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Imaging of Renal Medullary Carcinoma
Renal medullary carcinoma (RMC) is a rare, highly aggressive tumor recognized as an independent pathological entity. African-descent adolescents and young adults with sickle cell hemoglobinopathy are the most affected groups. This rare subtype of renal cell carcinoma has its own morphogenetic and pa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Codon Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364331/ https://www.ncbi.nlm.nih.gov/pubmed/28405543 http://dx.doi.org/10.15586/jkcvhl.2017.62 |
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author | Greco, Federico Faiella, Eliodoro Santucci, Domiziana Mallio, Carlo Augusto Nezzo, Marco Quattrocchi, Carlo Cosimo Beomonte Zobel, Bruno Grasso, Rosario Francesco |
author_facet | Greco, Federico Faiella, Eliodoro Santucci, Domiziana Mallio, Carlo Augusto Nezzo, Marco Quattrocchi, Carlo Cosimo Beomonte Zobel, Bruno Grasso, Rosario Francesco |
author_sort | Greco, Federico |
collection | PubMed |
description | Renal medullary carcinoma (RMC) is a rare, highly aggressive tumor recognized as an independent pathological entity. African-descent adolescents and young adults with sickle cell hemoglobinopathy are the most affected groups. This rare subtype of renal cell carcinoma has its own morphogenetic and pathological characteristics. The major clinical manifestations include gross hematuria, abdominal or flank pain, and weight loss. The prognosis is very poor, with 95% of cases diagnosed at an advanced stage of the disease. In this review, we summarize the morphologic and dynamic characteristics of RMC under various imaging modalities such as ultrasound, computed tomography, and magnetic resonance. Differential diagnosis and management strategies are also discussed. |
format | Online Article Text |
id | pubmed-5364331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Codon Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-53643312017-04-12 Imaging of Renal Medullary Carcinoma Greco, Federico Faiella, Eliodoro Santucci, Domiziana Mallio, Carlo Augusto Nezzo, Marco Quattrocchi, Carlo Cosimo Beomonte Zobel, Bruno Grasso, Rosario Francesco J Kidney Cancer VHL Review Article Renal medullary carcinoma (RMC) is a rare, highly aggressive tumor recognized as an independent pathological entity. African-descent adolescents and young adults with sickle cell hemoglobinopathy are the most affected groups. This rare subtype of renal cell carcinoma has its own morphogenetic and pathological characteristics. The major clinical manifestations include gross hematuria, abdominal or flank pain, and weight loss. The prognosis is very poor, with 95% of cases diagnosed at an advanced stage of the disease. In this review, we summarize the morphologic and dynamic characteristics of RMC under various imaging modalities such as ultrasound, computed tomography, and magnetic resonance. Differential diagnosis and management strategies are also discussed. Codon Publications 2017-03-21 /pmc/articles/PMC5364331/ /pubmed/28405543 http://dx.doi.org/10.15586/jkcvhl.2017.62 Text en Copyright © 2016 Codon Publications License: This open access article is licensed under Creative Commons Attribution 4.0 International (CC BY 4.0). http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Review Article Greco, Federico Faiella, Eliodoro Santucci, Domiziana Mallio, Carlo Augusto Nezzo, Marco Quattrocchi, Carlo Cosimo Beomonte Zobel, Bruno Grasso, Rosario Francesco Imaging of Renal Medullary Carcinoma |
title | Imaging of Renal Medullary Carcinoma |
title_full | Imaging of Renal Medullary Carcinoma |
title_fullStr | Imaging of Renal Medullary Carcinoma |
title_full_unstemmed | Imaging of Renal Medullary Carcinoma |
title_short | Imaging of Renal Medullary Carcinoma |
title_sort | imaging of renal medullary carcinoma |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364331/ https://www.ncbi.nlm.nih.gov/pubmed/28405543 http://dx.doi.org/10.15586/jkcvhl.2017.62 |
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