. This study has evidenced the clinical and epidemiological profile of 52 children with CNS tumors, where the main symptoms reported at diagnosis were nausea and/or vomiting, followed by motor signs and symptoms. The main histological variant identified was neurofibromatosis type I (non-malignant), followed by medulloblastoma, which is consistent with reports in the literature. These oncologic diseases continue to have a great impact on infant mortality, as shown in several studies and also as found in this research.


REFERENCES

  1. Wong T, Ho D, Chang K, Yen S, Guo W, Chang F, et al.Primary pediatric brain tumors: statistics of Taipei VGH,Taiwan (1975-2004). Cancer. 2005;104(10):2156-67. doi:10.1002/cncr.21430.

  2. López E, González M. Tumores cerebrales infantiles, semiologíaneurológica y diagnóstico. Protoc diagn ter pediatr.2022;1:151-58.

  3. Fahmideh M, Scheurer M. Pediatric brain tumors: Descriptiveepidemiology, risk factors, and future directions.Cancer Epidemiol Biomarkers Prev. 2021;30(5):813–21.doi: 10.1158/1055-9965.

  4. Lamba N, Groves A, Torre M, Yeo K, Iorgulescu J. The epidemiologyof primary and metastatic brain tumors in infancythrough childhood. J Neurooncol. 2022;156(2):419-429.doi: 10.1007/s11060-021-03927-z.

  5. Villegas M, Ruiz N, Urdaneta L, Gutiérrez E, Vera A, BarbozaD, et al. Tumores Cerebrales Pediátricos Experiencia de 10Años. Rev venez oncol. 2013;25(2):85-97.

  6. Ostrom Q, Patil N, Cioffi G, Waite K, Kruchko C, Barnholtz-Sloan J. CBTRUS Statistical Report: Primary Brain and OtherCentral Nervous System Tumors Diagnosed in the UnitedStates in 2013-2017. Neuro Oncol. 2020:1-96. doi:10.1093/neuonc/noaa200.

  7. Tulla M, Berthold F, Graf N, Rutkowski S, Schweinitz D, SpixC, et al . Incidence, Trends, and Survival of Children withEmbryonal Tumors. Pediatrics. 2015 ;136(3):e623-32. doi:10.1542/peds.2015-0224.

  8. López-Aguilar E, Sepúlveda-Vildósola A, Rioscovian-SotoA, Pérez-Ramírez J, Siordia-Reyes G. Tumores cerebralesen pediatría. Estado actual del diagnóstico y tratamiento.Gac Mex Oncol. 2011;10(1):41-5.

  9. Berlanga P, Pasqualini C, Pötschger U, Sangüesa C, CastellaniM, Cañete A, et al . Central nervous system relapsein high-risk stage 4 neuroblastoma: The HR-NBL1/SIOPENtrial experience. Eur J Cancer. 2021;144:1-8. doi: 10.1016/j.ejca.2020.10.020.

  10. Ostrom Q, Gittleman H, Xu J, Kromer C, Wolinsky Y, KruchkoC, et al . CBTRUS statistical report: primary brain andother central nervous system tumors diagnosed in theUnited States in 2009-2013. Neuro Oncol 2016;18(5):1–75.doi:10.1093/neuonc/now27.

  11. Girardi F, Rous B, Stiller C, Gatta G, Fersht N, Storm H, et al. The histology of brain tumors for 67 331 children and 671085 adults diagnosed in 60 countries during 2000-2014:a global, population-based study (CONCORD-3). NeuroOncol. 2021 ;23(10):1765-1776. doi: 10.1093/neuonc/noab067.

  12. Sinning M. Clasificación de los tumores cerebrales. Rev.med. Clín. Las condes. 2017;28(3): 339-42. doi 10.1016/j.rmclc.2017.05.002.

  13. Wrensch M, Minn Y, Chew T, Bondy M, Berger M. Epidemiologyof primary brain tumors: current concepts andreview of the literature. Neuro Oncol. 2002;4(4):278-99.doi: 10.1093/neuonc/4.4.278.

  14. Orozco-Forero J, Martínez-Sánchez L, Pamplona-Sierra A,Rodríguez-Gázquez M, Toro-Moreno A, Álvarez-HernándezL, et al. Características clínicas y epidemiológicas de niñoscon tumores del sistema nervioso central en Medellín, Colombia.Gac Mex Oncol. 2020;19(3):79-82. doi:10.24875/j.gamo.20000368.

  15. Maaz A, Yousif T, Saleh A, Pople I, Al-Kharazi K, Al-Rayahi J,et al. Presenting symptoms and time to diagnosis for PediatricCentral Nervous System Tumors in Qatar: a report fromPediatric Neuro-Oncology Service in Qatar. Childs Nerv Syst.2021 ;37(2):465-474. doi: 10.1007/s00381-020-04815-z.

  16. Ministerio de Salud y Protección Social. Aseguramientoal Sistema General de Seguridad Social en Salud. Bogotá:MINSALUD; 2014 [citado 1 de octubre 2023]. Disponibleen: https://www.minsalud.gov.co/sites/rid/Lists/BibliotecaDigital/RIDE/VP/DOA/RL/cartillas-de-aseguramiento-alsistema-general-de-seguridadsocial-en-salud.pdf.

  17. Zapata-Tarrés M, Rivera R. Actualidades en el tratamientode los tumores del sistema nervioso central en pediatría.Acta Pediatr Mex. 2004;25(4):233-9.

  18. Alegría-Loyola M, Galnares-Olalde J, Mercado M. Tumoresdel sistema nervioso central. Rev Med Inst Mex Seguro Soc.2017;55(3):330-51.

  19. Wu X, Dangmurenjiafu G, Fan G, Zeng J, Zhao X, Sheng C,et al. Epidemiology of pediatric central nervous systemtumors in Uyghur: experience from a single center. ChildsNerv Syst. 2023 ;39(4):909-914. doi: 10.1007/s00381-022-05766-3.

  20. Suárez A, Castellanos M, Simbaqueba A, Gamboa O.Aspectos clínicos y demora para el diagnóstico en niñoscon tumores del sistema nerviosos central en el InstitutoNacional de Cancerología de Colombia. Rev Colomb Cancerol.2011;15(3):127-134.

  21. Sarmiento Limas CA. Proyecto de Consultoría y AsistenciaTécnica con la Comisión de Regulación en Salud -CRES: anexo3.1. comentarios a niveles de complejidad y actividadesde promoción de la salud y prevención de la enfermedad.Bogotá: CRES; 2009. Disponible en: https://www.minsalud.gov.co/Normatividad%20CRES/Acuerdo%2008%20de%202009%20%20Anexo%203%20%20Comentarios%20complejidad%20y%20promocion%20de%20la%20salud%2y%20prevencion%20enfermedad.pdf.

  22. Haimi M, Peretz Nahum M, Ben Arush MW. Delay in diagnosisof children with cancer: a retrospective study of 315children. Pediatr Hematol Oncol. 2004;21(1):37-48

  23. González-Paredes Y, Arreguín-González F, Páez-Aguirre S,Frías-Vázquez G, Zapata-Tarrés M. Retraso en el diagnósticoy en la referencia oportuna del niño con cáncer a uncentro especializado en atención oncológica pediátrica.Experiencia del Centro Médico Nacional “20 de Noviembre”del ISSSTE. Gaceta Mexicana de Oncología. 2014;13(1):31-38.

  24. Cecen E, Gunes D, Mutafoglu K, Sarialioglu F, Olgun N.The time to diagnosis in childhood lymphomas and othersolid tumors. Pediatr Blood Cancer. 2011;57(3):392-7. doi:10.1002/pbc.23072.

  25. Wilne S, Collier J, Kennedy C, Koller K, Grundy R, WalkerD. Presentation of childhood CNS tumours: a systematicreview and meta-analysis. Lancet Oncol. 2007;8(8):685-95.doi: 10.1016/S1470-2045(07)70207-3.

  26. Klitbo D, Nielsen R, Illum N, Wehner PS, Carlsen N. Symptomsand time to diagnosis in children with brain tumours.Dan Med Bull. 2011 ;58(7):A4285.

  27. Forjaz G, Barnholtz-Sloan J, Kruchko C, Siegel R, Negoita S,Ostrom Q, Dickie L, et al . An updated histology recode forthe analysis of primary malignant and nonmalignant brainand other central nervous system tumors in the Surveillance,Epidemiology, and End Results Program. NeurooncolAdv. 2020 ;3(1):vdaa175. doi: 10.1093/noajnl/vdaa175.

  28. Ba-Saddik I. Childhood cancer in Aden, Yemen. CancerEpidemiol. 2013 ;37(6):803-6. doi: 10.1016/j.canep.2013.10.001.

  29. Azad T, Shrestha R, Vaca S, Niyaf A, Pradhananga A, SedainG, et al . Pediatric Central Nervous System Tumorsin Nepal: Retrospective Analysis and Literature Reviewof Low- and Middle-Income Countries. World Neurosurg.2015 ;84(6):1832-7. doi: 10.1016/j.wneu.2015.07.074.

  30. Suresh S, Srinivasan A, Scott JX, Rao SM, Chidambaram B,Chandrasekar S. Profile and Outcome of Pediatric Brain Tumors- Experience from a Tertiary Care Pediatric OncologyUnit in South India. J Pediatr Neurosci. 2017 ;12(3):237-244. doi: 10.4103/jpn.JPN_31_17.




2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Acta Pediatr Mex. 2024;45