Rare Tumors
(Mar 2015)
A rare occurrence of neonatal nephroblastoma in sub-Saharan Africa: a case report and management in a resource-constrained region
Féfé Khuabi Matondo,
Aléine Nzazi Budiongo,
Bruno Muyala Tady,
Bienvenu Massamba Lebwaze,
Michel Tshikwela Lelo,
Jean Lambert Gini-Ehungu,
Idesbald Mwepu,
Emmanuel Dimbu Nkidiaka,
Michel Ntetani Aloni
Affiliations
Féfé Khuabi Matondo
Division of Hematology/Oncology and Nephrology, Department of Pediatrics, University Hospital of Kinshasa School of Medicine, University of Kinshasa
Aléine Nzazi Budiongo
Division of Hematology/Oncology and Nephrology, Department of Pediatrics, University Hospital of Kinshasa School of Medicine, University of Kinshasa
Bruno Muyala Tady
Division of Neonatology, Department of Pediatrics, University Hospital of Kinshasa School of Medicine, University of Kinshasa
Bienvenu Massamba Lebwaze
Division of Pathology, University Hospital of Kinshasa School of Medicine, University of Kinshasa
Michel Tshikwela Lelo
Division of Radiology, University Hospital of Kinshasa School of Medicine, University of Kinshasa
Jean Lambert Gini-Ehungu
Division of Hematology/Oncology and Nephrology, Department of Pediatrics, University Hospital of Kinshasa School of Medicine, University of Kinshasa
Idesbald Mwepu
Division of Pediatric Surgery, Department
of Surgery, University Hospital of Kinshasa School of Medicine, University of Kinshasa
Emmanuel Dimbu Nkidiaka
Division of Neonatology, Department of Pediatrics, University Hospital of Kinshasa School of Medicine, University of Kinshasa
Michel Ntetani Aloni
Division of Hematology/Oncology and Nephrology, Department of Pediatrics, University Hospital of Kinshasa School of Medicine, University of Kinshasa
DOI
https://doi.org/10.4081/rt.2015.5657
Journal volume & issue
Vol. 7,
no. 1
Abstract
Read online
Neonatal nephroblastoma has been rarely reported in African neonate. A premature newborn (a 5-day-old male) was transferred with a history of neonatal abdominal mass. Ultrasonography revealed 75×46 mm, well-defined mass with mixed echogenicity replacing the right kidney. The patient underwent right radical nephrectomy and the tumor was confirmed to be a blastemal predominant Wilms’ tumor by the histopathological examination and has an unfavorable prognosis. The child died secondary to multiple organ failure, three days after surgery. Our case report serves to remind us the need to bear in mind the possibility of the diagnosis of neonatal nephroblastoma in neonate with renal mass.
Keywords
Published in Rare Tumors
ISSN
2036-3605 (Print)
2036-3613 (Online)
Publisher
SAGE Publishing
Country of publisher
United Kingdom
LCC subjects
Medicine: Internal medicine: Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Website
http://journals.sagepub.com/home/rtu
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