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A rare case of bilateral primary renal Burkitt lymphoma presenting with acute renal failure

Acute renal failure due to primary renal Burkitt lymphoma in children is extremely rare. We report a case with acute secondary renal failure in a 4-year-old boy who presented with abdominal pain, anorexia, and vomiting. Abdominal computed tomography scans showed bilateral nephromegaly with multiple...

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Bibliographic Details
Published in:Radiology case reports 2021-08, Vol.16 (8), p.2311-2314
Main Authors: Ninh, Tran Phan, Dinh, Truong Quang, My, Thieu-Thi Tra, Thao, Bui-Thi Phuong, Bang, Luong Viet, Duc, Nguyen Minh
Format: Article
Language:English
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Summary:Acute renal failure due to primary renal Burkitt lymphoma in children is extremely rare. We report a case with acute secondary renal failure in a 4-year-old boy who presented with abdominal pain, anorexia, and vomiting. Abdominal computed tomography scans showed bilateral nephromegaly with multiple hypoenhancing regions. Renal biopsy confirmed Burkitt lymphoma. There was no lymphadenopathy or evidence of other solid organ involvement. The patient was responsive to treatment using the EPOCH-R protocol (etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab). Here, we describe the clinical and imaging features associated with this rare entity.
ISSN:1930-0433
1930-0433
DOI:10.1016/j.radcr.2021.05.050