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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237307/ https://www.ncbi.nlm.nih.gov/pubmed/34194596 http://dx.doi.org/10.1016/j.radcr.2021.05.050 |
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author | Ninh, Tran Phan Dinh, Truong Quang My, Thieu-Thi Tra Thao, Bui-Thi Phuong Bang, Luong Viet Duc, Nguyen Minh |
author_facet | Ninh, Tran Phan Dinh, Truong Quang My, Thieu-Thi Tra Thao, Bui-Thi Phuong Bang, Luong Viet Duc, Nguyen Minh |
author_sort | Ninh, Tran Phan |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8237307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-82373072021-06-29 A rare case of bilateral primary renal Burkitt lymphoma presenting with acute renal failure Ninh, Tran Phan Dinh, Truong Quang My, Thieu-Thi Tra Thao, Bui-Thi Phuong Bang, Luong Viet Duc, Nguyen Minh Radiol Case Rep Case Report 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. Elsevier 2021-06-20 /pmc/articles/PMC8237307/ /pubmed/34194596 http://dx.doi.org/10.1016/j.radcr.2021.05.050 Text en © 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Ninh, Tran Phan Dinh, Truong Quang My, Thieu-Thi Tra Thao, Bui-Thi Phuong Bang, Luong Viet Duc, Nguyen Minh A rare case of bilateral primary renal Burkitt lymphoma presenting with acute renal failure |
title | A rare case of bilateral primary renal Burkitt lymphoma presenting with acute renal failure |
title_full | A rare case of bilateral primary renal Burkitt lymphoma presenting with acute renal failure |
title_fullStr | A rare case of bilateral primary renal Burkitt lymphoma presenting with acute renal failure |
title_full_unstemmed | A rare case of bilateral primary renal Burkitt lymphoma presenting with acute renal failure |
title_short | A rare case of bilateral primary renal Burkitt lymphoma presenting with acute renal failure |
title_sort | rare case of bilateral primary renal burkitt lymphoma presenting with acute renal failure |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237307/ https://www.ncbi.nlm.nih.gov/pubmed/34194596 http://dx.doi.org/10.1016/j.radcr.2021.05.050 |
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