Primary Intrarenal Neuroblastoma in an Infant Mimicking Wilms Tumor: A Rare Case Report and Diagnostic Dilemma

Samuel Negash, Mesfin Wubishet Gurmu, Aneso Mohammed, Diriba Fufa Hordofa, Hailu Alemu, Melese Abere, Hawi Babu, Esubalew Mezgebu · 2026

Read Primary Intrarenal Neuroblastoma in an Infant Mimicking Wilms Tumor: A Rare Case Report and Diagnostic Dilemma by Samuel Negash, Mesfin Wubishet Gurmu, Aneso Mohammed, Diriba Fufa Hordofa, Hailu Alemu, Melese Abere, Hawi Babu, Esubalew Mezgebu (2026) in the Tower of Babel, a free online library of public-domain works preserved in clean, searchable text. No sign-up. The full text is served as a plain-text file at a predictable URL, where text is present: https://antarctic-labs.com/tower-of-babel/pmc-13241612.txt.

Description

Negash's team at Jimma report an infant whose kidney tumor wore a strong Wilms disguise. The boy, eight months old, carried a growing right-side belly mass. Scans showed a large renal tumor wrapping vessels and flecked with calcium. Those features pointed the team toward Wilms tumor.

Per protocol, chemo preceded radical kidney removal. Under the microscope, the call flipped: rosettes and neuropil marked a poorly formed neuroblastoma. Marker staining confirmed it, and neuroblastoma-directed chemo followed. The child reached full remission, but the authors urge biopsy when imaging looks atypical for Wilms. The first chemo was for Wilms.

Catalog record

CREATORSamuel Negash, Mesfin Wubishet Gurmu, Aneso Mohammed, Diriba Fufa Hordofa, Hailu Alemu, Melese Abere, Hawi Babu, Esubalew Mezgebu
YEAR2026
COLLECTIONPAPERS
FORMATTXT
FILE SIZE21 KB
VERSION1.0
LICENSECC BY 4.0
RIGHTSCC BY
SOURCEEurope PMC

Source: https://europepmc.org/articles/PMC13241612

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