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Incidental giant renal oncocytoma: a case report

INTRODUCTION: Large renal oncocytomas are not very rare entities. To the best of our knowledge, we report one of the largest oncocytomas in the English literature. The tumor was incidentally diagnosed and, based on the preoperative clinical and radiographic findings, was therefore considered to be a...

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Autores principales: Anastasiadis, Anastasios, Dimitriadis, Georgios, Radopoulos, Dimitrios
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990760/
https://www.ncbi.nlm.nih.gov/pubmed/21059248
http://dx.doi.org/10.1186/1752-1947-4-358
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author Anastasiadis, Anastasios
Dimitriadis, Georgios
Radopoulos, Dimitrios
author_facet Anastasiadis, Anastasios
Dimitriadis, Georgios
Radopoulos, Dimitrios
author_sort Anastasiadis, Anastasios
collection PubMed
description INTRODUCTION: Large renal oncocytomas are not very rare entities. To the best of our knowledge, we report one of the largest oncocytomas in the English literature. The tumor was incidentally diagnosed and, based on the preoperative clinical and radiographic findings, was therefore considered to be a renal cell carcinoma. CASE PRESENTATION: A 48-year-old Caucasian diabetic man had an abdominal ultrasound for chronic abdominal discomfort, which revealed a large mass on the left kidney. An abdominal computed tomography scan revealed a contrast enhancing, well defined, heterogenous large mass (16.5 × 13.9 cm) originating from the left lower pole with cystic and solid areas. A magnetic resonance imaging scan was performed with no evidence of renal vein or caval thrombus or embolus. A radical nephrectomy was performed through a left flank intercostal incision and the pathology diagnosed renal oncocytoma. The postoperative course was uneventful and the patient was discharged six days later. CONCLUSION: Several reports have characterised this essentially benign renal histiotype, which represents 5% to 7% of all solid renal masses. Unfortunately, most renal oncocytomas cannot be differentiated from malignant renal cell carcinomas by clinical or radiographic criteria. Central stellate scar and a spoke-wheel pattern of feeding arteries are unreliable diagnostic signs and are of poor predictive value. These tumors are treated operatively with radical or partial nephrectomy or thermal ablation, depending on the clinical circumstances. We report on, to the best of our knowledge, the fourth largest lesion of this type of renal pathology.
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spelling pubmed-29907602010-11-24 Incidental giant renal oncocytoma: a case report Anastasiadis, Anastasios Dimitriadis, Georgios Radopoulos, Dimitrios J Med Case Reports Case Report INTRODUCTION: Large renal oncocytomas are not very rare entities. To the best of our knowledge, we report one of the largest oncocytomas in the English literature. The tumor was incidentally diagnosed and, based on the preoperative clinical and radiographic findings, was therefore considered to be a renal cell carcinoma. CASE PRESENTATION: A 48-year-old Caucasian diabetic man had an abdominal ultrasound for chronic abdominal discomfort, which revealed a large mass on the left kidney. An abdominal computed tomography scan revealed a contrast enhancing, well defined, heterogenous large mass (16.5 × 13.9 cm) originating from the left lower pole with cystic and solid areas. A magnetic resonance imaging scan was performed with no evidence of renal vein or caval thrombus or embolus. A radical nephrectomy was performed through a left flank intercostal incision and the pathology diagnosed renal oncocytoma. The postoperative course was uneventful and the patient was discharged six days later. CONCLUSION: Several reports have characterised this essentially benign renal histiotype, which represents 5% to 7% of all solid renal masses. Unfortunately, most renal oncocytomas cannot be differentiated from malignant renal cell carcinomas by clinical or radiographic criteria. Central stellate scar and a spoke-wheel pattern of feeding arteries are unreliable diagnostic signs and are of poor predictive value. These tumors are treated operatively with radical or partial nephrectomy or thermal ablation, depending on the clinical circumstances. We report on, to the best of our knowledge, the fourth largest lesion of this type of renal pathology. BioMed Central 2010-11-08 /pmc/articles/PMC2990760/ /pubmed/21059248 http://dx.doi.org/10.1186/1752-1947-4-358 Text en Copyright ©2010 Anastasiadis et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Anastasiadis, Anastasios
Dimitriadis, Georgios
Radopoulos, Dimitrios
Incidental giant renal oncocytoma: a case report
title Incidental giant renal oncocytoma: a case report
title_full Incidental giant renal oncocytoma: a case report
title_fullStr Incidental giant renal oncocytoma: a case report
title_full_unstemmed Incidental giant renal oncocytoma: a case report
title_short Incidental giant renal oncocytoma: a case report
title_sort incidental giant renal oncocytoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990760/
https://www.ncbi.nlm.nih.gov/pubmed/21059248
http://dx.doi.org/10.1186/1752-1947-4-358
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