Increasing abdominal circumference in children – does it require diagnosis?
Assessment of the incidence of Wilms tumor among children at the University Children’s Hospital in Lublin
DOI:
https://doi.org/10.12775/QS.2024.15.52217Keywords
wilms tumor, nephroblastoma, treatment, metastasisAbstract
Introduction and purpose: Wilms tumor, also known as nephroblastoma, is the most prevalent malignant tumor of the kidney in the pediatric population. 90% of them are diagnosed in children before the age of 6. This tumor is more common in girls, and usually occurs unilaterally. The purpose of the study is to analyse and present the incidence of the patients with Wilms tumor in University Children’s Hospital in Lublin in comparison to other studies published on PubMed.
Material and methods: The study included 34 patients with the Wilms tumor in the past medical history. They were selected among patients who had a computed tomography (CT) scan in the Department of Pediatric Radiology between November 2012 and October 2021.
Results: The average diagnostic age of Wilms tumor patients was 3 years and 9 months. The unilateral occurrence of the tumor was more common, also, the presence of a tumor in the left kidney was more frequent than in the right one. Metastases were mainly located in the lungs and liver. The less common sites of metastasis were pleural recesses and paraaortic lymph nodes. Treatment was mostly based on nephrectomy and chemotherapy, and less frequently, on radiotherapy. In the majority of patients, treatment resulted in regression of cancer lesions. Only a few recurrences of the disease were reported.
Conclusions: Successful treatment protocols for Wilms tumor (pre-operative chemotherapy and surgery) ensure a high survival rate. It is important to monitor the patient after treatment due to the risk of recurrence. During diagnostics, chest and abdominal CT should be considered because of the high incidence rate of lung and liver metastases.
References
Pater, L., Melchior, P., Rübe, C., Cooper, B. T., McAleer, M. F., Kalapurakal, J. A., & Paulino, A. C. (2021). Wilms tumor. Pediatr Blood Cancer., 68 Suppl 2, e28257.
Available from: https://doi.org/10.1002/pbc.28257
Benlhachemi, S., Abouqal, R., Coleman, N., Murray, M. J., Khattab, M., & El Fahime, E. (2023). Circulating microRNA profiles in Wilms tumour (WT): A systematic review and meta-analysis of diagnostic test accuracy. Noncoding RNA Res., 8(3), 413-425.
Available from: https://doi.org/10.1016/j.ncrna.2023.05.007
Nelson, M. V., van den Heuvel-Eibrink, M. M., Graf, N., & Dome, J. S. (2021). New approaches to risk stratification for Wilms tumor. Curr Opin Pediatr., 33(1), 40-48.
Available from: https://doi.org/10.1097/mop.0000000000000988
Modi, S., Tiang, K. W., Inglis, P., & Collins, S. (2016). Adult Wilms' Tumour: Case Report and Review of Literature. J Kidney Cancer VHL., 3(2), 1-7.
Available from: https://doi.org/10.15586%2Fjkcvhl.2016.52
Leslie, S. W., Sajjad, H., & Murphy, P. B. (2023). Wilms Tumor. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024.
Karim, A., Shaikhyzada, K., Abulkhanova, N., Altyn, A., Ibraimov, B., Nurgaliyev, D., & Poddighe, D. (2023). Pediatric Extra-Renal Nephroblastoma (Wilms' Tumor): A Systematic Case-Based Review. Cancers (Basel)., 15(9), 2563.
Available from: https://doi.org/10.3390/cancers15092563
Charlton, J., Irtan, S., Bergeron, C., & Pritchard-Jones, K. (2017). Bilateral Wilms tumour: a review of clinical and molecular features. Expert Rev Mol Med., 19, e8.
Available from: https://doi.org/10.1017/erm.2017.8
Spreafico, F., Fernandez, C. V., Brok, J., Nakata, K., Vujanic, G., Geller, J. I., Gessler, M., Maschietto, M., Behjati, S., Polanco, A., Paintsil, V., Luna-Fineman, S., & Pritchard-Jones, K. (2021). Wilms tumour. Nat Rev Dis Primers., 7(1), 75.
Available from: https://doi.org/10.1038/s41572-021-00308-8
Servaes, S. E., Hoffer, F. A., Smith, E. A., & Khanna, G. (2019). Imaging of Wilms tumor: an update. Pediatr Radiol., 49(11), 1441-1452.
Available from: https://doi.org/10.1007/s00247-019-04423-3
Theilen, T. M., Braun, Y., Bochenek, K., Rolle, U., Fiegel, H. C., & Friedmacher, F. (2022). Multidisciplinary Treatment Strategies for Wilms Tumor: Recent Advances, Technical Innovations and Future Directions. Front Pediatr., 10, 852185.
Available from: https://doi.org/10.3389/fped.2022.852185
de Carvalho, L. G., Kobayashi, T., Cypriano, M. D. S., Caran, E. M. M., Lederman, H. M., Alves, M. T. S., & Abib, S. C. V. (2021). Diagnostic Errors in Wilms' Tumors: Learning From Our Mistakes. Front Pediatr., 9, 757377.
Available from: https://doi.org/10.3389/fped.2021.757377
Cancers in children - Wilms tumor, National Cancer Registry in Poland.
Available from: https://onkologia.org.pl/pl/nowotwory-u-dzieci-guz-wilmsa-czym-jest [access: 11.03.2024]
Bhutani, N., Kajal, P., & Sharma, U. (2021). Many faces of Wilms Tumor: Recent advances and future directions. Ann Med Surg (Lond)., 64, 102202.
Available from: https://doi.org/10.1016/j.amsu.2021.102202
Key statistics for Wilms tumors, American Cancer Society.
Available from: https://www.cancer.org/cancer/types/wilms-tumor/about/key-statistics.html [access: 11.03.2024]
Vallejo Yepes, C., Bermudez, M., Camacho-Nieto, D., Mesa, J., & Bruges, R. (2021). Adult Wilms' Tumor: Case Report and Literature Review. Cureus., 13(6), e15524.
Available from: https://doi.org/10.7759/cureus.15524
PDQ Pediatric Treatment Editorial Board. Wilms Tumor and Other Childhood Kidney Tumors Treatment (PDQ®): Health Professional Version. (2024). In: PDQ Cancer Information Summaries [Internet]. Bethesda (MD): National Cancer Institute (US); 2002–.
Tołoczko-Grabarek, A., Jakubowska, A., Górski, B., Cybulski, C., Kamieńska, E., Lubiński, J., Zajączek, S., & Dębniak, T. (2002). Hereditary tumors in children - nephroblastoma. Contemporary Oncology/Współczesna Onkologia., 6(5), 300-307.
Begum, Z., Sharieff, S., & Attar, A. H. (2013). Familial occurrence of nonsyndromic wilms tumor-a report in two siblings. Indian J Surg., 75(Suppl 1), 99-102.
Available from: https://doi.org/10.1007/s12262-011-0357-8
Sze, S.K. (2021). Neonatal Renal Tumors. Clin Perinatol., 48(1), 71-81.
Available from: https://doi.org/10.1016/j.clp.2020.11.004
Spreafico, F., Biasoni, D., & Montini, G. (2024). Most appropriate surgical approach in children with Wilms tumour, risk of kidney disease, and related considerations. Pediatr Nephrol., 39(4), 1019-1022.
Available from: https://doi.org/10.1007/s00467-023-06213-4
Davidoff, A. M. (2012). Wilms tumor. Adv Pediatr., 59(1), 247-67.
Available from: https://doi.org/10.1016/j.yapd.2012.04.001
Lv, L., Yu, B., Zhai, Y., Zhao, H., Guo, R., Xu, H., & Zhang, S. (2022). Surgical removal of bilateral lung metastases from Wilms tumor via subxiphoid approach video-assisted thoracic surgery: a case report. Transl Pediatr., 11(8), 1408-1414.
Available from: https://doi.org/10.21037/tp-22-102
Artunduaga, M., Eklund, M., van der Beek, J. N., Hammer, M., Littooij, A. S., Sandberg, J. K., Schenk, J. P., Servaes, S., Singh, S., Smith, E. A., Srinavasan, A., & Khanna, G. (2023). Imaging of pediatric renal tumors: A COG Diagnostic Imaging Committee/SPR Oncology Committee White Paper focused on Wilms tumor and nephrogenic rests. Pediatr Blood Cancer., 70 Suppl 4(Suppl 4), e30004.
Available from: https://doi.org/10.1002/pbc.30004
Balis, F., Green, D. M., Anderson, C., Cook, S., Dhillon, J., Gow, K., Hiniker, S., Jasty-Rao, R., Lin, C., Lovvorn, H., MacEwan, I., Martinez-Agosto, J., Mullen, E., Murphy, E. S., Ranalli, M., Rhee, D., Rokitka, D., Tracy, EL., Vern-Gross, T., Walsh, M. F., Walz, A., Wickiser, J., Zapala, M., Berardi, R. A., & Hughes, M. (2021). Wilms Tumor (Nephroblastoma), Version 2.2021, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw., 19(8), 945-977.
Available from: https://doi.org/10.6004/jnccn.2021.0037
Linni, K., Urban, C., Lackner, H., & Höllwarth, M. E. (2003). Nephron-sparing procedures in 11 patients with Wilms' tumor. Pediatr Surg Int., 19(6), 457-62.
Available from: https://doi.org/10.1007/s00383-003-0957-x
Al-Hadidi, A., Lapkus, M., Novotny, N. M., Gowans, L. K., Chen, P. Y., & Stallion, A. (2020). Wilms Tumor with Pleural Metastasis. Glob Pediatr Health., 7, 2333794X20952292.
Available from: https://doi.org/10.1177/2333794x20952292
Vujanić, G. M., Gessler, M., Ooms, A. H. A. G., Collini, P., Coulomb-l'Hermine, A., D'Hooghe, E., de Krijger, R. R., Perotti, D., Pritchard-Jones, K., Vokuhl, C., van den Heuvel-Eibrink, M. M., & Graf, N. (2019). International Society of Paediatric Oncology–Renal Tumour Study Group (SIOP–RTSG). The UMBRELLA SIOP-RTSG 2016 Wilms tumour pathology and molecular biology protocol. Nat Rev Urol., 15(11), 693-701. Erratum in: Nat Rev Urol. 2019, 16(9), 563.
Available from: https://doi.org/10.1038%2Fs41585-018-0100-3
Vujanić, G. M., Parsons, L. N., D'Hooghe, E., Treece, A. L., Collini, P., & Perlman, E. J. (2022). Pathology of Wilms' tumour in International Society of Paediatric Oncology (SIOP) and Children's oncology group (COG) renal tumour studies: Similarities and differences. Histopathology, 80(7), 1026-1037.
Available from: https://doi.org/10.1111/his.14632
Saltzman, A. F., Cost, N. G., & Romao, R. L. P. (2023). Wilms Tumor. Urol Clin North Am., 50(3), 455-464.
Available from: https://doi.org/10.1016/j.ucl.2023.04.008
Pietras, W., Kobos, J., & Godziński, J. (2019). Standards of diagnostic and therapeutic management in kidney tumors in children. Przegląd Pediatryczny, vol. 48, no. 3, 109-111.
van den Heuvel-Eibrink, M. M., Hol, J. A., Pritchard-Jones, K., van Tinteren, H., Furtwängler, R., Verschuur, A. C., Vujanic, G. M., Leuschner, I., Brok, J., Rübe, C., Smets, A. M., Janssens, G. O., Godzinski, J., Ramírez-Villar, G. L., de Camargo, B., Segers, H., Collini, P., Gessler, M., Bergeron, C., Spreafico, F., & Graf, N. (2017). International Society of Paediatric Oncology — Renal Tumour Study Group (SIOP–RTSG). Position paper: Rationale for the treatment of Wilms tumour in the UMBRELLA SIOP-RTSG 2016 protocol. Nat Rev Urol. 2017, 14(12), 743-752.
Available from: https://doi.org/10.1038/nrurol.2017.163
Wu, X. W., Zhou, P. P., & Dong, Q. (2024). Survival assessment of nephron-sparing surgery or radical nephrectomy in children with unilateral Wilms tumor receiving adjuvant chemotherapy: a retrospective cross-sectional study. Eur Rev Med Pharmacol Sci., 28(3), 1095-1102.
Available from: https://doi.org/10.26355/eurrev_202402_35346
Taghavi, K., Sarnacki, S., Blanc, T., Boyer, O., & Heloury, Y. (2024). The rationale for nephron-sparing surgery in unilateral non-syndromic Wilms tumour. Pediatr Nephrol., 39(4), 1023-1032.
Available from: https://doi.org/10.1007/s00467-023-06099-2
Chen, H., Yang, S., & Qian, C. (2020). Effectiveness of Nephron Sparing Surgery and Radical Nephrectomy in the Management of Unilateral Wilms Tumor: A Meta-Analysis. Front Oncol., 10, 1248.
Available from: https://doi.org/10.3389/fonc.2020.01248
Lopes, R. I., & Lorenzo, A. (2017). Recent advances in the management of Wilms' tumor. F1000Res., 6, 670.
Available from: https://doi.org/10.12688/f1000research.10760.1
Niedzielska, E., Bronowicki, K., Pietras, W., Sawicz-Birkowska, K., Trybucka, K., Rąpała, M., Karpińska-Derda, I., Kurylak, A., Marciniak-Stępak, P., Panasiuk, A., Nurzyńska-Flak, J., Peregud-Pogorzelski, J., Pietrys, D., Rurańska, I., Sobol, G., Stefanowicz, J., Szymik-Kantorowicz, S., Zubowska, M., & Godziński, J. (2014). Clinical factors in relapses of Wilms' tumor--results for the Polish Pediatric Solid Tumors Study Group. Adv Clin Exp Med., 23(6), 925-31.
Available from: https://doi.org/10.17219/acem/37340
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Małgorzata Miazga, Magdalena Ostojska, Wojciech Stręk, Marianna Maślana, Aleksandra Bogoń, MD PhD Magdalena Maria Woźniak
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
Stats
Number of views and downloads: 88
Number of citations: 0