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Tubulocystic Carcinoma of the Kidney: A Case Report of Natural History and Long-Term Follow-Up
Tubulocystic carcinoma (TC) is a rare primary renal tumor that has been recently described in the pathology literature. Formerly termed low-grade collecting duct carcinoma, further molecular analysis has shown TC to be a distinct entity that is separate from the more aggressive collecting duct carci...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
TheScientificWorldJOURNAL
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763676/ https://www.ncbi.nlm.nih.gov/pubmed/20364244 http://dx.doi.org/10.1100/tsw.2010.56 |
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author | Moses, Kelvin A. DeCaro, John J. Osunkoya, Adeboye O. Issa, Muta M. |
author_facet | Moses, Kelvin A. DeCaro, John J. Osunkoya, Adeboye O. Issa, Muta M. |
author_sort | Moses, Kelvin A. |
collection | PubMed |
description | Tubulocystic carcinoma (TC) is a rare primary renal tumor that has been recently described in the pathology literature. Formerly termed low-grade collecting duct carcinoma, further molecular analysis has shown TC to be a distinct entity that is separate from the more aggressive collecting duct carcinoma. Previous series have described the microscopic and immunohistochemical features of this tumor. We describe the natural history of this tumor in a patient who was followed with active surveillance for several years and then underwent partial nephrectomy. Long-term follow-up has shown no evidence of disease. A review of the pertinent literature is performed. |
format | Online Article Text |
id | pubmed-5763676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | TheScientificWorldJOURNAL |
record_format | MEDLINE/PubMed |
spelling | pubmed-57636762018-06-03 Tubulocystic Carcinoma of the Kidney: A Case Report of Natural History and Long-Term Follow-Up Moses, Kelvin A. DeCaro, John J. Osunkoya, Adeboye O. Issa, Muta M. ScientificWorldJournal Case Study Tubulocystic carcinoma (TC) is a rare primary renal tumor that has been recently described in the pathology literature. Formerly termed low-grade collecting duct carcinoma, further molecular analysis has shown TC to be a distinct entity that is separate from the more aggressive collecting duct carcinoma. Previous series have described the microscopic and immunohistochemical features of this tumor. We describe the natural history of this tumor in a patient who was followed with active surveillance for several years and then underwent partial nephrectomy. Long-term follow-up has shown no evidence of disease. A review of the pertinent literature is performed. TheScientificWorldJOURNAL 2010-04-01 /pmc/articles/PMC5763676/ /pubmed/20364244 http://dx.doi.org/10.1100/tsw.2010.56 Text en Copyright © 2010 Kelvin A. Moses et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Study Moses, Kelvin A. DeCaro, John J. Osunkoya, Adeboye O. Issa, Muta M. Tubulocystic Carcinoma of the Kidney: A Case Report of Natural History and Long-Term Follow-Up |
title | Tubulocystic Carcinoma of the Kidney: A Case Report of Natural History and Long-Term Follow-Up |
title_full | Tubulocystic Carcinoma of the Kidney: A Case Report of Natural History and Long-Term Follow-Up |
title_fullStr | Tubulocystic Carcinoma of the Kidney: A Case Report of Natural History and Long-Term Follow-Up |
title_full_unstemmed | Tubulocystic Carcinoma of the Kidney: A Case Report of Natural History and Long-Term Follow-Up |
title_short | Tubulocystic Carcinoma of the Kidney: A Case Report of Natural History and Long-Term Follow-Up |
title_sort | tubulocystic carcinoma of the kidney: a case report of natural history and long-term follow-up |
topic | Case Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763676/ https://www.ncbi.nlm.nih.gov/pubmed/20364244 http://dx.doi.org/10.1100/tsw.2010.56 |
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