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Vanished Kidney by Pheripheral Nerve Seath Tumor: A Rare Case Report
Malignant peripheral nerve-sheath tumor (MPNST) is a high-grade malignant tumor of ecto-mesenchymal origin comprising approximately 10% of soft-tissue sarcomas. They tend to occur associated with neurofibromatosis or sporadically. Here we report a MPNST at an extremely rare location and behavior cau...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830914/ https://www.ncbi.nlm.nih.gov/pubmed/24282798 http://dx.doi.org/10.5812/numonthly.8029 |
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author | Rai Bansal, Anand Singh Griwan, Mahavir Rajan Karthikeyan, Yayathi Kumar Singh, Santosh |
author_facet | Rai Bansal, Anand Singh Griwan, Mahavir Rajan Karthikeyan, Yayathi Kumar Singh, Santosh |
author_sort | Rai Bansal, Anand |
collection | PubMed |
description | Malignant peripheral nerve-sheath tumor (MPNST) is a high-grade malignant tumor of ecto-mesenchymal origin comprising approximately 10% of soft-tissue sarcomas. They tend to occur associated with neurofibromatosis or sporadically. Here we report a MPNST at an extremely rare location and behavior causing disappearance of the entire kidney. Patient evaluation included clinical, biochemical and radiological studies before treatment. Histological study revealed the rare diagnosis. Patient was asymptomatic at six-month follow-up after treatment. |
format | Online Article Text |
id | pubmed-3830914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Kowsar |
record_format | MEDLINE/PubMed |
spelling | pubmed-38309142013-11-26 Vanished Kidney by Pheripheral Nerve Seath Tumor: A Rare Case Report Rai Bansal, Anand Singh Griwan, Mahavir Rajan Karthikeyan, Yayathi Kumar Singh, Santosh Nephrourol Mon Case Report Malignant peripheral nerve-sheath tumor (MPNST) is a high-grade malignant tumor of ecto-mesenchymal origin comprising approximately 10% of soft-tissue sarcomas. They tend to occur associated with neurofibromatosis or sporadically. Here we report a MPNST at an extremely rare location and behavior causing disappearance of the entire kidney. Patient evaluation included clinical, biochemical and radiological studies before treatment. Histological study revealed the rare diagnosis. Patient was asymptomatic at six-month follow-up after treatment. Kowsar 2013-05-25 2013-07-01 /pmc/articles/PMC3830914/ /pubmed/24282798 http://dx.doi.org/10.5812/numonthly.8029 Text en Copyright © 2013, Nephrology and Urology Research Center http://creativecommons.org/licenses/by/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Rai Bansal, Anand Singh Griwan, Mahavir Rajan Karthikeyan, Yayathi Kumar Singh, Santosh Vanished Kidney by Pheripheral Nerve Seath Tumor: A Rare Case Report |
title | Vanished Kidney by Pheripheral Nerve Seath Tumor: A Rare Case Report |
title_full | Vanished Kidney by Pheripheral Nerve Seath Tumor: A Rare Case Report |
title_fullStr | Vanished Kidney by Pheripheral Nerve Seath Tumor: A Rare Case Report |
title_full_unstemmed | Vanished Kidney by Pheripheral Nerve Seath Tumor: A Rare Case Report |
title_short | Vanished Kidney by Pheripheral Nerve Seath Tumor: A Rare Case Report |
title_sort | vanished kidney by pheripheral nerve seath tumor: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830914/ https://www.ncbi.nlm.nih.gov/pubmed/24282798 http://dx.doi.org/10.5812/numonthly.8029 |
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