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ArticleRadiology case reports2025

Pediatric renal rhabdoid tumor: Imaging features and diagnostic challenges of a rare and aggressive neoplasm.

K Elaitari, N Boujida, S Jabour, K Maslouhi, N Allali, L Chat, M Ochan, M Kisra, M El Kababri, A Kili and 2 more

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Article in Radiology case reports, 2025. 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

K ElaitariDepartment of Radiology, Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
N BoujidaDepartment of Radiology, Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
S JabourDepartment of Radiology, Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
K MaslouhiDepartment of Radiology, Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
N AllaliDepartment of Radiology, Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
L ChatDepartment of Radiology, Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
M OchanPediatric Surgery Department "A" Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
M KisraPediatric Surgery Department "A" Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
M El KababriDepartment of Pediatric Hematology and Oncology, Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
A KiliDepartment of Pediatric Hematology and Oncology, Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.
N Lamalmi16 November Center of Pathological Anatomy and Cytology, Rabat, Morocco.
S El HaddadDepartment of Radiology, Children's Hospital, Ibn Sina University Hospital Center, Rabat, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The renal rhabdoid tumor is an extremely rare pediatric tumor, accounting for approximately 2% of renal tumors in children. It occurs in 80% of cases before the age of 2 years and is considered the most aggressive malignant renal tumor, with a particularly poor prognosis. It must be distinguished from Wilms tumor, the most common pediatric renal tumor. The case we report is characterized by a radiological presentation that is not suggestive of this tumor entity. Due to the overlap of clinical and radiological features with other types of renal tumors, histological confirmation is essential for any renal mass with atypical clinical or radiological presentation.

Indexed as

HistologyImagingManagementRenal rhabdoid tumor

Identifiers

PMID41050899
PMCPMC12493216

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