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Wilms tumor in a left pelvic kidney: A case report
INTRODUCTION: Wilms tumor(nephroblastoma) is the most common renal tumor in childhood.The most frequent anomalies and syndromes associated with this tumor involve the genitourinary tract. The occurrence of Wilms tumor with renal ectopia is rare.When present,Wilms tumor is usually found in associatio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920303/ https://www.ncbi.nlm.nih.gov/pubmed/31837612 http://dx.doi.org/10.1016/j.ijscr.2019.11.041 |
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author | Oyinloye, Adewale Olaotan Wabada, Samuel Abubakar, Auwal Mohammed Oyebanji, Lateef O. Rikin, C.U. |
author_facet | Oyinloye, Adewale Olaotan Wabada, Samuel Abubakar, Auwal Mohammed Oyebanji, Lateef O. Rikin, C.U. |
author_sort | Oyinloye, Adewale Olaotan |
collection | PubMed |
description | INTRODUCTION: Wilms tumor(nephroblastoma) is the most common renal tumor in childhood.The most frequent anomalies and syndromes associated with this tumor involve the genitourinary tract. The occurrence of Wilms tumor with renal ectopia is rare.When present,Wilms tumor is usually found in association with other forms of renal ectopia like horseshoe kidneys or crossed fused renal ectopia. However, reports of the occurrence of Wilms tumor in unilateral pelvic renal ectopia is uncommon. We report a case of Wilms tumor in a pelvic left kidney. PRESENTATION OF CASE: A 10 year old girl presented to the out-patient department with a one year history of lower abdominal mass, pain and hematuria. Examination revealed a mass in the suprapubic region. Radiological investigations showed a tumor in a left pelvic kidney. She was managed with preoperative chemotherapy, surgery and adjuvant chemotherapy. Histopathologic examination of the nephrectomy specimen confirmed the diagnosis of nephroblastoma. DISCUSSION: The occurrence of Wilms tumor in association with renal ectopia is rare. There are few reports of tumors arising in unilateral pelvic ectopic kidneys. A multi-modal treatment approach involving the use of chemotherapy, surgery and radiotherapy (for high-risk tumors) in the management of Wilms tumor gives good outcome. CONCLUSION: Tumors arising from a pelvic kidney should be considered as part of the differential diagnosis of lower abdominal masses in children. |
format | Online Article Text |
id | pubmed-6920303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-69203032019-12-26 Wilms tumor in a left pelvic kidney: A case report Oyinloye, Adewale Olaotan Wabada, Samuel Abubakar, Auwal Mohammed Oyebanji, Lateef O. Rikin, C.U. Int J Surg Case Rep Article INTRODUCTION: Wilms tumor(nephroblastoma) is the most common renal tumor in childhood.The most frequent anomalies and syndromes associated with this tumor involve the genitourinary tract. The occurrence of Wilms tumor with renal ectopia is rare.When present,Wilms tumor is usually found in association with other forms of renal ectopia like horseshoe kidneys or crossed fused renal ectopia. However, reports of the occurrence of Wilms tumor in unilateral pelvic renal ectopia is uncommon. We report a case of Wilms tumor in a pelvic left kidney. PRESENTATION OF CASE: A 10 year old girl presented to the out-patient department with a one year history of lower abdominal mass, pain and hematuria. Examination revealed a mass in the suprapubic region. Radiological investigations showed a tumor in a left pelvic kidney. She was managed with preoperative chemotherapy, surgery and adjuvant chemotherapy. Histopathologic examination of the nephrectomy specimen confirmed the diagnosis of nephroblastoma. DISCUSSION: The occurrence of Wilms tumor in association with renal ectopia is rare. There are few reports of tumors arising in unilateral pelvic ectopic kidneys. A multi-modal treatment approach involving the use of chemotherapy, surgery and radiotherapy (for high-risk tumors) in the management of Wilms tumor gives good outcome. CONCLUSION: Tumors arising from a pelvic kidney should be considered as part of the differential diagnosis of lower abdominal masses in children. Elsevier 2019-11-27 /pmc/articles/PMC6920303/ /pubmed/31837612 http://dx.doi.org/10.1016/j.ijscr.2019.11.041 Text en © 2019 The Authors. Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Oyinloye, Adewale Olaotan Wabada, Samuel Abubakar, Auwal Mohammed Oyebanji, Lateef O. Rikin, C.U. Wilms tumor in a left pelvic kidney: A case report |
title | Wilms tumor in a left pelvic kidney: A case report |
title_full | Wilms tumor in a left pelvic kidney: A case report |
title_fullStr | Wilms tumor in a left pelvic kidney: A case report |
title_full_unstemmed | Wilms tumor in a left pelvic kidney: A case report |
title_short | Wilms tumor in a left pelvic kidney: A case report |
title_sort | wilms tumor in a left pelvic kidney: a case report |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920303/ https://www.ncbi.nlm.nih.gov/pubmed/31837612 http://dx.doi.org/10.1016/j.ijscr.2019.11.041 |
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