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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...

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Autores principales: Rai Bansal, Anand, Singh Griwan, Mahavir, Rajan Karthikeyan, Yayathi, Kumar Singh, Santosh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2013
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.
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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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