RADIOLOGICAL APPROACH TO NEPHROBLASTOMA IN CHILDHOOD

  • Advie Memeti-Tefiku Radiology
  • Kristina Dimitrijevikj University clinic of pulmonology and allergology, Medical faculty- Skopje

Abstract

Abstract


Nephroblastoma (Wilms’ tumor) is the most common malignant kidney tumor in children, and the bilateral form occurs in approximately 5–10% of cases. It is an undifferentiated mesodermal tumor, containing a variable amount of embryonic renal elements (blastema, epithelium, and stroma).


In this paper, we present a case of a 4-year-old child with bilateral nephroblastoma, who underwent right-sided nephrectomy due to a dominant tumor mass and adjuvant chemotherapy according to the SIOP protocol. After completion of treatment, significant radiological and clinical regression of lesions in the remaining kidney was recorded. During the follow-up of several months after the end of therapy, no signs of relapse or new progression of the disease were observed.


The case emphasizes the importance of multimodal treatment and careful monitoring in patients with bilateral nephroblastoma with special emphasis on the current key role that imaging plays in preserving renal function and achieving a favorable outcome.


Keywords: nephroblastoma, bilateral, nephrectomy, regression, relapses

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Published
2025-11-25
How to Cite
MEMETI-TEFIKU, Advie; DIMITRIJEVIKJ, Kristina. RADIOLOGICAL APPROACH TO NEPHROBLASTOMA IN CHILDHOOD. Journal of Morphological Sciences, [S.l.], v. 8, n. 2, p. 257-262, nov. 2025. ISSN 2545-4706. Available at: <https://www.jms.mk/jms/article/view/vo8no2-31>. Date accessed: 30 nov. 2025.
Section
Case Report