Evidence map›Paper›PMID 42905326›Full record

ArticlePediatric surgery international2026

Relative frequency of non-Wilms renal tumours in children: an institutional experience from a national tertiary referral centre in Malaysia.

Mohd Yusran Othman, Nik Muhammad Lukman Nik Ab Aziz, John Emmanuel Gilbert Fernandez, Kok Hoi Teh, Rohazly Ismail, Hui Hui Siah, Mohd Yusof Abdullah, Zakaria Zahari

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Article in Pediatric surgery international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Mohd Yusran OthmanDepartment of Paediatric Surgery, Hospital Tunku Azizah (Ministry of Health), Kuala Lumpur, Malaysia. yusranothman@gmail.com.ORCID https://orcid.org/0000-0001-7673-9029
Nik Muhammad Lukman Nik Ab AzizDepartment of Pathology, Hospital Tunku Azizah (Ministry of Health), Kuala Lumpur, Malaysia.
John Emmanuel Gilbert FernandezDepartment of Paediatric Surgery, Hospital Tunku Azizah (Ministry of Health), Kuala Lumpur, Malaysia.
Kok Hoi TehPaediatric Haemato-Oncology Unit, Department of Paediatrics, Hospital Tunku Azizah (Ministry of Health), Kuala Lumpur, Malaysia.
Rohazly IsmailDepartment of Radiology, Hospital Tunku Azizah (Ministry of Health), Kuala Lumpur, Malaysia.
Hui Hui SiahDepartment of Pathology, Hospital Kuala Lumpur (Ministry of Health), Kuala Lumpur, Malaysia.
Mohd Yusof AbdullahDepartment of Paediatric Surgery, Hospital Tunku Azizah (Ministry of Health), Kuala Lumpur, Malaysia.
Zakaria ZahariDepartment of Paediatric Surgery, Hospital Tunku Azizah (Ministry of Health), Kuala Lumpur, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeInternational protocols for paediatric renal tumours are largely based on Western data with Wilms tumour (WT) accounting for more than 90% of cases. We aimed to evaluate the relative frequency of WT and Non-Wilms Renal Tumours (NWRTs) in a diverse Asian cohort in Malaysia.

methodsA retrospective review was conducted of all primary paediatric renal tumours treated at a national tertiary referral centre from 2015 to 2024. Diagnosis was confirmed via post-operative histopathology.

resultsOf 95 children (median age 29 months), all were Asian descent (73.7% Malay, 9.5% Chinese, 6.3% Indian). WT accounted for only 68.4% of cases, while NWRTs accounted for 31.6%. Among NWRTs, 63.3% were malignant, primarily clear cell sarcoma of the kidney (CCSK, n = 7) and renal cell carcinoma (RCC, n = 4). In the classic WT age range (6-84 months), WT prevalence was only 75.6%, with CCSK representing 9.0%. Congenital mesoblastic nephroma (CMN) predominated in infants < 6 months (71.4%), while RCC was exclusively seen in children > 84 months (40.0%).

conclusionThe substantial proportion of malignant NWRTs observed in this institutional cohort highlights potential risks of neoadjuvant chemotherapy without histological confirmation. Histopathological diagnosis via percutaneous core-needle biopsy or primary surgery may be highly considered in similar clinical settings.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsSarcoma, Clear CellWilms TumorChildChild, PreschoolFemaleHumansInfantMalaysiaMalePrevalenceRetrospective StudiesTertiary Care CentersAsian childrenNon-Wilms renal tumoursPaediatric surgical oncologyWilms tumour

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